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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889707Generated: October 31, 2026

Methanol → Methyl 3-bromo-2-methoxybenzoate

https://huagongshe.com/reaction/1889707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Bromo-2-methoxybenzoic acidHCID 253598—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-bromo-2-methoxybenzoateHCID 4631108290%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Bromo-2-methoxybenzoic acid (2 g, 8.65 mmol, 1.0 eq) was dissolved in dry DCM and stirred for 10 minutes, cooled to 0° C. and slowly treated with oxalyl chloride (3.3 g, 25.9 mmol, 3 eq). Methanol in pyridine was added dropwise and the reaction mixture was stirred at ambient temperature. The solvents were evaporated under reduced pressure and the reaction mass was diluted with water. The aqueous mixture was extracted with ethyl acetate. The organic layer was dried with anhydrous Na2SO4 and concentrated under vacuum to afford the desired product (1.9 g, 90%). 1H NMR (400 MHz, CDCl3) δ 3.93 (s, 6H), 7.02-6.06 (t, 1H), 7.72-7.76 (m, 2H). MS (ESI): 247.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-a6554cb1f3c542b18c5d0618c7683390
Source noteuspto-grants-2013_08