Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 627262생성일: 2026년 10월 24일
Methyl Acrylate → methyl 4-(tert-butoxycarbonyl((S)-1-methoxybut-3-en-2-yl)amino)-3-hydroxy-2-methylenebutanoate
https://huagongshe.com/ko/reaction/627262
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl Acrylate | HCID 7294 | — |
| 반응물 | Quinuclidine | HCID 7527 | — |
| 반응물 | HCID 89863093 | HCID 89863093 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | methyl 4-(tert-butoxycarbonyl((S)-1-methoxybut-3-en-2-yl)amino)-3-hydroxy-2-methylenebutanoate | HCID 89851376 | 65% |
반응 단계
To a solution of (S)-tert-butyl 1-methoxybut-3-en-2-yl(2-oxoethyl)carbamate (Intermediate 252, 1.475 g, 6.06 mmol) and methyl acrylate (0.82 ml, 9.09 mmol) in MeOH (0.2 ml) under nitrogen at room temperature was added quinuclidine (0.337 g, 3.03 mmol). The reaction mixture was stirred at that temperature overnight. Another 100 mg of quinuclidine was added and the reaction was stirred for another 24 hours. The reaction mixture was then partitioned between water and ethyl acetate. The layers were separated and the organics were washed with water and brine, then dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography (0%-30% ethyl acetate/hexanes) afforded the title compound as a clear oil (1.28 g, 65%). The product is a mixture of two diastereomers.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09309245B2 |
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| 출처 데이터셋 | uspto-grants-2016_04 |
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| ORD ID | ord-e080e644243f4d5097cb3905e31e5222 |
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| 출처 메모 | uspto-grants-2016_04 |
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