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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164575Generated: October 29, 2026

2-Chlorobenzaldehyde → HCID 54101000, compound

https://huagongshe.com/reaction/1164575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantPiperidineHCID 8082—
ReactantEthyl 4,4-diethoxy-3-oxobutanoateHCID 11138577—
SolventBenzeneHCID 241—
ProductHCID 54101000HCID 54101000106.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04370334
Source datasetuspto-grants-1983_01
ORD IDord-7d1028e00151403c974405e7e6640ff2
Source noteuspto-grants-1983_01