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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700338Generated: October 26, 2026

Triethylamine → N-methyl-3-oxo-N-(3-phenyl-2-propene-1-yl)butyramide

https://huagongshe.com/reaction/1700338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiketeneHCID 12661—
ReactantN-methyl-3-phenylprop-2-en-1-amineHCID 189183—
ReactantSodium BicarbonateHCID 516892—
SolventTolueneHCID 1140—
ProductN-methyl-3-oxo-N-(3-phenyl-2-propene-1-yl)butyramideHCID 53834343—

Reaction Steps

0.736 g (5.0 mmol) of methyl-(3-phenyl-2-propene-1-yl)amine, 0.386 ml (5.0 mmol) of ketene dimer and 0.07 ml (0.50 mmol) of triethylamine were heated at 70° C. under stirring in 5 ml of toluene overnight. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture. After the extraction with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by the thin-layer silica gel chromatography (ethyl acetate) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350762B1
Source datasetuspto-grants-2002_02
ORD IDord-017d1d1bc74d449d88a6fc94e654953c
Source noteuspto-grants-2002_02