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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415390Generated: November 2, 2026

Oxalyl chloride → 5-Bromofuran-2-carbonyl chloride

https://huagongshe.com/reaction/2415390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant5-Bromo-2-furanecarboxylic acidHCID 68511—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product5-Bromofuran-2-carbonyl chlorideHCID 2757011—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 5-bromo-2-furoic acid (2.1 g, 6.856 mmol) in THF (20 mL) was added oxalyl chloride (0.66 mL, 7.541 mmol). 2 drops of DMF were then added to the reaction mixture, with bubbles of CO observed to come out vigorously. Oxalyl chloride ((COCl)2) (0.1 mL) was then added. The reaction mixture was stirred at room temperature for 10 min and at 90° C. for 10 min. Solvent and excess (COCl)2 were taken off under vacuum to yield 5-bromo-furan-2-carbonyl chloride as a pale yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818646B2
Source datasetuspto-grants-2004_11
ORD IDord-e02feec050234453bf06afed686a6cd0
Source noteuspto-grants-2004_11