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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1178192생성일: 2026년 10월 27일

Triethylamine → Ethyl 2-(E-2-(4-(N,N-dimethylaminomethyl)phenyl)ethen-1-yl)nicotinate

https://huagongshe.com/reaction/1178192

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Tri-o-tolylphosphineHCID 80271—
반응물Benzenemethanamine, ar-ethenyl-N,N-dimethyl-HCID 519956—
반응물Ethyl chloronicotinateHCID 2796614—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Ethyl 2-(E-2-(4-(N,N-dimethylaminomethyl)phenyl)ethen-1-yl)nicotinateHCID 1181105933.9%

반응 조건

온도140 °C

반응 단계

6.7 g (39 mmol) of ethyl 2-chloronicotinate, 8.2 g (51 mmol) of 4-(N,N-dimethylaminomethyl)styrene, 9.9 g (98 mmol) of triethylamine, 0.36 g of palladium(II) acetate and 0.96 [lacuna] of tri(o-tolyl)phosphine were mixed in 150 ml of dimethylformamide and, after addition of 1 ml of water, stirred at 140° C. for 13 h. The reaction mixture was then concentrated in vacuo, and the resulting residue was partitioned between ethyl acetate and water. The organic phase was separated off, washed with water, dried and concentrated in vacuo. The residue was then crystallized as oxalate from isopropanol after addition of an equivalent amount of oxalic acid. 4.1 g (27%) of the product were obtained as monooxalate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07276500B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-7cb28733a5ff47dbacee37355451ca60
출처 메모uspto-grants-2007_10