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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572715Generated: October 26, 2026

Methanol → Methyl 3-acetyl-5-bromo-4-hydroxybenzoate

https://huagongshe.com/reaction/572715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Acetyl-5-bromo-4-hydroxybenzoic acidHCID 12486469—
ProductMethyl 3-acetyl-5-bromo-4-hydroxybenzoateHCID 1581898042.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred suspension of 3-acetyl-5-bromo-4-hydroxybenzoic acid (240 g, 926 mmol) in MeOH (2 L) was added dropwise sulfurous dichloride (68 mL, 926.5 mmol) under nitrogen and the mixture was heated at 80° C. for 3 h. The reaction mixture was cooled to room temperature concentrated, diluted with DCM. The organic layer was washed with brine, dried over magnesium sulfate, filtered and concentrated to afford a crude compound, which was purified on silica, eluting with 70% of DCM in petroleum ether. The solvents were evaporated to dryness to afford methyl 3-acetyl-5-bromo-4-hydroxybenzoate (108 g, 42.7%) as a white powder. Mass Spectrum: [M−H]− 229.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029374B2
Source datasetuspto-grants-2015_05
ORD IDord-48d6b429481a4dc8948ef82bfaaed62c
Source noteuspto-grants-2015_05