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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888991Generated: November 3, 2026

Oxalyl chloride → HCID 86666737, compound

https://huagongshe.com/reaction/1888991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2,3-Dichloro-4-fluorobenzoic acidHCID 10330705—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 86666737HCID 86666737100%

Reaction Steps

2,3-dichloro-4-fluorobenzoic acid (I32) (5.76 g, 27.6 mmol) was suspended in dichloromethane (DCM) (150 mL) at 0° C. and treated with oxalyl chloride (2.89 mL, 33.1 mmol). The mixture was stirred at 0° C. for 10 minutes before 5 drops of DMF were added. The mixture was stirred to room temperature over 4 h. Solvents were removed in vacuo and the residue was azeotroped with toluene (3×100 mL). The residue was used directly in subsequent steps without further purification, assuming 100% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501946B2
Source datasetuspto-grants-2013_08
ORD IDord-e095f388132b4e5b8f9c587a9cdc0c8c
Source noteuspto-grants-2013_08