홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Imidazole → 2-(3-Tert-butyldimethylsilyloxyprop-2-enyl)nitrobenzene

HRID 1106935
노트
인쇄 미리보기

반응식

HRID 1106935 반응식
[C:1]([Si:5]([CH3:8])([CH3:7])Cl)([CH3:4])([CH3:3])[CH3:2].[N+:9]([C:12]1[CH:21]=[CH:20][CH:19]=[CH:18][C:13]=1[CH:14]=[CH:15][CH2:16][OH:17])([O-:11])=[O:10].N1C=CN=C1>CN(C=O)C>[Si:5]([O:17][CH:16]=[CH:15][CH2:14][C:13]1[CH:18]=[CH:19][CH:20]=[CH:21][C:12]=1[N+:9]([O-:11])=[O:10])([C:1]([CH3:4])([CH3:3])[CH3:2])([CH3:8])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 533957172-Nitrocinnamyl alcohol

생성물 1

HCID 544712302-(3-Tert-butyldimethylsilyloxyprop-2-enyl)nitrobenzene

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Tert-butyldimethylchlorosilane (5.10 g, 33.8 mmol) was added to a solution of 2-nitrocinnamyl alcohol (5.05 g, 28.2 mmol) and imidazole (2.88 g, 42.3 mmol) in DMF (100 ml). After stirring at room temperature for 18 hours the reaction mixture was partitioned between water (200 ml) and ethyl acetate (200 ml). The organic layer was separated washed with brine (2×m 100 ml) and dried (MgSO4). Filtration and evaporation of the solvent gave the crude product which was purified by flash chromatography on silica gel with ethyl acetate-hexane (1:3) as eluant. (7.82 g, 95%).

후처리

  1. customwas partitioned between water (200 ml) and ethyl acetate (200 ml)
  2. customThe organic layer was separated
  3. washwashed with brine (2×m 100 ml)
  4. dry with materialdried (MgSO4)
  5. filtrationFiltration and evaporation of the solvent

출처 및 근거

ORD 기록
ord-0c430a21c3624f98b5b22922ad7c68ea
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06057311

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트