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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 533389생성일: 2026년 10월 25일

Water → (S)-3-((R)-2-Ethylsulfanyl-1-hydroxyethyl)pyrrolidine-1-carboxylic Acid t-Butyl Ester

https://huagongshe.com/reaction/533389

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물EthanethiolHCID 6343—
반응물Sodium hydrideHCID 24758—
반응물(S)-(R)-3-Oxiranylpyrrolidine-1-carboxylic acid t-butyl esterHCID 86650334—
용매TetrahydrofuranHCID 8028—
생성물(S)-3-((R)-2-Ethylsulfanyl-1-hydroxyethyl)pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 6685994181.7%

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온도0 °C

반응 단계

Ethanethiol (312 μL, 4.2 mmol) was dissolved in THF (1.0 mL), and the mixture was cooled to 0° C. NaH (50.6 mg, 2.1 mmol) was slowly added in four portions and the mixture was stirred at room temperature for 10 minutes. (S)—(R)-3-Oxiranylpyrrolidine-1-carboxylic acid t-butyl ester (300 mg, 1.4 mmol) was dissolved in THF (0.4 mL) and added to the mixture. The resulting solution was placed in a microwave reactor for 30 minutes at 100° C., then cooled to room temperature. Hexanes (3×10 mL) was added, followed by water (10 mL). The organic layer was collected, dried over Na2SO4, filtered, and concentrated. The crude product was purified by column chromatography (0-100% EtOAc in hexanes) to yield the title compound as a clear oil (315 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853255B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-efce8e1375d2461fb07ade2df4868605
출처 메모uspto-grants-2014_10