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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238276Generated: October 25, 2026

Methanol → Methyl 5-bromothiophene-3-carboxylate

https://huagongshe.com/reaction/238276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant5-Bromothiophene-3-carboxylic acidHCID 12039978—
ProductMethyl 5-bromothiophene-3-carboxylateHCID 45873035—

Reaction Steps

5-Bromo-thiophene-3-carboxylic acid (13 g, 64 mmol) was dissolved in methanol (140 mL). Concentrated sulphuric acid (6.5 mL) was added and the mixture heated at reflux for 14 hours. The reaction was quenched by adding a solution of saturated aqueous sodium bicarbonate and most of the solvent was removed by evaporation under vacuum. The mixture was then diluted with a solution of saturated aqueous sodium bicarbonate and the product extracted with DCM. The organic solution was dried over sodium sulphate, filtered and the solvent removed by evaporation to give a white crystalline solid (13.2 g). 1H NMR (400 MHz, CDCl3): δ 8.0 (s, 1H), 7.5 (s, 1H), 3.85 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642621B2
Source datasetuspto-grants-2014_02
ORD IDord-b9da8d2ffc3b4b689872ff25615d0d33
Source noteuspto-grants-2014_02