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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255959Generated: October 26, 2026

Triethylamine → Ethyl 3-diethylamino-2-(2,4-dichloro-5-fluorobenzoyl)acrylate

https://huagongshe.com/reaction/255959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 3-(diethylamino)acrylateHCID 139639—
Reactant2,4-Dichloro-5-fluorobenzoyl chlorideHCID 2736821—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 3-diethylamino-2-(2,4-dichloro-5-fluorobenzoyl)acrylateHCID 5414810380.2%

Reaction Steps

First 17.1 g of ethyl 3-diethylaminoacrylate are added dropwise and then 10.5 g of triethylamine are added to a solution of 22.75 g of 2,4-dichloro-5-fluorobenzoyl chloride in 80 ml of anhydrous dioxane, while cooling in ice and stirring. The mixture is stirred at room temperature for one hour, heated to boiling under reflux for 45 minutes, and the solvent is removed by distillation in vacuo, and the oily residue is taken up in methylene chloride/water. The phases are separated, and the aqueous solution is again extracted with methylene chloride. The combined organic phases are washed with water, dried with sodium sulphate, and the methylene chloride is removed in vacuo. 29 g of ethyl 3-diethylamino-2-(2,4-dichloro-5-fluorobenzoyl)acrylate are obtained as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699992
Source datasetuspto-grants-1987_10
ORD IDord-3d3b491826424629a8c5a2f225a8892a
Source noteuspto-grants-1987_10