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

Chlorotrimethylsilane → 3-(Trimethylsilyl)benzenemethanol

HRID 1938572
노트
인쇄 미리보기

반응식

HRID 1938572 반응식
Br[C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][OH:6].C([Li])CCC.[CH3:15][Si:16](Cl)([CH3:18])[CH3:17]>C(OCC)C>[CH3:15][Si:16]([CH3:18])([CH3:17])[C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][OH:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6397ChlorotrimethylsilaneHCID 851413-Bromobenzyl alcoholHCID 178418339Butyllithium

생성물 1

HCID 151146973-(Trimethylsilyl)benzenemethanol

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

To a solution of 3-bromobenzylalcohol (9.35 g, 50 mmol) in diethyl ether (50 ml) at 0° C. was added dropwise 1.5M butyllithium (66.7 ml) and the mixture was stirred 30 min. Then trimethylsilylchloride (11.39 g, 105 mmol) in diethyl ether (50 ml) was added dropwise and the mixture was stirred at room temperature 18 hours. The reaction mixture was treated with ice water (100 ml) and the organic layer extracted, washed with water, brine, dried over MgSO4 and concentrated. The crude product was dissolved in 90% aqueous methanol (100 ml) and refluxed 1 hour. The solvents were removed and 3-trimethylsilylbenzylalcohol was purified by distillation.

후처리

  1. stirringthe mixture was stirred at room temperature 18 hours
  2. extractionthe organic layer extracted
  3. washwashed with water, brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. dissolutionThe crude product was dissolved in 90% aqueous methanol (100 ml)
  7. temperaturerefluxed 1 hour
  8. customThe solvents were removed
  9. distillation3-trimethylsilylbenzylalcohol was purified by distillation

출처 및 근거

ORD 기록
ord-dc0edb14b0fe487489c4fc76b3432e11
출처 데이터셋
uspto-grants-1997_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05693668

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트