HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255953Generated: October 30, 2026
Triethylamine → Ethyl 3-dimethylamino-2-(2,4-dichloro-5-fluorobenzoyl)acrylate
https://huagongshe.com/reaction/255953
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 3-(N,N-dimethylamino)acrylate | HCID 121015 | — |
| Reactant | 2,4-Dichloro-5-fluorobenzoyl chloride | HCID 2736821 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 3-dimethylamino-2-(2,4-dichloro-5-fluorobenzoyl)acrylate | HCID 53763646 | 83.3% |
Reaction Steps
14.3 g of ethyl 3-dimethylaminoacrylate and 10.5 g of triethylamine are added dropwise to a solution of 22.75 g of 2,4-dichloro-5-fluorobenzoyl chloride in 100 ml of anhydrous dioxane at 10° to 20° C., with stirring. The mixture is stirred at room temperature for 3 hours, heated at 40°-50° C. for 1 hour, and the solvent is removed by distillation in vacuo and the residue is taken up in methylene chloride/H2O. The phases are separated, and the aqueous solution is again extracted with methylene chloride. The CH2Cl2 solution is washed with water, dried with sodium sulphate, and the solvent is removed in vacuo. The crystalline residue is recrystallized from cyclohexane/light petroleum. 27.8 g of ethyl 3-dimethylamino-2-(2,4-dichloro-5-fluorobenzoyl)acrylate of melting point 94°-95° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04699992 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-ff1efb9d82af45a6a07d4ff1ecd9414a |
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| Source note | uspto-grants-1987_10 |
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