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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749485Generated: October 26, 2026

Triethylamine → Ethyl 2-[2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoyl]-3-dimethylaminoacrylate

https://huagongshe.com/reaction/749485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantEthyl 3-(N,N-dimethylamino)acrylateHCID 121015—
Reactant2,4-Dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoic acidHCID 68798267—
SolventTolueneHCID 1140—
ProductEthyl 2-[2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoyl]-3-dimethylaminoacrylateHCID 6879620623.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

95 mg (0.27 mmol) of 2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoic acid were boiled with 0.98 ml of thionyl chloride under reflux for 3 hours. The thionyl chloride was distilled off, and the residue was mixed with 3 ml of toluene and concentrated in vacuo. The residue was taken up in 2 ml of toluene and added to a solution of 39 mg (0.27 mmol) of ethyl 3-dimethylaminoacrylate, 6 μl of triethylamine and 1 ml of toluene. The mixture was heated at 90° C. for 3 hours. The mixture was concentrated and chromatographed on silica gel (heptane:ethyl acetate=75:25 to 0:100 in 45 minutes). 30 mg (23%) of the desired product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402674B2
Source datasetuspto-grants-2008_07
ORD IDord-f63dff0bbe204ed5aa229156fe2f37ea
Source noteuspto-grants-2008_07