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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174900Generated: October 31, 2026

Oxalyl chloride → Methyl 2-bromothiophene-3-carboxylate

https://huagongshe.com/reaction/2174900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Bromo-3-thiophenecarboxylic acidHCID 12320971—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-bromothiophene-3-carboxylateHCID 5330219698.1%

Reaction Steps

2-bromo-3-thiophene carboxylic acid (1.0 eq, 12.56 g, 60.66 mmol) was suspended in CH2Cl2 (200 ml). Oxalyl chloride (1.1 eq, 5.9 ml, 67.16 mmol) and 5 drops of DMF were added, inducing formation of gas. The mixture was stirred overnight at room temperature and the volatiles were removed in vacuo. The resulting solid was suspended in dry methanol (150 ml) and the mixture heated to ebullition. Evaporation of the solvents afforded methyl 2-bromo-3-thiophene carboxylate (13.16 g, 98% yield) as a crude brown oil. LCMS (ES): 99% pure, m/z not detected;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062043B2
Source datasetuspto-grants-2015_06
ORD IDord-e803f10a458f4a3c8082b631735d402d
Source noteuspto-grants-2015_06