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Boron tribromide → 2-(2,2,2-Trifluoroethoxy)phenol

HRID 273848
ノート
印刷プレビュー

反応式

HRID 273848 の反応式
C[O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[O:9][CH2:10][C:11]([F:14])([F:13])[F:12].B(Br)(Br)Br.C(=O)(O)[O-].[Na+]>C(Cl)Cl>[F:12][C:11]([F:13])([F:14])[CH2:10][O:9][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=1[OH:2]
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 25134Boron tribromideHCID 516892Sodium BicarbonateHCID 200943441-Methoxy-2-(2,2,2-trifluoroethoxy)benzene

生成物 1

HCID 130853472-(2,2,2-Trifluoroethoxy)phenol収率 66.4%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 1-methoxy-2-(2,2,2-trifluoroethoxy)benzene (3.83 g) in dry methylene chloride (50 ml) was added boron tribromide (3.1 ml) with stirring under ice cooling, and the mixture was reacted for 30 minutes. The reaction mixture was poured into an aqueous sodium bicarbonate solution (500 ml), and the mixture was extracted with diethyl ether. The extract was washed with water, dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by medium pressure liquid column chromatography on silica gel using a mixture of hexane and diethyl ether (20/1) as eluent to give 2.37 g of 2-(2,2,2-trifluoroethoxy)phenol melting at 49°-50° C.

後処理

  1. customthe mixture was reacted for 30 minutes
  2. extractionthe mixture was extracted with diethyl ether
  3. washThe extract was washed with water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customThe solvent was evaporated under reduced pressure
  6. customthe residue was purified by medium pressure liquid column chromatography on silica gel using
  7. additiona mixture of hexane and diethyl ether (20/1) as eluent

出典と根拠

ORDレコード
ord-5f857da3779642d896d4eac20503ac1d
出典データセット
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05387603

反応ノート

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