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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399236Generated: October 26, 2026

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

https://huagongshe.com/reaction/399236

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 et. 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 numberUS05817693
Source datasetuspto-grants-1998_10
ORD IDord-53bfd2b8127647178abb10b7c1bcea7e
Source noteuspto-grants-1998_10