## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
An expedient esterification of aromatic carboxylic acids using sodium bromate and sodium hydrogen sulfite
β Scribed by Khalid Mohammed Khan; Ghulam Murtaza Maharvi; Safdar Hayat; Zia-Ullah; M. Iqbal Choudhary; Atta-ur-Rahman
- Book ID
- 104205463
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 145 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
Treatment of aromatic carboxylic acids and substituted toluenes with a mixture of sodium bromate and sodium hydrogen sulfite in a two-phase system gave the corresponding esters in good yield. The intermediate a-brominated toluene was formed by the in situ generated hypobromous acid. The a-bromotoluene underwent an intermolecular nucleophilic substitution reaction with aromatic carboxylic acids present in the reaction mixture to afford the corresponding esters.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Acyloxyboron intermediates formed in situ from carboxylic acids and 3,4,5-trifluorophenylboronic acids react with sodium borohydride in THF to give alcohols in good to high yields.