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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41634Generated: October 29, 2026

Methanol → Methyl 2-bromofuran-3-carboxylate

https://huagongshe.com/reaction/41634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Bromofuran-3-carboxylic acidHCID 21162497—
ProductMethyl 2-bromofuran-3-carboxylateHCID 10845885—

Reaction Steps

2-Bromofuran-3-carboxylic acid (5.0 g, 26 mmol, 1 eq.) was dissolved in MeOH (100 mL) and the mixture was degassed and purged with nitrogen (2×). SO2Cl2 (15 mL, 0.2 mol, 7.7 eq.) was added dropwise and the resulting mixture was stirred for two days at room temperature. The mixture was then concentrated and DCM (150 mL) was added. Saturated NaHCO3 (20 mL) was added, and the resulting mixture was stirred at room temperature for 15 minutes. The organic layer was washed with saturated NaHCO3 (20 mL), water (20 mL), and saturated aqueous NaCl (20 mL), then dried over Na2SO4, filtered and concentrated to yield 2-bromofuran-3-carboxylic acid methyl ester (5.0 g) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530663B2
Source datasetuspto-grants-2013_09
ORD IDord-564aec7f2c784d2086d28579d62a7046
Source noteuspto-grants-2013_09