JPS554328A - Preparation of phytol fatty acid ester - Google Patents

Preparation of phytol fatty acid ester

Info

Publication number
JPS554328A
JPS554328A JP7662778A JP7662778A JPS554328A JP S554328 A JPS554328 A JP S554328A JP 7662778 A JP7662778 A JP 7662778A JP 7662778 A JP7662778 A JP 7662778A JP S554328 A JPS554328 A JP S554328A
Authority
JP
Japan
Prior art keywords
fatty acid
dmf
phytol
objective compound
compound
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.)
Pending
Application number
JP7662778A
Other languages
Japanese (ja)
Inventor
Takayuki Shibamoto
Takuya Akiyama
Kunio Tanaka
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.)
OGAWA KORYO KK
Original Assignee
OGAWA KORYO KK
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 OGAWA KORYO KK filed Critical OGAWA KORYO KK
Priority to JP7662778A priority Critical patent/JPS554328A/en
Publication of JPS554328A publication Critical patent/JPS554328A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE: To prepare the title compound useful as a component of essential oil of jasmine, easily, in high purity, by reacting a fatty acid with a thionyl halide in DMF, and then reacting the reaction product with phytol.
CONSTITUTION: A fatty acid (pref. 10-20C saturated or unsaturated fatty acid, e.g. palmitic acid, stearic acid, etc.) is dissolved in DMF, and made to react with a thionyl halide. Without separating the reaction mixture, it is further reacted with phytol to obtain the objective compound. Since the objective compound has low solubility to DMF, the reaction mixture can be easily separated into two phases, i.e. a DMF layer containing unreacted fatty acid, etc., and a layer containing the objective compound.
EFFECT: Since the difficult separation process of the unreacted fatty acid from the objective compound is not necessary, the process enables the production of the compound in large quantity.
COPYRIGHT: (C)1980,JPO&Japio
JP7662778A 1978-06-22 1978-06-22 Preparation of phytol fatty acid ester Pending JPS554328A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7662778A JPS554328A (en) 1978-06-22 1978-06-22 Preparation of phytol fatty acid ester

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7662778A JPS554328A (en) 1978-06-22 1978-06-22 Preparation of phytol fatty acid ester

Publications (1)

Publication Number Publication Date
JPS554328A true JPS554328A (en) 1980-01-12

Family

ID=13610593

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7662778A Pending JPS554328A (en) 1978-06-22 1978-06-22 Preparation of phytol fatty acid ester

Country Status (1)

Country Link
JP (1) JPS554328A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5170727A (en) * 1991-03-29 1992-12-15 Union Carbide Chemicals & Plastics Technology Corporation Supercritical fluids as diluents in combustion of liquid fuels and waste materials

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5170727A (en) * 1991-03-29 1992-12-15 Union Carbide Chemicals & Plastics Technology Corporation Supercritical fluids as diluents in combustion of liquid fuels and waste materials

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