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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700331Generated: October 29, 2026

Water → 2-acetyl-3-(3-chlorophenyl)-N-(3-phenyl-2-propene-1-yl)acrylamide

https://huagongshe.com/reaction/1700331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPiperidineHCID 8082—
Reactant3-ChlorobenzaldehydeHCID 11477—
ReactantHCID 53935748HCID 53935748—
SolventBenzeneHCID 241—
Product2-acetyl-3-(3-chlorophenyl)-N-(3-phenyl-2-propene-1-yl)acrylamideHCID 54139120—

Reaction Steps

652 mg (3.00 mmol) of 3-oxo-N-(3-phenyl-2-propene-1-yl)butyramide, 0.340 ml (3.00 mmol) of 3-chlorobenzaldehyde and 0.030 ml (0.30 mmol) of piperidine were heated under reflux in 25 ml of benzene overnight while water was removed. Benzene was evaporated under reduced pressure. The residue was purified by the silica gel chromatography (hexane/ethyl acetate=2/1) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350762B1
Source datasetuspto-grants-2002_02
ORD IDord-c12809298a83489e8827c50a4fb0ee21
Source noteuspto-grants-2002_02