US3708505A - Process for preparation of d,l-alpha tocopherol - Google Patents

Process for preparation of d,l-alpha tocopherol Download PDF

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US3708505A
US3708505A US00119048A US3708505DA US3708505A US 3708505 A US3708505 A US 3708505A US 00119048 A US00119048 A US 00119048A US 3708505D A US3708505D A US 3708505DA US 3708505 A US3708505 A US 3708505A
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acid
mole
alpha
strong
combined
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US00119048A
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S Greenbaum
W Hacke
H Horn
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NUTRIUS Inc A CORP OF
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Diamond Shamrock Corp
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • C07D311/70—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with two hydrocarbon radicals attached in position 2 and elements other than carbon and hydrogen in position 6
    • C07D311/72—3,4-Dihydro derivatives having in position 2 at least one methyl radical and in position 6 one oxygen atom, e.g. tocopherols

Definitions

  • D,l-alpha-tocopherol is prepared by reacting trimethylhydroquinone (TMHQ) and isophytol in the presence of a combined acid condensation agent which comprises a Lewis acid and at least one strong acid, which combined acids act in a synergistic manner.
  • TMHQ trimethylhydroquinone
  • a typical example of a usefulLewis acid is zinc chloride.
  • Typical examples of strong acids are p-toluene sulfonic acid and sodium bisulfate.
  • the preparation of d,l-alpha-tocopl1erol by the condensation of trimethylhydroquinone and phytol or derivatives thereof in the presence of solvents and an acid condensing agent is well known in the art.
  • the acid catalyst used in the prior art may be either a Lewis acid such as zinc chloride, boron tribromide, etc., or strong inorganic acids such as sulfuric acid, hydrochloric acid, etc., or strong organic acids such as p-toluene sulfonic acid.
  • acetic anhydride may be added to produce d,l-alpha-tocopheryl acetate. It is an advantage of the present process that the synthesis is essentially a one-step process and that a yield of high quality d,l-alpha-tocopherol is produced.
  • the phytol may be phytol, isophytol, phytadiene, phytyl chloride, phytyl bromide, phytyl acetate, phytyl methyl ether, phytol derivatives, substituted phytol, and the like.
  • the preferred phytol is isophytol.
  • Inert organic solvents which may be employed in the present invention are those solvents boiling below the boiling points of the reactants and the desired product.
  • Suitable inert solvents include the aliphatic hydrocarbon solvents of to 12 carbon atoms, or more, as for example, n-heptane; carboxylic acids having 2 to 6 carbon atoms such as acetic acid, propionic acid, butanoic acid, and
  • hexanoic acid hexanoic acid
  • aromatic solvents such as xylene, benzene, and toluene
  • ethers such as isopropyl ether, dioxane, tetrahydrofuran; and the like.
  • the acid condensation catalyst of this invention must consist of a combination of two acids, one of which must be a Lewis acid and the other a strong acid which may be organic or inorganic.
  • Suitable Lewis acids include boron trifluoride, boron tribromide, aluminum chloride, aluminum bromide, zinc chloride, boron trifluorodiphosphoric acid complex, and the like.
  • the preferred Lewis acid is zinc chloride.
  • Suitable strong acids include sulfuric acid, hydrochloric acid, nitric acid, para-toluene sulfonic acid, sodium bisulfate, mixtures thereof, and the like.
  • Preferred strong acids are sulfuric acid, para-toluene sulfonic acid and sodium bisulfate.
  • An especially preferred strong acid is sodium bisulfate.
  • the ratio of ingredients is from about 0.9 to 1.1 mole (and preferably about 1.0 mole) of trimethylhydroquinone to about 0.9 to 1.1 mole (and preferably about 1.0 mole) of phytol or substituted phytol reacted in the presence of 0.1 to 1.5 mole (and preferably 0.35 to 0.75 mole) of combined acid condensation agent.
  • the amount of solvent present may vary, the minimal amount necessary being that amount suflicient for the reaction to take place.
