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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859077Generated: October 25, 2026

Benzaldehyde → 2-Benzylidene-1,3-indandione

https://huagongshe.com/reaction/1859077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant1,3-IndandioneHCID 11815—
CatalystPiperidineHCID 8082—
SolventBenzeneHCID 241—
Product2-Benzylidene-1,3-indandioneHCID 23782272.1%

Reaction Steps

To a solution of 1,3-indandione (43.8 g) and piperidine (44 mg) in dry benzene (500 ml) was added benzaldhyde (31.8 g). The mixture was heated to reflux and the water generated was removed by Dean-Stark trap. After 24 hours, the mixture was evaporated to dryness. The residue was recrystallized from ethanol (200 ml) to give 2-benzylidene-1,3-indandione as a yellow solid (50.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153645
Source datasetuspto-grants-2000_11
ORD IDord-4cdc2d56b9d643e9bb22b4106b8ec394
Source noteuspto-grants-2000_11