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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238943생성일: 2026년 10월 25일

Benzyl 2,2,2-trichloroacetimidate → (3S)-3-(benzyloxy)butanoic acid ethyl ester

https://huagongshe.com/reaction/238943

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl 2,2,2-trichloroacetimidateHCID 144968—
반응물Butanoic acid, 3-hydroxy-, ethyl ester, (3S)-HCID 6950306—
촉매Trifluoromethanesulfonic acidHCID 62406—
용매DichloromethaneHCID 6344—
생성물(3S)-3-(benzyloxy)butanoic acid ethyl esterHCID 14201835200.7%

반응 단계

Under a nitrogen atmosphere, to a solution of (S)-(+)-3-hydroxybutyric acid ethyl ester (100 g, 0.76 mol) in methylene chloride (1.0 L), benzyl 2,2,2-trichloroacetoimidate (381 g, 1.5 mol) and trifluoromethanesulfonic acid (6.7 mL, 76 mmol) were gradually added, and the mixture was stirred at room temperature overnight. The precipitated solid was filtered, and after the mother liquid was successively washed with a saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, it was dried with sodium sulfate and the solvent was distilled off under reduced pressure. Hexane was added to the residue, and after the solid was filtered again, the solvent of the mother liquid was distilled off under reduced pressure to give (3S)-3-(benzyloxy)butanoic acid ethyl ester (339 g) as a mixture. The present compound was used for the subsequent reaction without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642640B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-8f6474ba20e846e49214da9fa1a069b8
출처 메모uspto-grants-2014_02