  • the ratio of Lewis acid to strong acid should be from 1 to 3 moles Lewis acid to 1 mole strong acid. Generally, an inferior product is obtained if the amount of strong acid exceeds the amount of the Lewis acid.
  • a preferred set of molar ratios where the combined acid condensation agent consists of zinc chloride and sodium bisulfate, for example, would be 1.0 mole of trimethylhydroquinone, 1.0 mole of isophytol, and 0.575 mole of combined acid condensation agent, whose components are 0.3675 mole of zinc chloride and 0.2075 mole of sodium bisulfate.
  • the amount of combined acid condensation agent to be used may vary somewhat with the desired reaction time. Thus, more combined acid condensation agent may be used where a faster reaction is desirable, although the preferred maximum is 0.75 mole. Conversely, a smaller amount of combined acid condensation agent may be used where it is desired to slow down the reaction although the preferred minimum is 0.35 mole.
  • the general process of manufacture is for the trimethylhydroquinone to be charged into a reaction flask together with the combined acid condensing agent and the solvent. The mixture is then heated at 50 to 150 C. and isophytol is added slowly over a two to six hour period. The reaction mass is then further heated at 50-150" C. for from six to twenty-four hours. When the reaction is completed the mass may be purified by distillation if so desired.
  • One of the useful and unexpected results of using the combined acid condensing agent is that the d,l-
  • alpha-tocopherol produced is of about -95% purity
  • acetic anhydride may be added to produce d,l-alpha-tocopherol acetate.
  • EXAMPLE I 62.6 g. (0.4 mole of 98% purity) trimethylhydroquinone, 20.0 g. (0.147 mole) of zinc chloride, 10.0 g. (0.083 mole) sodium bisulfate and 240 m1. of benzene were charged into a one liter three-neck reaction flask. The first neck of the flask was equipped with a thermometer, the second with a mechanical agitator, and the third neck was connected to a Dean-Stark distillation receiver which was in turn connected to a reflux condenser. The reaction flask containing the above ingredients was heated to gentle reflux (7476 C.). 127.4 g.
  • Example II Example I was repeated with all ingredients in the same proportions except that in place of sodium bisulfate, 3.7 g. of concentrated sulfuric acid was used. This yielded 89.5% of 80% pure d,l-alpha-tocopheryl acetate.
  • Example III Example I was repeated with all ingredients in the same proportions except that in place of sodium bisulfate, 8.0 g. of para-toluene sulfonic acid was used. This yielded 91.0% of 86.3% pure d,l-alpha-tocopheryl acetate.
  • Example IV Example I was repeated with all ingredients in the same proportions except that in place of sodium bisulfate, 20 ml. of 37% of hydrochloric acid was used. This yielded 68% of 64% pure d,l-alpha-tocopheryl acetate.
  • EXAMPLE V 62.6 g. of trimethylhydroquinone, 20.0 g. of zinc chloride, 2.0 g. of sodium bisulfate, and 240 m1. of benzene were charged into a reaction flask and heated to reflux (85 C.). Heating was continued and 127.4 g. of isophytol were added over a two hour period. The reaction mass was further refluxed for 15 hours and then cooled, to produce d,l-alpha-tocopherol.
  • EXAMPLE VI 30.9 g. of trimethylhydroquinone, 10.0 g. of zinc chloride, 4.0 g. of p-toluene sulfonic acid, and 80 ml. of benzene were charged into a reaction flask and heated to reflux (80-85 C.). While maintaining the mixture at reflux temperature, 57.0 g. of isophytol were added over a two hour period. The reaction mass was further refluxed for fifteen hours and then cooled. The product thus produced was d,1-alpha-tocopherol.
  • a process for the manufacture of d,l-alpha-tocopherol comprising the condensation of trimethylhydroquinone with a phytol in the presence of an acid condensing agent and an inert solvent, the improvement comprising using a combined acid condensing agent that consists of a Lewis acid and at least one strong acid.
  • the strong acid is selected from at least one of a group consisting of sodium bisulfate, sulfuric acid and paratoluene sulfonic acid.

