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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 3,4-dichlorophenylacetate | HCID 2737422 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | M-Xylene | HCID 7929 | — |
| Product | Ethyl 2-(3,4-dichlorophenyl)acrylate | HCID 68871722 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470816B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-11372bb424614079a4c3aaf91b641a85 |
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| Source note | uspto-grants-2013_06 |
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