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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Benzoyl chloride → Benzophenone

HRID 1404821
ノート
印刷プレビュー

反応式

HRID 1404821 の反応式
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1OCCC.[Cl-].[Al+3].[Cl-].[Cl-].[C:16](Cl)(=[O:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>ClCCl>[C:16]([C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)(=[O:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1
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

5

反応物 3

HCID 7412Benzoyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 179525341-bromo-2-propoxybenzene

生成物 1

HCID 3102Benzophenone

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

69.7 g (324.2 mmol) of 1-bromo-2-propoxybenzene was added dropwise to a dichloromethane (350 ml) solution containing 51.8 g (388.6 mmol) of aluminum chloride and 45.6 g (324.3 mmol) of benzoyl chloride which was cooled to 0° C. After addition, the resulting solution was stirred for 2 hours. After a reaction, the reaction solution was washed with water, the solvent was removed, and the obtained product was purified by column chromatography to obtain a benzophenone derivative represented by the following formula (40) as 67.3 g (210.7 mmol, yield of 65%) of a yellow solid.

後処理

  1. additionAfter addition
  2. customAfter a reaction
  3. washthe reaction solution was washed with water
  4. customthe solvent was removed
  5. customthe obtained product was purified by column chromatography

出典と根拠

ORDレコード
ord-9926d0e570904e2fae3734196513106c
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08916071B2

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