돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1250244생성일: 2026년 10월 25일

Triethylamine → (E)-N-Methyl-N-[4-(3-aminophenyl)-3-buten-1-yl]benzamide

https://huagongshe.com/reaction/1250244

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-IodoanilineHCID 12271—
반응물N-Methyl-N-(3-buten-1-yl)benzamideHCID 10559557—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물(E)-N-Methyl-N-[4-(3-aminophenyl)-3-buten-1-yl]benzamideHCID 15549897112.7%

반응 조건

온도107.5 °C

반응 단계

Under a nitrogen atmosphere, a mixture of N-methyl-N-(3-buten-1-yl)benzamide (2.15 g, 11.36 mmol), 3-iodoaniline (2.49 g, 11.36 mmol, Aldrich Chemical Company), palladium(II) acetate (25.5 mg, 0.11 mmol), and triethylamine (2.30 g, 22.70 mmol) was stirred and heated under reflux at 105-110° C. (oil bath temperature) for 52 h. The dark-brown solution was allowed to cool to ambient temperature and was diluted with water (20 mL) and CHCl3 (40 mL). The water layer was separated and extracted with CHCl3 (2×10 mL). The combined CHCl3 extracts were washed with saturated NaCl solution (10 mL), dried (CHCl3), filtered, and concentrated by rotary evaporation. Further drying under high vacuum (0.3 mm Hg) for 15 h produced a viscous, brown oil (3.59 g). The crude material was purified by column chromatography on silica gel (155.5 g, 4.0 cm i.d.×60.5 cm column) eluting with EtOAc (25→67%, v/v) in CHCl3. Fractions containing the product (Rf 0.34 in EtOAc-CHCl3, 1:1, v/v) were combined, concentrated by rotary evaporation, and vacuum dried at 45° C. for 15 h to give 1.60 g (50.2%) of an amber oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06337351B1
출처 데이터셋uspto-grants-2002_01
ORD IDord-b4c3173b21b04f4bbb0254ef333b748b
출처 메모uspto-grants-2002_01