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

4-Fluorothiophenol → 4-Bromo-1-{[(4-fluorophenyl)sulfanyl]methyl}-2-nitrobenzene

HRID 1988900
노트
인쇄 미리보기

반응식

HRID 1988900 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8]Br)=[C:4]([N+:10]([O-:12])=[O:11])[CH:3]=1.[F:13][C:14]1[CH:19]=[CH:18][C:17]([SH:20])=[CH:16][CH:15]=1.C(N(C(C)C)CC)(C)C>O1CCCC1>[F:13][C:14]1[CH:19]=[CH:18][C:17]([S:20][CH2:8][C:5]2[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][C:4]=2[N+:10]([O-:12])=[O:11])=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 677894-FluorothiophenolHCID 81531DiisopropylethylamineHCID 127613784-Bromo-1-(bromomethyl)-2-nitrobenzene

생성물 1

HCID 586564724-Bromo-1-{[(4-fluorophenyl)sulfanyl]methyl}-2-nitrobenzene

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 4-bromo-1-(bromomethyl)-2-nitrobenzene (0.60 g) in tetrahydrofuran (10 ml) was added 4-fluorothiophenol (1.2 ml) and diisopropylethylamine (0.45 ml). After stirring for 2 h the mixture was concentrated under vacuum and purified by column chromatography on silica, eluting with petroleum ether (40-60°):dichloromethane (9:1 to 8:1) to give the title compound (0.52 g).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. concentrationwas concentrated under vacuum
  2. custompurified by column chromatography on silica
  3. washeluting with petroleum ether (40-60°)

출처 및 근거

ORD 기록
ord-f40a363831074b65b40a55e21fce8045
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07642276B2

반응 노트

불러오는 중…