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HRID 6256생성일: 2026년 10월 23일

Acetic Acid → (S)-1-Benzyloxy-3-(t-butyldiphenylsilyloxy)propan-2-ol

https://huagongshe.com/ko/reaction/6256

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물ImidazoleHCID 795—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
반응물(R)-3-(benzyloxy)propane-1,2-diolHCID 2724795—
용매TetrahydrofuranHCID 8028—
생성물(S)-1-Benzyloxy-3-(t-butyldiphenylsilyloxy)propan-2-olHCID 1098269890%

반응 단계

To a solution of (R)-3-benzyloxypropane-1,2-diol (prepared from (S)-4-benzylymethyl-2,2-dimethyl-1,3-dioxolane (commercially available from FLUKA) by acid hydrolysis using 80% aqueous acetic acid), (8.3 g, 47.2 mmol) in dry THF (70 ml) was added imidazole (6.42 g, 94.4 mmol). After 2 minutes, t-butyldiphenylsilyl chloride (12.28 ml, 47.2 mmol) was added. A white precipitate formed immediately. After 2 hours, the reaction mixture was filtered and the filtrate evaporated. The residue was partitioned between ethyl acetate and water, the organic layer separated, washed with saturated brine, dried (MgSO4), filtered and evaporated to give a colourless oil. Chromatography of the oil on silica gel (dichloromethane as eluant) afforded the title compound as a colourless oil (17.72 g, 90%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05247085
출처 데이터셋uspto-grants-1993_09
ORD IDord-cf9e57ba9a5d488b84ad34a0e5f55896
출처 메모uspto-grants-1993_09