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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248664Generated: October 29, 2026

2-Chlorobenzaldehyde → HCID 54101000, compound

https://huagongshe.com/reaction/1248664

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 eluent (benzene:ethyl acetate=10:1) to give pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04525478
Source datasetuspto-grants-1985_06
ORD IDord-cee4a651c5074a0caff999a85883590b
Source noteuspto-grants-1985_06