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Boron tribromide dichloromethane → 4-Chloro-2-(2-phenylethenyl)phenol

HRID 644448
ノート
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反応式

HRID 644448 の反応式
B(Br)(Br)Br.ClCCl.[Cl:8][C:9]1[CH:10]=[CH:11][C:12]([O:23]C)=[C:13]([CH:22]=1)[CH:14]=[CH:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>ClCCl.C(OCC)(=O)C>[Cl:8][C:9]1[CH:10]=[CH:11][C:12]([OH:23])=[C:13]([CH:14]=[CH:15][C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:22]=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 2

HCID 22277759Boron tribromide dichloromethaneHCID 685787655-Chloro-2-methoxy-beta-phenylstyrene

生成物 1

HCID 685807274-Chloro-2-(2-phenylethenyl)phenol収率 49.4%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 8857Ethyl Acetate溶媒

実験手順

Under argon atmosphere, 1 mol/L boron tribromide/dichloromethane solution (0.5 mL, 0.5 mmol) was added to a solution of 5-chloro-2-methoxy-β-phenylstyrene (80 mg, 0.3 mmol) in dichloromethane (2 mL) at room temperature, and the mixture was stirred for 12 hours. The reaction mixture was diluted with ethyl acetate (15 mL), and after it was washed successively with water and brine, dried over anhydrous sodium sulfate, the residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (34.2 mg, 45.4%) as a white powder.

後処理

  1. washafter it was washed successively with water and brine
  2. dry with materialdried over anhydrous sodium sulfate
  3. customthe residue obtained by evaporation of the solvent under reduced pressure
  4. customwas purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1)

出典と根拠

ORDレコード
ord-ddae2e34a715429fa32f65a3b9ff0584
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07700655B2

反応ノート

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