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Hydrogen Bromide → 2-Bromo-1-(4-hydroxy-3-(hydroxymethyl)phenyl)ethan-1-one

HRID 367330
ノート
印刷プレビュー

反応式

HRID 367330 の反応式
C([O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11](=[O:14])[CH2:12][Br:13])=[CH:7][C:6]=1[CH2:15][O:16]C(=O)C)(=O)C.Br.O>CO>[Br:13][CH2:12][C:11]([C:8]1[CH:9]=[CH:10][C:5]([OH:4])=[C:6]([CH2:15][OH:16])[CH:7]=1)=[O:14]
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 260Hydrogen BromideHCID 962WaterHCID 112788962-Acetoxy-5-(2-bromoacetyl)benzyl acetate

生成物 1

HCID 113340552-Bromo-1-(4-hydroxy-3-(hydroxymethyl)phenyl)ethan-1-one収率 68.9%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

2-Acetoxymethyl-4-bromoacetylphenyl acetate (18.6 g) was dissolved in 90 ml of methanol, 100 ml of 47% hydrobromic acid was added with stirring under ice-cooling, and the mixture was subjected to 16 hours of reaction at room temperature. Water was added to the reaction solution with stirring under ice-cooling, and the resulting precipitates were collected by filtration and washed with water and hexane to give 9.54 g of 2-bromo-4'-hydroxy-3'-hydroxymethylacetophenone having a melting point of 117 to 119° C.

後処理

  1. temperaturecooling
  2. customthe mixture was subjected to 16 hours of reaction at room temperature
  3. stirringwith stirring under ice-
  4. temperaturecooling
  5. customthe resulting precipitates
  6. filtrationwere collected by filtration
  7. washwashed with water and hexane

出典と根拠

ORDレコード
ord-e86e760ef26a46c2a17e06cc180d55e1
出典データセット
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06133266

反応ノート

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