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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260908Generated: October 25, 2026

Formaldehyde → Ethyl 2-(3,4-dichlorophenyl)acrylate

https://huagongshe.com/reaction/1260908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantDiethyl OxalateHCID 7268—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3,4-dichlorophenylacetateHCID 2737422—
SolventEthanolHCID 702—
SolventM-XyleneHCID 7929—
ProductEthyl 2-(3,4-dichlorophenyl)acrylateHCID 6887172271%

Reaction Steps

To a solution of sodium hydride (60% in oil, 6.56 g) in m-xylene (100 mL) was slowly added ethanol (15.7 mL) at 0° C. and then diethyl oxalate (32.0 g) was added. Furthermore, a solution of ethyl 3,4-dichlorophenylacetate (51.0 g) in m-xylene (30 mL) was added at 0° C., and the mixture was stirred at room temperature for 14 hr. To the reaction mixture was added 37% aqueous formalin solution (140 mL) at room temperature, and the mixture was stirred at room temperature for 1 hr. Furthermore, potassium carbonate (115 g) was added at room temperature, and the mixture was stirred at room temperature for 1 hr. The insoluble material was filtered off, and the filtrate was partitioned between ethyl acetate (500 mL) and water (500 mL). The organic layer was separated, washed with brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent; 5% ethyl acetate/hexane) to give crude ethyl 2-(3,4-dichlorophenyl)acrylate (38.1 g, 44%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470816B2
Source datasetuspto-grants-2013_06
ORD IDord-11372bb424614079a4c3aaf91b641a85
Source noteuspto-grants-2013_06