Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 732276생성일: 2026년 10월 23일
Tert-butyl 3-(benzyloxycarbonylamino)-4-hydroxy-pyrrolidine-1-carboxylate → 1-Methyl-4-(methylamino)pyrrolidin-3-OL
https://huagongshe.com/ko/reaction/732276
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tert-butyl 3-(benzyloxycarbonylamino)-4-hydroxy-pyrrolidine-1-carboxylate | HCID 20691380 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Methyl-4-(methylamino)pyrrolidin-3-OL | HCID 68465076 | 18% |
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 Na2SO4.10H2O, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07585975B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-517b1a151371432f8a873afce9e63243 |
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| 출처 메모 | uspto-grants-2009_09 |
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