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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572714Generated: November 1, 2026

Hydrochloric Acid → Methyl 4-acetoxy-3-bromobenzoate

https://huagongshe.com/reaction/572714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantMethyl 3-bromo-4-hydroxybenzoateHCID 4778958—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-acetoxy-3-bromobenzoateHCID 4503703394.1%

Reaction Steps

To a stirred suspension of methyl 3-bromo-4-hydroxybenzoate (270 g, 1168 mmol) in DCM (1.5 L) was added pyridine (150 mL). Acetyl chloride (87 mL, 1227 mmol) was then added dropwise at room temperature and under nitrogen. The mixture was left to stir for 2 hrs at room temperature. Water (1 L) was then added followed by HCl 2N until pH 1. The organic layer was then washed with water, brine, dried over magnesium sulfate, filtered and evaporated to dryness to afford methyl 4-acetoxy-3-bromobenzoate (300 g, 94%) as a white powder. NMR Spectrum: (DMSOd6) 2.34 (s, 3H), 3.87 (s, 3H), 7.47 (d, 1H), 8.01 (dd, 1H), 8.20 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029374B2
Source datasetuspto-grants-2015_05
ORD IDord-1d970a982c79410db527caef19bb9f82
Source noteuspto-grants-2015_05