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HRID 1700338作成日:2026年10月27日

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

https://huagongshe.com/reaction/1700338

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物DiketeneHCID 12661—
反応物N-methyl-3-phenylprop-2-en-1-amineHCID 189183—
反応物Sodium BicarbonateHCID 516892—
溶媒TolueneHCID 1140—
生成物N-methyl-3-oxo-N-(3-phenyl-2-propene-1-yl)butyramideHCID 53834343—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06350762B1
出典データセットuspto-grants-2002_02
ORD IDord-017d1d1bc74d449d88a6fc94e654953c
出典メモuspto-grants-2002_02