Abstract

D,1-ALPHA-TOCOPEROL IS PREPARED BY REACTING TRIMETHYLHYDROQUINONE (TMHQ) AND ISOPHYTOL IN THE PRESENCE OF A COMBINED ACID CONDENSATION AGENT WHICH COMPRISES A LEWIS ACID AND AT LEAST ONE STRONG ACID, WHICH COMBINED ACIDS ACT IN A SYNERGISTIC MANNER. A TYPICAL EXAMPLE OF A USEFUL LEWIS ACID IS ZINC CHLORIDE. TYPICAL EXAMPLES OF STRONG ACIDS ARE P-TOLUENE SULFONIC ACID AND SODIUM BISULFATE.

Description

United States Patent Oflice Patented Jan. 2, 1973 3,708,505 PROCESS FOR PREPARATION OF d,l-ALPHA TOCOPHEROL Sheldon B. Greenbaum, Livingston, N.J., and Walter Hacke, New York, and Herman Horn, Staten Island, N.Y., assignors to Diamond Shamrock Corporation, Cleveland, Ohio No Drawing. Filed Feb. 25, 1971, Ser. No. 119,048 Int. Cl. C07d 7/22 US. Cl. 260-3455 8 Claims ABSTRACT OF THE DISCLOSURE D,l-alpha-tocopherol is prepared by reacting trimethylhydroquinone (TMHQ) and isophytol in the presence of a combined acid condensation agent which comprises a Lewis acid and at least one strong acid, which combined acids act in a synergistic manner. A typical example of a usefulLewis acid is zinc chloride. Typical examples of strong acids are p-toluene sulfonic acid and sodium bisulfate.
BACKGROUND OF THE INVENTION (1) Field of the invention This invention relates to an improved process for manufacturing d,l-alpha-tocopherol.
(2) Description of the prior art The preparation of d,l-alpha-tocopl1erol by the condensation of trimethylhydroquinone and phytol or derivatives thereof in the presence of solvents and an acid condensing agent is well known in the art. The acid catalyst used in the prior art may be either a Lewis acid such as zinc chloride, boron tribromide, etc., or strong inorganic acids such as sulfuric acid, hydrochloric acid, etc., or strong organic acids such as p-toluene sulfonic acid.
SUMMARY OF THE INVENTION It has unexpectedly been discovered that by combining two individually known acid condensation agents in the known process for producing d,l-alpha-tocopherol, an improved product is obtained. The combined agents unexpectedly act in a synergistic manner which results in a product superior to that produced by using any one of them separately. In this improved process, trimethylhydroquinone and an inert organic solvent are charged into a reaction vessel together with a combination of at least one Lewis acid and at least one strong inorganic acid or strong organic acid and are heated to reflux. isophytol is then slowly added and when addition is completed the reaction mass is refluxed for a suflicient time to produce d,l-alpha-tocopherol. Optionally, acetic anhydride may be added to produce d,l-alpha-tocopheryl acetate. It is an advantage of the present process that the synthesis is essentially a one-step process and that a yield of high quality d,l-alpha-tocopherol is produced.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The phytol may be phytol, isophytol, phytadiene, phytyl chloride, phytyl bromide, phytyl acetate, phytyl methyl ether, phytol derivatives, substituted phytol, and the like. The preferred phytol is isophytol.
v Inert organic solvents which may be employed in the present invention are those solvents boiling below the boiling points of the reactants and the desired product. Suitable inert solvents include the aliphatic hydrocarbon solvents of to 12 carbon atoms, or more, as for example, n-heptane; carboxylic acids having 2 to 6 carbon atoms such as acetic acid, propionic acid, butanoic acid, and
hexanoic acid; aromatic solvents such as xylene, benzene, and toluene; ethers such as isopropyl ether, dioxane, tetrahydrofuran; and the like.
The acid condensation catalyst of this invention must consist of a combination of two acids, one of which must be a Lewis acid and the other a strong acid which may be organic or inorganic.
