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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2390572생성일: 2026년 10월 25일

Isopropanol → (S)-3-((R)-1-Hydroxy-2-isopropoxyethyl)pyrrolidine-1-carboxylic Acid t-Butyl Ester

https://huagongshe.com/reaction/2390572

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물(S)-(R)-3-Oxiranylpyrrolidine-1-carboxylic acid t-butyl esterHCID 86650334—
생성물(S)-3-((R)-1-Hydroxy-2-isopropoxyethyl)pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 66859524—

반응 조건

온도0 °C

반응 단계

Isopropyl alcohol (215 μL, 2.8 mmol) was dissolved in THF (428 μL), and the mixture was cooled at 0° C. NaH (33.8 mg, 1.4 mmol) was added in 4 portions, and the mixture stirred for 10 minutes at room temperature. (S)—(R)-3-Oxiranylpyrrolidine-1-carboxylic acid t-butyl ester (200 mg, 938 μmol) was added. The resulting solution was placed in a microwave reactor for 10 minutes at 100° C., then cooled to room temperature. The mixture was extracted with Hexanes (10 mL) and washed with 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 give the title compound as a clear oil (162 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08273786B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-caa2431f3cbc4b08b360d103635842e9
출처 메모uspto-grants-2012_09