Benzenediazonium, 3-chloro-, chloride → m-Toluenediazonium chloride

HRID 462490ノート

反応式

HRID 462490 の反応式
[Cl-].[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]#[N:10])=[CH:5][CH:4]=1.[Cl-].Cl[C:13]1C=C([N+]#N)C=CC=1>>[Cl-:2].[C:8]1([CH3:13])[CH:3]=[CH:4][CH:5]=[C:6]([N+:9]#[N:10])[CH:7]=1

参加物

3

実験手順

When these processes are repeated using variously substituted aryldiazonium salts, very variable yields of between 40 and 85% of theory are obtained. For example, p-chlorobenzenediazonium chloride gives 43%, m-chlorobenzenediazonium chloride gives 36%, m-toluenediazonium chloride gives 69%, o-chlorobenzenediazonium chloride gives 36%, p-dimethylaminobenzenediazonium chloride gives 54%, p-carbamoylbenzenediazonium chloride gives 58%, benzenediazonium chloride gives 72%, p-methoxybenzenediazonium chloride gives 80% and p-sulfobenzenediazonium chloride gives 10 to 20% of the corresponding diazosulfonate.

後処理

  1. customvery variable yields of between 40 and 85% of theory
  2. customare obtained

出典と根拠

ORDレコード
ord-9294cf4daf074f6bb93834a22e447873
出典データセット
uspto-grants-1985_05
特許番号
US04515940

反応ノート

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