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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

반응식

참여 물질

역할이름HCID투입량
반응물Methyl AcrylateHCID 7294—
반응물QuinuclidineHCID 7527—
반응물HCID 89863093HCID 89863093—
용매MethanolHCID 887—
생성물methyl 4-(tert-butoxycarbonyl((S)-1-methoxybut-3-en-2-yl)amino)-3-hydroxy-2-methylenebutanoateHCID 8985137665%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09309245B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-e080e644243f4d5097cb3905e31e5222
출처 메모uspto-grants-2016_04