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

HRID 618719
ノート
印刷プレビュー

反応式

HRID 618719 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-e06e1d0fcf2b4010b0fc694fbb639c2d
出典データセット
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05955495

反応ノート

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