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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1783606생성일: 2026년 10월 25일

Tert-butyl 3-(benzyloxycarbonylamino)-4-hydroxy-pyrrolidine-1-carboxylate → 1-Methyl-4-(methylamino)pyrrolidin-3-OL

https://huagongshe.com/reaction/1783606

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl 3-(benzyloxycarbonylamino)-4-hydroxy-pyrrolidine-1-carboxylateHCID 20691380—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
생성물1-Methyl-4-(methylamino)pyrrolidin-3-OLHCID 6846507618%

반응 조건

온도0 °C

반응 단계

LAH (1.40 g, 35.0 mmol) is slowly added to a stirred solution of 3-benzyloxycarbonylamino-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester in THF (15 ml) at room temperature. The reaction mixture is heated to reflux under N2 for 2 hours and then cooled to 0° C. The reaction mixture is quenched by the slow addition of Na2SO4.10 H2O, warmed to room temperature, diluted with ethyl acetate and filtered through Celite. The filtrate is concentrated and purified on a silica gel column (10:1:0.5 methylene chloride, MeOH, 30% NH4OH solution) to yield 0.21 g (18% for two steps) 1-methyl-4-methylamino-pyrrolidin-3-ol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07501427B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-010bd08ef7d143ec9d0b4a56a6da7160
출처 메모uspto-grants-2009_03