Реакция #549672

ord-9294cf4daf074f6bb93834a22e447873

Уравнение реакции

N#[N+]c1ccc(Cl)cc1.[Cl-]
p-chlorobenzenediazonium chloride
N#[N+]c1cccc(Cl)c1.[Cl-]
m-chlorobenzenediazonium chloride
Cc1cccc([N+]#N)c1.[Cl-]
m-toluenediazonium chloride

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеvery variable yields of between 40 and 85% of theory
  2. 2
    Другоеare obtained

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04515940uspto-grants-1985_05