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

Azidotrimethylsilane → 1-(2-Azido-2-methylpropyl)-4-(trifluoromethyl)benzene

HRID 244953
노트
인쇄 미리보기

반응식

HRID 244953 반응식
[CH3:1][C:2](O)([CH3:14])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][CH:5]=1.C[Si]([N:20]=[N+:21]=[N-:22])(C)C>C(Cl)Cl>[N:20]([C:2]([CH3:14])([CH3:1])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][CH:5]=1)=[N+:21]=[N-:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 78378AzidotrimethylsilaneHCID 651450142-Methyl-1-(4-(trifluoromethyl)phenyl)propan-2-ol

생성물 1

HCID 866974731-(2-Azido-2-methylpropyl)-4-(trifluoromethyl)benzene수율 86.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

26.3 g of 2-methyl-1-(4-(trifluoromethyl)phenyl)propan-2-ol was dissolved in 400 mL of methylene chloride, and 25 mL (0.19 mol) of trimethylsilyl azide and 24 mL (0.19 mol) of boron trifluoride diethyl ether complex were added dropwise under cooling with ice. The reaction mixture was stirred at room temperature for 20 hours. After completion of the reaction, the reaction mixture was washed with saturated aqueous sodium hydrogen carbonate and with saturated aqueous sodium chloride successively, dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to give 25.4 g of the desired product.

후처리

  1. temperatureunder cooling with ice
  2. customAfter completion of the reaction
  3. washthe reaction mixture was washed with saturated aqueous sodium hydrogen carbonate and with saturated aqueous sodium chloride successively
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-7c0bfcfffe2043caa376f8bc7bfa3f62
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658686B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트