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

Benzene → N,N-bis(trimethylsilyl)Methanesulfonamide

HRID 974378
노트
인쇄 미리보기

반응식

HRID 974378 반응식
[CH3:1][S:2]([NH2:5])(=[O:4])=[O:3].C(N(CC)CC)C.C1C=CC=CC=1.[CH3:19][Si:20]([CH3:23])([CH3:22])Cl>CCCCCC>[CH3:19][Si:20]([CH3:23])([CH3:22])[N:5]([Si:20]([CH3:23])([CH3:22])[CH3:19])[S:2]([CH3:1])(=[O:4])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 241BenzeneHCID 6397ChlorotrimethylsilaneHCID 8471TriethylamineHCID 72879Methanesulfonamide2회

생성물 1

HCID 12503736N,N-bis(trimethylsilyl)Methanesulfonamide

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

A glass reactor equipped with a stirrer, nitrogen inlet, reflux condenser and addition funnel was purged with nitrogen and charged with 29.1 g (0.30 mol) of methanesulfonamide, MeSO2NH2, where Me represents the methyl radical, 84.9 ml (0.605 mol) of triethylamine and 240 ml of dry benzene. Trimethylchlorosilane (129.5 ml, 1.00 mol) was then added through the addition funnel over a period of 15 minutes to the stirred mixture, followed by heating at the boiling point for three hours. The mixture was then diluted with 200 ml of hexane and stirring was continued for 30 minutes.

후처리

  1. customA glass reactor equipped with a stirrer, nitrogen inlet
  2. temperaturereflux
  3. additioncondenser and addition funnel
  4. customwas purged with nitrogen
  5. temperatureby heating at the boiling point for three hours

출처 및 근거

ORD 기록
ord-abc4716cdac84c6f91c8dbce364af083
출처 데이터셋
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05068379

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트