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Diethyl Ether → 1-(Benzyloxy)-2-bromo-4-(trifluoromethyl)benzene

HRID 269531
ノート
印刷プレビュー

反応式

HRID 269531 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([C:9]([F:12])([F:11])[F:10])[CH:5]=[CH:6][C:7]=1[OH:8].[CH2:13](Br)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C(=O)([O-])[O-].[K+].[K+].C(OCC)C>CC(C)=O.O>[CH2:13]([O:8][C:7]1[CH:6]=[CH:5][C:4]([C:9]([F:10])([F:11])[F:12])=[CH:3][C:2]=1[Br:1])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 3283Diethyl EtherHCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 27611682-Bromo-4-(trifluoromethyl)phenol

生成物 1

HCID 187826691-(Benzyloxy)-2-bromo-4-(trifluoromethyl)benzene収率 85%

試薬・触媒・溶媒 2

HCID 180Acetone溶媒
HCID 962Water溶媒

実験手順

A solution of 3-bromo-4-hydroxybenzotrifluoride (6.03 g, 25 mmol) in acetone (1000 ml) was treated with benzyl bromide (4.67 g, 3.25 ml, 27.5 mmol) and potassium carbonate (5.18 g, 37.5 mmol). The mixture was stirred and heated to reflux under nitrogen for 2 h. After cooling, diethyl ether (300 ml) and water (300 ml) were added and the aqueous phase re-extracted with diethyl ether (100 ml). The combined organic layers were washed with water, dried (MgSO4) and the solvent removed in vacuo. The orange oil was flash chromatographed (silica gel, 2-5% dichloromethane-isohexane) to give the title compound as a clear oil (7.0 g, 85%).

後処理

  1. temperatureheated
  2. temperatureto reflux under nitrogen for 2 h
  3. temperatureAfter cooling
  4. extractionthe aqueous phase re-extracted with diethyl ether (100 ml)
  5. washThe combined organic layers were washed with water
  6. dry with materialdried (MgSO4)
  7. customthe solvent removed in vacuo
  8. customchromatographed (silica gel, 2-5% dichloromethane-isohexane)

出典と根拠

ORDレコード
ord-b3c7d4e19f464c9d9bd9ce4f7a4b83aa
出典データセット
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07446222B2

反応ノート

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