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1-Phenyl-1,2-propanedione → 3-Bromo-1-phenylpropane-1,2-dione

HRID 236286
ノート
印刷プレビュー

反応式

HRID 236286 の反応式
[C:1]1([C:7](=[O:11])[C:8](=[O:10])[CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:12]Br>C(Cl)(Cl)Cl>[Br:12][CH2:9][C:8](=[O:10])[C:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)=[O:11]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 113631-Phenyl-1,2-propanedioneHCID 24408Bromine2 回

生成物 1

HCID 125689113-Bromo-1-phenylpropane-1,2-dione収率 102%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

反応条件

温度
50 °C

実験手順

5.32 kg of 1-phenylpropane-1,2-dione (98.6% by G.C. equivalent to 5.24 kg, 35.4 mole) were dissolved in 36 liters of chloroform and the solution was heated to 50° C. A solution of 5.66 kg (35.4 mole) of bromine in 8 liters of chloroform was added slowly to maintain a gentle reflux and immediate decolorization of the bromine (approximately 6 hours). The solution was cooled to room temperature overnight and was washed with 20 liters of saturated sodium bicarbonate solution and 20 liters of water and dried over sodium sulfate. The solvent was removed under vacuum to obtain 8.2 kg (100% yield) of a green/yellow oil which was used directly for subsequent reactions after estimation of its purity (approximately 75% by G.C. or N.M.R.).

後処理

  1. temperatureto maintain
  2. temperaturea gentle reflux
  3. temperatureThe solution was cooled to room temperature overnight
  4. washwas washed with 20 liters of saturated sodium bicarbonate solution and 20 liters of water
  5. dry with materialdried over sodium sulfate
  6. customThe solvent was removed under vacuum

出典と根拠

ORDレコード
ord-501fe104ed934cbc80f2252f8a7f9dfa
出典データセット
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04643999

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート