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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614583Generated: October 29, 2026

Water → HCID 54504306, compound

https://huagongshe.com/reaction/614583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPiperidineHCID 8082—
Reactant2-NitrobenzaldehydeHCID 11101—
ReactantEthyl 4,4-diethoxy-3-oxobutanoateHCID 11138577—
SolventBenzeneHCID 241—
ProductHCID 54504306HCID 54504306—

Reaction Steps

(4)-(1) A solution of 2-nitrobenzaldehyde (9.0672 g), ethyl 4,4-diethoxyacetoacetate (13.0944 g) and piperidine (1ml) in benzene (45 ml) was refluxed under azeotropic dehydration for 3 hours. To the resultant solution was added water, and the solution was extracted with diethyl ether. The extract was washed three times with water, dried and then the solvent was removed under reduced pressure to give ethyl 2-(2-nitrobenzylidene)-4,4-diethoxyacetoacetate. The mixture of the compound obtained above and ethyl 3-aminocrotonate (7.7496 g) was heated in an oil bath (95° to 100° C.) for 8 hours. The resultant mixture was extracted with diethyl ether, and the extract was washed with water and dried. The solvent was removed from the extract. The residue was purified by column chromatography on silica gel with an eluent (benzene : ethyl acetate = 20:1) to give oily diethyl 2-methyl-4-(2-nitrophenyl)-6-diethoxymethyl-1,4-dihydropyridine-3,5-dicarboxylate (19.3 g). The product was crystallized in n-hexane and the crystals were collected by filtration and then recrystallized from a mixture of n-hexane and diethyl ether to give the pure compound, m.p. 80° to 81.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04145432
Source datasetuspto-grants-1979_03
ORD IDord-5700eea27dea43b1a36d20f038fd1e6b
Source noteuspto-grants-1979_03