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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973788Generated: October 30, 2026

Triethylamine → 2-(2,4-Difluoroanilino)-4,5-difluorobenzoic acid

https://huagongshe.com/reaction/973788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-DifluoroanilineHCID 9709—
Reactant2-Chloro-4,5-difluorobenzoic acidHCID 737171—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
Product2-(2,4-Difluoroanilino)-4,5-difluorobenzoic acidHCID 1499747563.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

A suspension of triethyl amine (15 ml, 0.11 mol), 2, 4-difluoroaniline (25 ml, 0.24 mol), copper bronze (2.7 g., 0.04 mol), in hot DMF (25 ml) was treated with a solution of 2-chloro-4,5-difluorobenzoic acid (23 g., 0.12 mol) in 25 ml of DMF and the temperature was maintained at 85° C. for 8 hours. The reaction mixture was allowed to cool to room temperature and was then stirred overnight. The reaction mixture was evaporated in vacuo and the residue was partitioned between ether and aqueous ammonium chloride. The organic phase was washed with 2N HCl and saturated aqueous lithium chloride solution. The ether was dried over sodium sulfate, treated with darco and then filtered and evaporated. The residue was crystallized from hexane-ether to afford 21.6 g (62%) of 2-(2,4-difluorophenylamino)-4,5-difluorobenzoic acid; m.p.: 215°-216° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05064958
Source datasetuspto-grants-1991_11
ORD IDord-ff785fd0d63b490992f893eb0cd5360c
Source noteuspto-grants-1991_11