Migration of halogen atoms in halogenoderivatives of 2,4‐dihydroxypyridine (I)
- 1 January 1951
- journal article
- research article
- Published by Wiley in Recueil des Travaux Chimiques des Pays-Bas
- Vol. 70 (4), 353-360
- https://doi.org/10.1002/recl.19510700410
Abstract
When 3‐bromo‐2,4‐dihydroxypyridine is chlorinated in aqueous hydrochloric acid solution by adding hydrogen peroxide solution, 5‐bromo‐3‐chloro‐2,4‐dihydroxypyridine is formed. Hence the chlorine atom enters the 3‐position, the bromine atom being removed from this position and reintroduced at the 5‐position.5‐Bromo‐3‐chloro‐2,4‐dihydroxypyridine was also prepared by brominating 3‐chloro‐2,4‐dihydroxypyridine and chlorinating 5‐bromo‐2,4‐dihydroxypyridine. Its structure was established in different ways, i. e. by converting it into 3‐chloro‐2,4‐dihydroxypyridine on partial reduction, by converting it into 4‐amino‐2,3‐dichloro‐5‐bromopyridine and into 4‐amino‐2,5‐dibromo‐3‐chloropyridine. The structure of the two compounds last mentioned was proved by synthesis.This publication has 2 references indexed in Scilit:
- The chloropyridinesRecueil des Travaux Chimiques des Pays-Bas, 1950
- On bromopyridines: (59th communication on derivatives of pyridine and quinoline)Recueil des Travaux Chimiques des Pays-Bas, 1945