Suitable Lewis acids include boron trifluoride, boron tribromide, aluminum chloride, aluminum bromide, zinc chloride, boron trifluorodiphosphoric acid complex, and the like. The preferred Lewis acid is zinc chloride.
Suitable strong acids include sulfuric acid, hydrochloric acid, nitric acid, para-toluene sulfonic acid, sodium bisulfate, mixtures thereof, and the like. Preferred strong acids are sulfuric acid, para-toluene sulfonic acid and sodium bisulfate. An especially preferred strong acid is sodium bisulfate.
The ratio of ingredients is from about 0.9 to 1.1 mole (and preferably about 1.0 mole) of trimethylhydroquinone to about 0.9 to 1.1 mole (and preferably about 1.0 mole) of phytol or substituted phytol reacted in the presence of 0.1 to 1.5 mole (and preferably 0.35 to 0.75 mole) of combined acid condensation agent. The amount of solvent present may vary, the minimal amount necessary being that amount suflicient for the reaction to take place. The ratio of Lewis acid to strong acid should be from 1 to 3 moles Lewis acid to 1 mole strong acid. Generally, an inferior product is obtained if the amount of strong acid exceeds the amount of the Lewis acid. A preferred set of molar ratios where the combined acid condensation agent consists of zinc chloride and sodium bisulfate, for example, would be 1.0 mole of trimethylhydroquinone, 1.0 mole of isophytol, and 0.575 mole of combined acid condensation agent, whose components are 0.3675 mole of zinc chloride and 0.2075 mole of sodium bisulfate. The amount of combined acid condensation agent to be used may vary somewhat with the desired reaction time. Thus, more combined acid condensation agent may be used where a faster reaction is desirable, although the preferred maximum is 0.75 mole. Conversely, a smaller amount of combined acid condensation agent may be used where it is desired to slow down the reaction although the preferred minimum is 0.35 mole.
The general process of manufacture is for the trimethylhydroquinone to be charged into a reaction flask together with the combined acid condensing agent and the solvent. The mixture is then heated at 50 to 150 C. and isophytol is added slowly over a two to six hour period. The reaction mass is then further heated at 50-150" C. for from six to twenty-four hours. When the reaction is completed the mass may be purified by distillation if so desired. One of the useful and unexpected results of using the combined acid condensing agent is that the d,l-
alpha-tocopherol produced is of about -95% purity,
which meets feed grade standards. Purification is therefore only required if the product is to meet National Formulary standards. Alternately, acetic anhydride may be added to produce d,l-alpha-tocopherol acetate.
For a fuller understanding of the nature and objects of this invention, reference may be made to the following examples which are given merely to illustrate the invention and are not to be construed in a limiting sense. All weights, proportions, and percentages, are on a weight basis unless otherwise indicated. All temperatures are C. unless otherwise indicated.
EXAMPLE I 62.6 g. (0.4 mole of 98% purity) trimethylhydroquinone, 20.0 g. (0.147 mole) of zinc chloride, 10.0 g. (0.083 mole) sodium bisulfate and 240 m1. of benzene were charged into a one liter three-neck reaction flask. The first neck of the flask was equipped with a thermometer, the second with a mechanical agitator, and the third neck was connected to a Dean-Stark distillation receiver which was in turn connected to a reflux condenser. The reaction flask containing the above ingredients was heated to gentle reflux (7476 C.). 127.4 g. (0.4 mole of 96.1% purity) isophytol were slowly added over a 2.5 hour period. Thereafter, the reaction mass was heated at reflux (8486 C.) for 16 hours and cooled to room temperature. 85.0 g. (0.83 mole) of acetic anhydride was then added and the reaction mass was again brought to reflux and maintained at that temperature for 6 hours. After cooling the reaction mass was washed with 200 ml. of 10% brine and the washing was then repeated two more times with 160 ml. of 10% brine. The organic layer was then dried over Na SO and the solvent stripped off at 6070 C. The residue weighed 197.8 g. and was 89.5% pure d,l-alpha-tocopheryl acetate as determined by gas chromatography. This yield corresponded to 93.6% of the theoretical maximum recovery.
