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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918196Generated: October 31, 2026

2-Chlorobenzoic Acid → HCID 12226008, compound

https://huagongshe.com/reaction/918196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzoic AcidHCID 8374—
Reactant4-FluoroanilineHCID 9731—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassiumHCID 5462222—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
ProductHCID 12226008HCID 12226008—

Reaction Steps

The potassium salt of o-chlorobenzoic acid (25 g), 25 g. of 4-fluoroaniline, 9 g. potassium carbonate and 2 g. of copper powder were heated under reflux in 200 ml. dimethylformamide. After cooling the solvent was evaporated, the residue dissolved in 500 ml. of absolute ethanol, the solution was filtered and the filtrate evaporated. The residue was suspended in 300 ml. of methylene chloride and filtered. The solid (on 10 filter) was dissolved in 100 ml. of water and 45 g. of potassium carbonate was added. To this solution 65 ml. phosgene (12.5% in benzene) was added under vigorous stirring. The stirring was continued for 18 hours at room temperature. The precipitate, which had formed, was filtered off and washed with water. After air drying the filter case was dissolved in chloroform (200 ml.) and the solution treated with solid sodium carbonate, aluminium oxide and activated charcoal. The solvent was then exchanged for ether and the material, which crystallized, was collected by filtration, m.p. 199°-201°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03969506
Source datasetuspto-grants-1976_07
ORD IDord-0534e3a718dc4bfeb47be098a54f4919
Source noteuspto-grants-1976_07