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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759042Generated: October 30, 2026

2-Chlorobenzaldehyde → HCID 54101000, compound

https://huagongshe.com/reaction/1759042

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 numberUS04338322
Source datasetuspto-grants-1982_07
ORD IDord-44cda513aada4362b4197649ce7bbc4c
Source noteuspto-grants-1982_07