EXAMPLE II Example I was repeated with all ingredients in the same proportions except that in place of sodium bisulfate, 3.7 g. of concentrated sulfuric acid was used. This yielded 89.5% of 80% pure d,l-alpha-tocopheryl acetate.
EXAMPLE III Example I was repeated with all ingredients in the same proportions except that in place of sodium bisulfate, 8.0 g. of para-toluene sulfonic acid was used. This yielded 91.0% of 86.3% pure d,l-alpha-tocopheryl acetate.
EXAMPLE IV Example I was repeated with all ingredients in the same proportions except that in place of sodium bisulfate, 20 ml. of 37% of hydrochloric acid was used. This yielded 68% of 64% pure d,l-alpha-tocopheryl acetate.
TABLE I Summary of the Results of Examples I-lV The following table illustrates the comparative merits of various strong acids combined with a Lewis acid (zinc chloride) for achieving the purposes of this invention.
Percent Percent Strong acid yield purity Sodium bisulfate 93. 6 89. Parartoluene sulfonic acid-.. 91.0 86. 3 sulphuric acid 89. 5 80.0 Hydrochloric acid 68.0 64. 0
minimizes the waste of raw materials which occurs in many of the processes of the prior art.
EXAMPLE V 62.6 g. of trimethylhydroquinone, 20.0 g. of zinc chloride, 2.0 g. of sodium bisulfate, and 240 m1. of benzene were charged into a reaction flask and heated to reflux (85 C.). Heating was continued and 127.4 g. of isophytol were added over a two hour period. The reaction mass was further refluxed for 15 hours and then cooled, to produce d,l-alpha-tocopherol.
EXAMPLE VI 30.9 g. of trimethylhydroquinone, 10.0 g. of zinc chloride, 4.0 g. of p-toluene sulfonic acid, and 80 ml. of benzene were charged into a reaction flask and heated to reflux (80-85 C.). While maintaining the mixture at reflux temperature, 57.0 g. of isophytol were added over a two hour period. The reaction mass was further refluxed for fifteen hours and then cooled. The product thus produced was d,1-alpha-tocopherol.
We claim:
1. In a process for the manufacture of d,l-alpha-tocopherol comprising the condensation of trimethylhydroquinone with a phytol in the presence of an acid condensing agent and an inert solvent, the improvement comprising using a combined acid condensing agent that consists of a Lewis acid and at least one strong acid.
2. The improved process according to claim 1 in which the Lewis acid is zinc chloride.
3. The improved process according to claim 1 in which the strong acid is selected from at least one of a group consisting of sodium bisulfate, sulfuric acid and paratoluene sulfonic acid.
4. The improved process according to claim 1 in which the strong acid is sodium bisulfate.
5. The improved process according to claim 1 in which the Lewis acid is zinc chloride and the strong acid is sodium bisulfate.
6. The improved process according to claim 1 in which about 1.0 mole of trimethylhydroquinone is condensed with about 1.0 mole of isophytol in the presence of from about .35 to about .75 mole of combined acid condensing agent.
7. The improved process according to claim 6 in which the ratio of the combined acid condensing agent is from about 1 to about 3 mole Lewis acid to about 1 mole strong acid.
8. The improved process according to claim 1 in which acetic anhydride is reacted with the d,l-alpha-tocopherol to produce d,l-alpha-tocopheryl acetate.
References Cited UNITED STATES PATENTS JOHN M. FORD, Primary Examiner
US00119048A 1971-02-25 1971-02-25 Process for preparation of d,l-alpha tocopherol Expired - Lifetime US3708505A (en)

