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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894649Generated: October 29, 2026

2-Chlorobenzaldehyde → HCID 54101000, compound

https://huagongshe.com/reaction/894649

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantEthyl 4,4-diethoxy-3-oxobutanoateHCID 11138577—
CatalystPiperidineHCID 8082—
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 eluant (benzene:ethyl acetate=10:1) to give pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284634
Source datasetuspto-grants-1981_08
ORD IDord-cc65c8c591504f1ca60444abbd8e3692
Source noteuspto-grants-1981_08