Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746238Generated: October 31, 2026

Benzene → 2-(4-Benzhydryl-1-piperazinyl)ethyl 2-(3-nitrobenzylidene)acetoacetate

https://huagongshe.com/reaction/746238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant3-NitrobenzaldehydeHCID 7449—
ReactantPiperidineHCID 8082—
ReactantButanoic acid, 3-oxo-, 2-[4-(diphenylmethyl)-1-piperazinyl]ethyl esterHCID 11740518—
SolventWaterHCID 962—
Product2-(4-Benzhydryl-1-piperazinyl)ethyl 2-(3-nitrobenzylidene)acetoacetateHCID 54110130—

Reaction Steps

A mixture of m-nitrobenzaldehyde (1.67 g), 2-(4-benzhydryl-1-piperazinyl)ethyl acetoacetate (4.20 g), benzene (40 ml) and piperidine (0.05 g) was refluxed for 4 hours, during which time the water produced was removed using a Dean-Stark trap. The mixture was washed with water and dried (MgSO4). The solvent was then distilled off and the residue was purified by column chromatography on silica gel (100 g) [eluent: ethyl ether-ethyl acetate (10:1, v/v)] to give 2-(4-benzhydryl-1-piperazinyl)ethyl 2-(3-nitrobenzylidene)acetoacetate as an oil. Yield 4.37 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04603135
Source datasetuspto-grants-1986_07
ORD IDord-8211de46831d460cb83280e10268f9b7
Source noteuspto-grants-1986_07