GB816224A - Preparation of vitamin a esters - Google Patents

Preparation of vitamin a esters

Info

Publication number
GB816224A
GB816224A GB2117/56A GB211756A GB816224A GB 816224 A GB816224 A GB 816224A GB 2117/56 A GB2117/56 A GB 2117/56A GB 211756 A GB211756 A GB 211756A GB 816224 A GB816224 A GB 816224A
Authority
GB
United Kingdom
Prior art keywords
palmitate
vitamin
methyl
fatty acid
higher fatty
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB2117/56A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Publication of GB816224A publication Critical patent/GB816224A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Higher fatty acid esters of Vitamin A are obtained by esterifying Vitamin A with a higher fatty acid ester of a lower alkyl monohydric alcohol in the presence of a basic alcoholysis catalyst. As higher fatty acid esters of lower alkyl monohydric alcohols there may be used methyl palmitate, ethyl palmitate, butyl stearate, methyl oleate, propyl linoleate, methyl myristate and methyl laurate. As basic alcoholysis catalysts there may be used sodium methoxide, potassium ethoxide, lithium isopropoxide, calcium methoxide, barium isopropoxide, sodium hydride, potassium amide, sodium palmitate, lithium palmitate and barium hydroxide. The temperature of reaction is varied according to the catalyst employed. Sodium methoxide may be employed at about 0.2-0.5 per cent by weight of the reaction composition. The reaction is effected in an inert solvent, e.g. xylene, benzene, petroleum ether, and diethyl ether. An example describes the preparation of Vitamin A palmitate.
GB2117/56A 1955-10-31 1956-01-23 Preparation of vitamin a esters Expired GB816224A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US816224XA 1955-10-31 1955-10-31

Publications (1)

Publication Number Publication Date
GB816224A true GB816224A (en) 1959-07-08

Family

ID=22165303

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2117/56A Expired GB816224A (en) 1955-10-31 1956-01-23 Preparation of vitamin a esters

Country Status (1)

Country Link
GB (1) GB816224A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108623507A (en) * 2017-03-15 2018-10-09 四川海思科制药有限公司 The preparation method of Retinol Palmitate
CN113957114A (en) * 2021-11-22 2022-01-21 万华化学集团股份有限公司 Method for synthesizing vitamin A palmitate by enzyme method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108623507A (en) * 2017-03-15 2018-10-09 四川海思科制药有限公司 The preparation method of Retinol Palmitate
CN113957114A (en) * 2021-11-22 2022-01-21 万华化学集团股份有限公司 Method for synthesizing vitamin A palmitate by enzyme method
CN113957114B (en) * 2021-11-22 2023-05-26 万华化学集团股份有限公司 Method for synthesizing vitamin A palmitate by enzyme method

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