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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164584Generated: October 28, 2026

Piperidine → Benzyl 2-[(2-nitrophenyl)methylidene]-3-oxobutanoate

https://huagongshe.com/reaction/1164584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant2-NitrobenzaldehydeHCID 11101—
ReactantBenzyl acetoacetateHCID 142266—
SolventBenzeneHCID 241—
ProductBenzyl 2-[(2-nitrophenyl)methylidene]-3-oxobutanoateHCID 54323135107.9%

Reaction Steps

A mixture of 2-nitrobenzaldehyde (3.023 g), benzyl acetoacetate (3.802 g) and piperidine (272.5 mg) in benzene (10 ml), was treated in a substantially similar manner that of Example 1-11) to give a brown oil (6.94 g) of benzyl 2-(2-nitrobenzylidene)acetoacetate, which was further treated with ethyl 3-amino-4,4-diethoxycrotonate (4.34 g) to give a dark brown oil (10.3 g). This oil was purified by column chromatography on silica-gel and the resultant oil (3.8 g) was crystallized to give crystals (1.65 g) of benzyl 2-methyl-4-(2-nitrophenyl)-5-ethoxycarbonyl-6-diethoxymethyl-1,4-dihydropyridine-3-carboxylate, m.p. 103° to 103.5° C. (recrystallized from a mixture of diisopropyl ether and n-hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04370334
Source datasetuspto-grants-1983_01
ORD IDord-8aeeee6144c54592b79652c9cf7587e4
Source noteuspto-grants-1983_01