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

N-bromobutanimide → 5-Bromo-3-(bromomethyl)-1-benzothiophene

HRID 481976
노트
인쇄 미리보기

반응식

HRID 481976 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[C:7]([CH3:10])[C:6]=2[CH:11]=1.[Br:12]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[C:7]([CH2:10][Br:12])[C:6]=2[CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 67184N-bromobutanimideHCID 141757645-Bromo-3-methyl-1-benzothiophene

생성물 1

HCID 217904115-Bromo-3-(bromomethyl)-1-benzothiophene수율 74%

시약·촉매·용매 2

HCID 7187Benzoyl Peroxide촉매HCID 5943Carbon Tetrachloride용매

실험 절차

A solution of 4.30 gm (18.9 mMol) 5-bromo-3-methylbenzothiophene, 0.25 gm (1.03 mMol) benzoylperoxide, and 3.37 gm (18.9 mMol) N-bromosuccinimide in 50 mL carbon tetrachloride was heated at reflux for 3 hours. The reaction mixture was cooled to room temperature, filtered and the filtrate concentrated under reduced pressure. The residue was subjected to flash silica gel chromatography, eluting with hexane. Fractions containing the desired compound were combined and concentrated under reduced pressure to provide 4.28 gm (74%) of the desired compound.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureat reflux for 3 hours
  2. filtrationfiltered
  3. concentrationthe filtrate concentrated under reduced pressure
  4. washeluting with hexane
  5. additionFractions containing the desired compound
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-776cab91e17c4389b641455b46db93a8
출처 데이터셋
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05792763

반응 노트

불러오는 중…