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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166140Generated: November 2, 2026

Oxalyl chloride → Quinoline-3-carbonyl Chloride

https://huagongshe.com/reaction/1166140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantQuinoline-3-carboxylic acidHCID 80971—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductQuinoline-3-carbonyl ChlorideHCID 11030631—

Reaction Steps

To a suspension of 3-quinolinecarboxylic acid (580 mg, 3.35 mmol) in dichloromethane (25 mL) was added oxalyl chloride (2M in CH2Cl2, 3.4 mL, 6.7 mmol) dropwise at room temperature. DMF (1 drop) was added, resulting in immediate gas formation. The reaction mixture was stirred at room temperature for 2 h. Dichloromethane was evaporated. Additional dichloromethane (20 mL) was added to the residue. Concentration of the organic solvent gave the crude product. (640 mg, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613747B2
Source datasetuspto-grants-2003_09
ORD IDord-cf4121c1fd5540f6baa7d4341bdba3b1
Source noteuspto-grants-2003_09