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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863141Generated: October 30, 2026

3-Bromo-2-hydroxy-6-methoxybenzoic acid → 2-Bromo-5-methoxyphenol

https://huagongshe.com/reaction/863141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-2-hydroxy-6-methoxybenzoic acidHCID 13493838—
SolventQuinolineHCID 7047—
Product2-Bromo-5-methoxyphenolHCID 13493839—

Reaction Steps

3-Bromo-2-hydroxy-6-methoxybenzoic acid [T. de Paulis el. al. J. Med. Chem., (1985), 28, 1263-1269] (5 g; 0.02 mol) was heated in quinoline (200 mL) at 160° C. for 1 h. On cooling, the product was partitioned between Et2O and 3M HCl. The organic extract was washed with water and brine then dried (MgSO4), filtered and evaporated to give the title compound which was recrystallized from 5% ethyl acetate/hexane (4 g, 97%); m.p. 40°-42° C. Anal. Calc. for C7H7 BrO2 : C, 41.41; H, 3.48. Found C, 41.39; H, 3.37.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719183
Source datasetuspto-grants-1998_02
ORD IDord-10027fad20ca44078c9b4ac60d92ee6c
Source noteuspto-grants-1998_02