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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1700338생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1700338

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DiketeneHCID 12661—
반응물N-methyl-3-phenylprop-2-en-1-amineHCID 189183—
반응물Sodium BicarbonateHCID 516892—
용매TolueneHCID 1140—
생성물N-methyl-3-oxo-N-(3-phenyl-2-propene-1-yl)butyramideHCID 53834343—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06350762B1
출처 데이터셋uspto-grants-2002_02
ORD IDord-017d1d1bc74d449d88a6fc94e654953c
출처 메모uspto-grants-2002_02