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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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[(3R,4R)-4-azidotetrahydrofuran-3-yl]oxy-tert-butyl-dimethyl-silane → (3R,4R)-4-(tert-Butyl(dimethyl)silyl)oxytetrahydrofuran-3-amine

HRID 245063
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인쇄 미리보기

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HRID 245063 반응식
[N:1]([C@@H:4]1[CH2:8][O:7][CH2:6][C@@H:5]1[O:9][Si:10]([C:13]([CH3:16])([CH3:15])[CH3:14])([CH3:12])[CH3:11])=[N+]=[N-]>[Pd].C(O)C>[Si:10]([O:9][C@H:5]1[CH2:6][O:7][CH2:8][C@H:4]1[NH2:1])([C:13]([CH3:16])([CH3:15])[CH3:14])([CH3:12])[CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86693775[(3R,4R)-4-azidotetrahydrofuran-3-yl]oxy-tert-butyl-dimethyl-silane

생성물 1

HCID 71151039(3R,4R)-4-(tert-Butyl(dimethyl)silyl)oxytetrahydrofuran-3-amine수율 88.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of [(3R,4R)-4-azidotetrahydrofuran-3-yl]oxy-tert-butyl-dimethyl-silane (1.27 g, 5.22 mmol) and 10% palladium on carbon (25 mg, 0.023 mmol) in ethanol (20 mL) is stirred at room temperature under a hydrogen balloon for 16 h. The reaction is filtered through a pad of diatomaceous earth and the filtrate is concentrated in vacuo to give the title compound as a colorless oil (1.0 g, 88%). LC-ES/MS m/z 218 (M+1).

후처리

  1. filtrationThe reaction is filtered through a pad of diatomaceous earth
  2. concentrationthe filtrate is concentrated in vacuo

출처 및 근거

ORD 기록
ord-5927bea749aa4b8e977395af7c8dda26
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658693B2

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