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

Propargyl bromide → 1-Bromo-4-fluoro-2-[(prop-2-yn-1-yl)oxy]benzene

HRID 618719
노트
인쇄 미리보기

반응식

HRID 618719 반응식
[CH2:1](Br)[C:2]#[CH:3].[Br:5][C:6]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][C:7]=1[OH:13].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[Br:5][C:6]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][C:7]=1[O:13][CH2:3][C:2]#[CH:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7842Propargyl bromideHCID 11430Potassium CarbonateHCID 27246002-Bromo-5-fluorophenol

생성물 1

HCID 224828471-Bromo-4-fluoro-2-[(prop-2-yn-1-yl)oxy]benzene수율 97.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

A solution of 42.95 g (0.36 mol) of propargyl bromide in 30 ml of dimethylformamide was added dropwise to a suspension of 50 g (0.26 mol) of 2-bromo-5-fluoro-phenol and 55 g of potassium carbonate in 300 ml of dimethylformamide and the mixture was subsequently stirred at room temperature for two hours. The mixture was poured on to 1500 ml of ice-water and extracted three times with 600 ml of dichloromethane each time. After drying over sodium sulfate concentration was carried out in a vacuum. The crude product obtained was purified by column chromatography on silica gel (dichloromethane/hexane 1:1). 58 g (97%) of 1-bromo-4-fluoro-2-prop-2-ynyloxy-benzene were obtained as a pale yellow oil.

후처리

  1. extractionextracted three times with 600 ml of dichloromethane each time
  2. dry with materialAfter drying over sodium sulfate concentration
  3. customThe crude product obtained
  4. customwas purified by column chromatography on silica gel (dichloromethane/hexane 1:1)

출처 및 근거

ORD 기록
ord-e06e1d0fcf2b4010b0fc694fbb639c2d
출처 데이터셋
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05955495

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트