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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614581Generated: October 29, 2026

2-Chlorobenzaldehyde → HCID 54101000, compound

https://huagongshe.com/reaction/614581

Reaction equation

Participants

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

Reaction Steps

(2)-(1) A solution of 2-chlorobenzaldehyde (14.0570 g), ethyl 4,4-diethoxyacetoacetate (21.8240g) and piperidine (1 ml) in benzene (100 ml) was refluxed under azeotropic dehydration for 4 hours. The resultant solution was washed with water, dried and concentrated to give oily ethyl 2-(2-chlorobenzylidene)-4,4-diethoxyacetoacetate. The mixture of the compound obtained above and ethyl 3aminocrotonate (12.92 g) was heated in an oil bath (about 100° C.) for 8 hours. The reaction mixture was dissolved in ethyl acetate, washed with water, dried and then the solvent was removed to give crude oil (52.4 g). The oil was purified by column chromatography on silica gel with an eluent (benzene:ethyl acetate = 20:1) to give diethyl 2-methyl-4-(2-chlorophenyl)-6-diethoxymethyl-1.4-dihydropyridine-3,5-dicarboxylate, which was recrystallized from n-hexane to give the pure crystals (20.2445 g), m.p. 75° to 77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04145432
Source datasetuspto-grants-1979_03
ORD IDord-93f4f15eda8d401190ab2baa5c7081ed
Source noteuspto-grants-1979_03