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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051064Generated: November 1, 2026

Acetyl chloride → Methyl 3-bromo-5-hydroxybenzoate

https://huagongshe.com/reaction/1051064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant3-Bromo-5-hydroxybenzoic acidHCID 15735511—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-bromo-5-hydroxybenzoateHCID 5321660798.8%

Reaction Steps

To a flask containing 3-bromo-5-hydroxybenzoic acid (2.0 g, 9.2 mmol) in anhydrous MeOH (10 mL) at 0° C. under N2 was added AcCl (912 μL, 12.9 mmol). The reaction mixture was allowed to warm to room temperature overnight. The mixture was diluted with EA and washed with NaHCO3. The organic layers were dried and concentrated to provide 2.1 g (97%) of methyl 3-bromo-5-hydroxybenzoate as a white solid. LCMS-ESI (m/z) calculated for C8H7BrO3: 231.04. found 232.9 [M+H]+, tR=3.06 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388147B2
Source datasetuspto-grants-2016_07
ORD IDord-6e455b4139de435d90538567cb120cc0
Source noteuspto-grants-2016_07