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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970687Generated: October 30, 2026

Oxalyl chloride → 4-Cyano-2-fluorobenzoyl chloride

https://huagongshe.com/reaction/970687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4-Cyano-2-fluorobenzoic acidHCID 590659—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-Cyano-2-fluorobenzoyl chlorideHCID 22345343—

Reaction Steps

To a suspension of 4-cyano-2-fluoro benzoic acid (650 mg, 3.9 mmol) in CH2Cl2 (20 mL) were added 2 drops of DMF and oxalyl chloride (0.7 mL, 7.8 mmol). The mixture was stirred at rt overnight and became a clear solution. The volatile was evaporated to dryness to give 4-cyano-2-fluoro-bezoyl chloride. To a solution of compound 6 (900 mg, 2.62 mmol) in THF (10 mL) was added a THF solution of 4-cyano-2-fluoro-bezoyl chloride. The mixture was stirred for 1 h, and concentrated. The residue was dissolved in EtOAc, washed with sat NaHCO3 and water. The organic layer was dried and evaporated to give compound 7 (1.2 g, 94% yield). MS found for C25H20ClFN4O2Si as (M+H)+: 491.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312235B2
Source datasetuspto-grants-2007_12
ORD IDord-ac9618a0430942a59ff612f5e5a00bf4
Source noteuspto-grants-2007_12