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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870951Generated: October 30, 2026

Benzene → 4-Hydroxy-6-methyl-3-(4-nitrophenyl)acryloyl-2-pyrone

https://huagongshe.com/reaction/1870951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant4-NitrobenzaldehydeHCID 541—
ReactantPiperidineHCID 8082—
ReactantDehydroacetic acidHCID 122903—
SolventWaterHCID 962—
Product4-Hydroxy-6-methyl-3-(4-nitrophenyl)acryloyl-2-pyroneHCID 13540605982%

Reaction Steps

4-Nitrobenzaldehyde (4.5 g, 29.7 mmol) and then a number of drops of piperidine were added to a benzene (40 ml) solution of dehydroacetic acid (5.00 g, 29.7 mmol) at room temperature, after which refluxing was performed for 6 hours while eliminating water by azeotropy. The majority of the benzene was distilled of directly, and then the distillation taken to dryness under reduced pressure. Following which, when recrystallization was performed from ethanol, 4-hydroxy-6-methyl-3-(4-nitrophenyl)acryloyl-2-pyrone (7.3 g, 82%) was obtained as orange crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06100292
Source datasetuspto-grants-2000_08
ORD IDord-bdada907a2d44d15be6a7dc8e5a6fd8f
Source noteuspto-grants-2000_08