Facile preparations of 4-fluororesorcinol
- 1 June 1988
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 66 (6) , 1479-1482
- https://doi.org/10.1139/v88-238
Abstract
Two facile methods for preparing 4-fluororesorcinol have been developed. In the first method, the direct fluorination of 1,3-dimethoxybenzene with trifluoromethyl hypofluorite carried out in Freon 11 at −78 °C afforded 2,4-dimethoxyfluorobenzene. Demethylation by heating under reflux in 48% HBr in acetic acid gave 4-fluororesorcinol in an overall yield of 60%. The second method involved the fluorination of 2,6-dimethoxyacetophenone by trifluoromethyl hypofluorite in Freon 11 at −78 °C, leading to 2,6-dimethoxy-3-fluoroacetophenone. On heating under reflux in 48% HBr in acetic acid, 4-fluororesorcinol was obtained in an overall yield of 74%. The latter is the method of choice for preparing 4-fluororesorcinol.This publication has 1 reference indexed in Scilit:
- A novel electrophilic fluorination of activated aromatic rings using acetyl hypofluorite, suitable also for introducing fluorine-18 into benzeneThe Journal of Organic Chemistry, 1984