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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600878Generated: October 31, 2026

Piperidine → 3-(4-methoxybenzylidene)-oxindole

https://huagongshe.com/reaction/1600878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantOxindoleHCID 321710—
SolventEthanolHCID 702—
Product3-(4-methoxybenzylidene)-oxindoleHCID 280310971%

Reaction Steps

2.0 g of oxindole was dissolved in 40 ml of ethanol, and 2.0 g of p-anisaldehyde was added thereto at room temperature. Subsequently, 1.5 ml of piperidine was added, and the mixture was refluxed with heat for 13 hours. After completion of reaction, the reaction mixture was cooled. Crystals that precipitated were collected by filtration. The resultant crude product was washed with methanol, to thereby obtain 2.6 g (yield 71%) of the title compound in the form of yellow crystals. The melting point and elementary analysis data are shown in Table 13, and NMR and MS spectrum data are shown in Table 14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977130
Source datasetuspto-grants-1999_11
ORD IDord-7bb46894e1654296b284ecce26c6fed7
Source noteuspto-grants-1999_11