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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217436Generated: October 29, 2026

Methanol → Methyl 4-bromo-5-ethylthiophene-2-carboxylate

https://huagongshe.com/reaction/217436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant4-Bromo-5-ethylthiophene-2-carboxylic acidHCID 3766372—
ProductMethyl 4-bromo-5-ethylthiophene-2-carboxylateHCID 57826917—

Reaction Conditions

Temperature0 °C

Reaction Steps

The suspension of 4-bromo-5-ethylthiophene-2-carboxylic acid (800 mg) in MeOH (4 mL) was added dropwise SOCl2 (0.50 mL) at 0° C. The reaction mixture was stirred at 0° C. for 1 hour, warmed to 60° C., and then stirred for 15 hours. The reaction liquid was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (automatic purification device, hexane:EtOAc=98:2 to 70:30) to obtain methyl 4-bromo-5-ethylthiophene-2-carboxylate (765.0 mg) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193378B2
Source datasetuspto-grants-2012_06
ORD IDord-22af2f5622c6457db064bd64a56613b4
Source noteuspto-grants-2012_06