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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402776Generated: October 31, 2026

Benzaldehyde → Benzaldehyde

https://huagongshe.com/reaction/1402776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantPiperidineHCID 8082—
ReactantEthyl AcetoacetateHCID 8868—
ProductBenzaldehydeHCID 240—
ProductAcetoacetateHCID 6971017—

Reaction Steps

The mixture of benzaldehyde (21.22 g) and ethyl acetoacetate (52.06 g) was cooled in an ice bath. Piperidine (3.3 ml) was added with stirring. The resulting mixture was kept at rt for 3 days whereupon it solidifies. The solid was recrystallised from ethanol (100 ml) to give a light yellowish solid (the bis-adduct of acetoacetate to benzaldehyde). The powdered solid was added in portions to 50% NaOH (200 ml) with stirring. The resulting yellow slurry was diluted with ethanol (70 ml) and stirred at reflux for 2 h. After addition of ice water (100 ml) and cooling in an ice bath the mixture was acidified with conc. HCl to give a white precipitate. The solid was collected by suction filtration and washed with water. After drying in vacuo 3-phenylglutaric acid (16.4 g) was obtained as colourless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912186B2
Source datasetuspto-grants-2014_12
ORD IDord-0e178660abd34e9db8bd492b963b8192
Source noteuspto-grants-2014_12