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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862347Generated: October 30, 2026

3-Bromo-2-hydroxy-6-methoxybenzoic acid → 1-Bromo-4-methoxy-2-(methoxymethoxy)benzene

https://huagongshe.com/reaction/862347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-2-hydroxy-6-methoxybenzoic acidHCID 13493838—
Reactant2-Bromo-5-methoxyphenolHCID 13493839—
SolventQuinolineHCID 7047—
Product1-Bromo-4-methoxy-2-(methoxymethoxy)benzeneHCID 14827037—

Reaction Steps

1-Bromo-2-hydroxy-4-methoxybenzene. 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 C7H7BrO2 : C, 41.41; H, 3.48. Found C, 41.39; H, 3.37.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716984
Source datasetuspto-grants-1998_02
ORD IDord-b229ba1c7cc745c7a538fe83f9726d27
Source noteuspto-grants-1998_02