Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415918Generated: October 27, 2026

Benzenamine, 2-chloro-4-fluoro- → HCID 178471927, compound

https://huagongshe.com/reaction/1415918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 2-chloro-4-fluoro-HCID 75013—
ReactantEthyl 3-(2,4,5-trifluorophenyl)-3-oxo-2-(ethoxymethylene)propanoateHCID 54008204—
SolventChloroformHCID 6212—
ProductHCID 178471927HCID 178471927—

Reaction Steps

With ice cooling, 5 ml of a chloroform solution containing 1.2 ml of 2-chloro-4-fluoroaniline was added dropwise to 13 ml of a chloroform solution containing 2.46 g of ethyl 2-(2,4,5-trifluorobenzoyl)-3-ethoxyacrylate and stirred overnight at room temperature. The solvent was distilled off then to the residue, ethanol was added. The resulting crystals were collected by filtration and washed with diethyl ether, to give ethyl 2-(2,4,5-trifluorobenzoyl)-3-(2-chloro-4-fluorophenylamino)acrylate. To 15 ml of a N,N-dimethylformamide solution containing 3.00 g of ethyl 2-(2,4,5-trifluorobenzoyl)-3-(2-chloro-4-fluorophenylamino)acrylate was added 1.03 g of potassium carbonate. The solution was stirred for 90 minutes at room temperature. The reaction solution was poured into ice water, the precipitated solid was collected by filtration and washed with ethanol and diethyl ether, to give 2.74 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05910498
Source datasetuspto-grants-1999_06
ORD IDord-52787acfb65f48819a1e3b50186df657
Source noteuspto-grants-1999_06