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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042350Generated: October 31, 2026

Methanol → Methyl 3-bromo-2-methoxybenzoate

https://huagongshe.com/reaction/1042350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-Bromo-2-methoxybenzoic acidHCID 253598—
CatalystSulfuric AcidHCID 1118—
ProductMethyl 3-bromo-2-methoxybenzoateHCID 46311082—

Reaction Steps

Approximately two drops of sulfuric acid were added to a solution of 3-bromo-2-methoxy-benzoic acid (10.00 g, 43.30 mmol) in methanol and the resulting reaction mixture was refluxed for 14 hours. The reaction mixture was cooled to room temperature, and concentrated, then diluted with EtOAc. The organic layer was washed with saturated NaHCO3 (3×150 mL), H2O (2×250 mL), brine (1×250 mL) and dried over MgSO4. The crude product was purified by column chromatography using hex:EtOAc (4.5:0.5) as the eluant to give the title ester. Spectroscopic data: 1H NMR (300 MHz, CDCl3) δ 3.91 (s, 3H), 3.94 (s, 3H), 6.92 (d, J=8.79 Hz, 1H), 7.99 (dd, J=8.79 Hz, 1H), 8.24 (d, J=2.35 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557853B2
Source datasetuspto-grants-2013_10
ORD IDord-cb90c21ff234438dbb459dc727189e22
Source noteuspto-grants-2013_10