HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164575Generated: October 29, 2026
2-Chlorobenzaldehyde → HCID 54101000, compound
https://huagongshe.com/reaction/1164575
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Ethyl 4,4-diethoxy-3-oxobutanoate | HCID 11138577 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54101000 | HCID 54101000 | 106.4% |
Reaction Steps
A solution of 2-chlorobenzaldehyde (1.0543 g), ethyl 4,4-diethoxyacetoacetate (1.6477 g) and piperidine (1 to 2 drop(s) in benzene (30 ml) was refluxed under azeotropic dehydration for 4.5 hours. After cooling, the resultant solution was washed with water and dried. The solvent was removed from the solution to give orange oil (2.7196 g) of ethyl 2-(2-chlorobenzylidene)-4,4-diethoxyacetoacetate. The mixture of the compound obtained above and ethyl 3-amino-4,4-diethoxycrotonate (1.6580 g) was heated with stirring at about 100° C. for 1.5 hours and about 120° C. for 8 hours. After cooling, the reaction mixture was dissolved in ethyl acetate. The solution was washed with water and dried, and then the solvent was removed from the solution to give orange oil (4.21 g) of diethyl 2,6-bis(diethoxymethyl)-4-(2-chlorophenyl)-1,4-dihydropyridine-3,5-dicarboxylate. The product was purified by a column chromatography on silica gel with an eluent (benzene: ethyl acetate=10:1) to give pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04370334 |
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| Source dataset | uspto-grants-1983_01 |
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| ORD ID | ord-7d1028e00151403c974405e7e6640ff2 |
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| Source note | uspto-grants-1983_01 |
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