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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56401생성일: 2026년 10월 23일

Chlorotrimethylsilane → (R)-3-((2S,3S,E)-2-allyl-3-hydroxy-5-phenylpent-4-enoyl)-4-benzyloxazolidin-2-one

https://huagongshe.com/ko/reaction/56401

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물TriethylamineHCID 8471—
반응물CinnamaldehydeHCID 637511—
반응물Magnesium ChlorideHCID 5360315—
반응물SodiumHCID 5360545—
반응물(R)-4-Benzyl-3-pent-4-enoyloxazolidin-2-oneHCID 10858190—
용매Ethyl AcetateHCID 8857—
생성물(R)-3-((2S,3S,E)-2-allyl-3-hydroxy-5-phenylpent-4-enoyl)-4-benzyloxazolidin-2-oneHCID 6711356180%

반응 단계

A mixture of (R)-4-benzyl-3-pent-4-enoyloxazolidin-2-one (50 g, 193 mmol), magnesium chloride (18.3 g, 193 mmol), sodium hexafluorostibate(V) (14.9 g, 58 mmol), triethylamine (80 mL, 579 mmol), (trans)-cinnamaldehyde (30.6 g, 232 mmol) and chlorotrimethylsilane (37.2 mL, 290 mmol) in ethyl acetate (500 mL) was stirred at room temperature for 17 hours. The mixture was diluted with ethyl acetate and filtered to remove solids. The filtrate was concentrated to small volume, and then diluted with methanol (500 mL) and a small amount of ethyl acetate. After treatment with trifluoroacetic acid (3 mL), the resulting solution was stirred at room temperature for 1 h, and then concentrated to dryness under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:petroleum ether=1:10) to afford the title compound (60 g, 80%) as a yellow semi-solid. MS (ES+) C24H25NO4 requires: 391, found: 374 [M+H−H2O]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434700B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-4c695542b1dc42d2a9c99d233bd7e03b
출처 메모uspto-grants-2016_09