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Bromine → 5-(2-Bromoacetyl)-1,3-phenylene diacetate

HRID 1489231
ノート
印刷プレビュー

反応式

HRID 1489231 の反応式
[C:1]([O:4][C:5]1[CH:6]=[C:7]([C:15](=[O:17])[CH3:16])[CH:8]=[C:9]([O:11][C:12](=[O:14])[CH3:13])[CH:10]=1)(=[O:3])[CH3:2].[Br:18]Br>C(=S)=S>[C:12]([O:11][C:9]1[CH:8]=[C:7]([C:15](=[O:17])[CH2:16][Br:18])[CH:6]=[C:5]([O:4][C:1](=[O:3])[CH3:2])[CH:10]=1)(=[O:14])[CH3:13]
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 24408BromineHCID 6880155-Acetyl-1,3-phenylene diacetate

生成物 1

HCID 187073195-(2-Bromoacetyl)-1,3-phenylene diacetate

試薬・触媒・溶媒 1

HCID 6348Carbon Disulfide溶媒2 回

反応条件

温度
50 °C

実験手順

4 g of 3',5'-diacetyloxyacetophenone was suspended in 75 ml of carbon disulfide. Thereto was dropwise added a solution of 0.90 ml of bromine dissolved in 25 ml of carbon disulfide, at room temperature in about 1 hour. The system was heated to about 50° C. ocassionally in the course of dropwise addition and, each time when a reaction started, the system was returned to room temperature and stirred. After the completion of the dropwise addition, stirring was conducted at room temperature for 1 hour. After the completion of the reaction, the solvent was removed by distillation to obtain 5.53 g of 3',5'-diacetyloxy-2-bromoacetophenone as brown crystals.

後処理

  1. customwas returned to room temperature
  2. additionAfter the completion of the dropwise addition
  3. stirringstirring
  4. customAfter the completion of the reaction
  5. customthe solvent was removed by distillation

出典と根拠

ORDレコード
ord-42f53206acda404c90c0e4fc2a182575
出典データセット
uspto-grants-1997_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05677319

反応ノート

読み込み中…

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