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Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4055575A (en) * 1975-03-20 1977-10-25 Scm Corporation Synthesis of dehydrophytol and vitamin E
US4191692A (en) * 1976-02-20 1980-03-04 Basf Aktiengesellschaft Manufacture of tocopherol
US5468883A (en) * 1992-03-17 1995-11-21 Basf Aktiengesellschaft Preparation of vitamin E
EP0782993A1 (en) * 1996-01-05 1997-07-09 F. Hoffmann-La Roche Ag Process for the preparation of d,l-alpha-tocopherol in the presence of a perfluoroalkenesulfonic acid catalyst
US5744617A (en) * 1995-05-10 1998-04-28 Rhone-Poulenc Nutrition Animale Process for the preparation of substituted phenols
EP0850937A1 (en) * 1996-12-23 1998-07-01 Basf Aktiengesellschaft Process for the preparation of alpha-tocopherol or alpha-tocopheryl acetate by reacting trimethylhydroquinone and phytol or isophytol and recycling the zinc halogenide condensation catalyst
EP0949255A1 (en) * 1998-04-06 1999-10-13 F. Hoffmann-La Roche Ag Process for manufacturing d, 1-alpha-tocopherol in a carbonate solvent and in the presence of a sulphur-containing acid catalyst
US20030153772A1 (en) * 1998-09-18 2003-08-14 Aventis Animal Nutrition, S.A., Process for the preparation of vitamin E
EP0694541B2 (en) † 1994-07-27 2004-03-03 Eisai Co., Ltd. Process for the preparation of alpha-tocopherol
WO2004046126A1 (en) * 2002-11-21 2004-06-03 Dsm Ip Assets B.V. Manufacture of tocopheryl acetate
US6784303B2 (en) 2000-11-22 2004-08-31 Basf Aktiengesellschaft Method for continuously acylating chromanol ester derivatives
US20050277777A1 (en) * 2004-06-11 2005-12-15 Werner Bonrath Process for the manufacture of chroman derivatives, especially alpha-tocopherol and alkanoates thereof
CN106565659A (en) * 2016-11-01 2017-04-19 万华化学集团股份有限公司 Method of preparing vitamin E acetate
CN108409704A (en) * 2018-01-24 2018-08-17 上海优合生物科技有限公司 A kind of preparation method of high-purity tocopherol succinate salt

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2606830C3 (en) * 1976-02-20 1981-08-27 Basf Ag, 6700 Ludwigshafen Process for the production of tocopherol
JPS6019309B2 (en) * 1976-09-29 1985-05-15 日清製粉株式会社 Production method of high purity dl-α-tocopherol
DE3203487A1 (en) * 1982-02-03 1983-08-11 Basf Ag, 6700 Ludwigshafen METHOD FOR PRODUCING TOCOPHERYL ACETATE OR TOCOPHERYL PROPIONATE
DE60333493D1 (en) * 2003-01-13 2010-09-02 Dsm Ip Assets Bv PROCESS FOR PREPARING ALPHA TOCOPHEROL ACETATE

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2411969A (en) * 1938-03-31 1946-12-03 Hoffmann La Roche Process for the preparation of synthetic dl-tocopherols
US2411968A (en) * 1938-03-31 1946-12-03 Hoffmann La Roche Process for the preparation of synthetic dl-tocopherols

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4055575A (en) * 1975-03-20 1977-10-25 Scm Corporation Synthesis of dehydrophytol and vitamin E
US4191692A (en) * 1976-02-20 1980-03-04 Basf Aktiengesellschaft Manufacture of tocopherol
US5468883A (en) * 1992-03-17 1995-11-21 Basf Aktiengesellschaft Preparation of vitamin E
EP0694541B2 (en) † 1994-07-27 2004-03-03 Eisai Co., Ltd. Process for the preparation of alpha-tocopherol
US5744617A (en) * 1995-05-10 1998-04-28 Rhone-Poulenc Nutrition Animale Process for the preparation of substituted phenols
EP0782993A1 (en) * 1996-01-05 1997-07-09 F. Hoffmann-La Roche Ag Process for the preparation of d,l-alpha-tocopherol in the presence of a perfluoroalkenesulfonic acid catalyst
US5900494A (en) * 1996-01-05 1999-05-04 Roche Vitamins Inc. Method of making d,l-α-tocopherol
EP0850937A1 (en) * 1996-12-23 1998-07-01 Basf Aktiengesellschaft Process for the preparation of alpha-tocopherol or alpha-tocopheryl acetate by reacting trimethylhydroquinone and phytol or isophytol and recycling the zinc halogenide condensation catalyst
US6005122A (en) * 1996-12-23 1999-12-21 Basf Aktiengesellschaft Preparation of α-tocopherol or α-tocopheryl acetate by reacting trimethylhydroquinone and phytol or isophytol, with recycling of the zinc halide condensation catalyst
EP0949255A1 (en) * 1998-04-06 1999-10-13 F. Hoffmann-La Roche Ag Process for manufacturing d, 1-alpha-tocopherol in a carbonate solvent and in the presence of a sulphur-containing acid catalyst
US6066745A (en) * 1998-04-06 2000-05-23 Roche Vitamins Inc. Process for the synthesis of vitamin E
US20030153772A1 (en) * 1998-09-18 2003-08-14 Aventis Animal Nutrition, S.A., Process for the preparation of vitamin E
US6790967B2 (en) 1998-09-18 2004-09-14 Adisseo France S.A.S. Process for the preparation of vitamin E
US6784303B2 (en) 2000-11-22 2004-08-31 Basf Aktiengesellschaft Method for continuously acylating chromanol ester derivatives
WO2004046126A1 (en) * 2002-11-21 2004-06-03 Dsm Ip Assets B.V. Manufacture of tocopheryl acetate
US20060094886A1 (en) * 2002-11-21 2006-05-04 Werner Bonrath Manufacture of tocopheryl acetate
US7169943B2 (en) 2002-11-21 2007-01-30 Dsm Ip Assets B.V. Manufacture of tocopheryl acetate
US20070112206A1 (en) * 2002-11-21 2007-05-17 Werner Bonrath Manufacture of tocopheryl acetate
US20050277777A1 (en) * 2004-06-11 2005-12-15 Werner Bonrath Process for the manufacture of chroman derivatives, especially alpha-tocopherol and alkanoates thereof
US20090176998A1 (en) * 2004-06-11 2009-07-09 Werner Bonrath Process for the manufacture of chroman derivatives, especially alpha-tocopherol and alka-noates thereof
US8431727B2 (en) 2004-06-11 2013-04-30 Dsm Assets B.V. Process for the manufacture of chroman derivatives, especially α-tocopherol and alka-noates thereof
CN106565659A (en) * 2016-11-01 2017-04-19 万华化学集团股份有限公司 Method of preparing vitamin E acetate
CN108409704A (en) * 2018-01-24 2018-08-17 上海优合生物科技有限公司 A kind of preparation method of high-purity tocopherol succinate salt

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IT990452B (en) 1975-06-20
FR2126214A1 (en) 1972-10-06
GB1371701A (en) 1974-10-23
DE2208795B2 (en) 1978-03-09
FR2126214B1 (en) 1977-07-15
IL38718A0 (en) 1972-04-27
JPS5341154B1 (en) 1978-10-31
CA968805A (en) 1975-06-03
DE2208795C3 (en) 1978-11-02
DE2208795A1 (en) 1972-08-31

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