Hofmann rearrangement
id:
hofmann-rearrangement-169-11937396
title:
Hofmann rearrangement
text:
The Hofmann rearrangement is the organic reaction of a primary amide to a primary amine with one less carbon atom. The reaction involves oxidation of the nitrogen followed by rearrangement of the carbonyl and nitrogen to give an isocyanate intermediate. The reaction can form a wide range of products, including alkyl and aryl amines. The reaction is named after its discoverer, August Wilhelm von Hofmann, and should not be confused with the Hofmann elimination, another name reaction for which he i
brand slug:
wiki
category slug:
encyclopedia
description:
Type of chemical reaction
original url:
https://en.wikipedia.org/wiki/Hofmann_rearrangement
date created:
2005-03-09T02:31:32Z
date modified:
2024-08-31T23:55:11Z
main entity:
{"identifier":"Q537681","url":"https://www.wikidata.org/entity/Q537681"}
image:
fields total:
13
integrity:
15