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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 376416생성일: 2026년 10월 25일

Oleyl p-toluenesulfonate → 1,3-O-dioleyl-2-O-tetrahydrofuranylglycerol

https://huagongshe.com/reaction/376416

반응식

참여 물질

역할이름HCID투입량
반응물Oleyl p-toluenesulfonateHCID 11258749—
반응물2-O-tetrahydrofuranylglycerolHCID 19361256—
반응물HCID 178418922HCID 178418922—
용매O-XyleneHCID 7237—
생성물1,3-O-dioleyl-2-O-tetrahydrofuranylglycerolHCID 7025637418%

반응 단계

In 30 ml of xylene was dissolved 854 mg (5.3 mmol) of 2-O-tetrahydrofuranylglycerol. To this was added 1.78 g (15.9 mmol) of t-butoxypotassium under argon gas and the mixture was stirred for 5 minutes. Then, 10 ml of a solution of 6.71 g (15.9 mmol) oleyl p-toluenesulfonate in xylene was added dropwise and the mixture was stirred under reduced pressure (20-30 mmHg) at ambient temperature for 30 minutes and further at 50° C. for 1 hour. This reaction mixture was poured in ice-water and extracted with ether, and the extract was washed with water, dried, and concentrated. The residue was purified by column chromatography (silica gel/chloroform) to provide 628 mg (18%) of 1,3-O-dioleyl-2-O-tetrahydrofuranylglycerol as yellow oil. (5) In 30 ml of tetrahydrofuran was dissolved 628 mg (0.95 mmol) of 1,3-O-dioleyl-2-O-tetrahydrofuranylglycerol followed by addition of 5 ml of diluted (10%) hydrochloric acid, and the mixture was stirred overnight. The reaction mixture was then diluted with water, neutralized with saturated aqueous sodium hydrogen carbonate solution, and extracted with ether. The extract was dried and concentrated and the residue was subjected to column chromatography (silica gel/n-hexane-ethyl acetate) to provide 321 mg (57%) of the title compound as colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06020317
출처 데이터셋uspto-grants-2000_02
ORD IDord-462aa6735f5049069925dc7e93bf77c6
출처 메모uspto-grants-2000_02