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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5621생성일: 2026년 10월 23일

Trifluoromethanesulfonic acid → Methyl (3R)-3-(benzyloxy)tetradecanoate

https://huagongshe.com/ko/reaction/5621

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물Benzyl 2,2,2-trichloroacetimidateHCID 144968—
반응물3R-hydroxymyristic acid methyl esterHCID 9834945—
용매CyclohexaneHCID 8078—
생성물Methyl (3R)-3-(benzyloxy)tetradecanoateHCID 13817922112.8%

반응 단계

A suspension of 206.7 g of methyl (R)-3-hydroxytetradecanoate in 1000 ml of cyclohexane was treated under nitrogen and while stirring with 214.2 g of benzyl trichloroacetimidate and dissolved at 20°. 10 ml of trifluoromethanesulphonic acid were added dropwise while cooling in an ice/water bath in such a manner that the temperature remains between 20°-23°. The resulting suspension was stirred at 25°-30°. The precipitate was filtered off, the filter cake was washed with cyclohexane, the filtrates were extracted with sat. NaHCO3 solution, water and sat. NaCl solution. The organic phase was dried over magnesium sulphate, filtered, the filter cake was washed with cyclohexane and the filtrates were evaporated. 314.5 g of methyl (R)-3-(benzyloxy)-tetradecanoate were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245056
출처 데이터셋uspto-grants-1993_09
ORD IDord-7aa6ea05ad5f4e639b91d1a44ecf298b
출처 메모uspto-grants-1993_09