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

Imidazole → 2-Bromo-5-chloro-3-t-butyldimethylsilyloxy-methylbenzene

HRID 1081886
노트
인쇄 미리보기

반응식

HRID 1081886 반응식
[Br:1][C:2]1[CH:9]=[CH:8][C:7]([Cl:10])=[CH:6][C:3]=1[CH2:4]O.N1C=CN=C1.[C:16]([Si:20](Cl)([CH3:22])[CH3:21])([CH3:19])([CH3:18])[CH3:17].CN(C=[O:28])C>CCOCC>[Br:1][C:2]1[C:9]([O:28][Si:20]([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:22])[CH3:21])=[CH:8][C:7]([Cl:10])=[CH:6][C:3]=1[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 795ImidazoleHCID 6228Dimethylformamide2회HCID 28928tert-Butyldimethylsilyl chlorideHCID 23363134(2-Bromo-5-chlorophenyl)methanol

생성물 1

HCID 540356052-Bromo-5-chloro-3-t-butyldimethylsilyloxy-methylbenzene

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To the solution of 2-bromo-5-chlorobenzylalcohol (10 g) from Example 73 and imidazole (3.23 g) in dry DMF (50ml) was added dropwise t-butyl chloro dimethylsilane in dry DMF (10 ml) for 20 minutes at -0° C. After addition, the mixture was stirred for 30 minutes at room temperature. The mixture was diluted with ether, and washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate.

후처리

  1. additionAfter addition
  2. washwashed with saturated sodium chloride solution
  3. dry with materialdried over anhydrous sodium sulfate

출처 및 근거

ORD 기록
ord-88b7559467854c518a0df0ac0ab495bd
출처 데이터셋
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05587392

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트