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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Cinnamaldehyde | HCID 637511 | — |
| 반응물 | Magnesium Chloride | HCID 5360315 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | (R)-4-Benzyl-3-pent-4-enoyloxazolidin-2-one | HCID 10858190 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (R)-3-((2S,3S,E)-2-allyl-3-hydroxy-5-phenylpent-4-enoyl)-4-benzyloxazolidin-2-one | HCID 67113561 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434700B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-4c695542b1dc42d2a9c99d233bd7e03b |
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| 출처 메모 | uspto-grants-2016_09 |
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