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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4582생성일: 2026년 10월 25일

Ethanol → 2-(4-Acetylaminophenoxy)ethyl 2,6-dimethyl-5-(2-ethylthioethoxycarbonyl)-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/4582

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물2-(4-Acetylaminophenoxy)ethyl 2-(3-nitrobenzylidene)acetylacetateHCID 57315737—
반응물2-Ethylthioethyl 3-aminocrotonateHCID 86741408—
생성물2-(4-Acetylaminophenoxy)ethyl 2,6-dimethyl-5-(2-ethylthioethoxycarbonyl)-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylateHCID 2015126460%

반응 조건

온도-5 °C

반응 단계

15 g (0.04 moles) of 2-(4-acetylaminophenoxy)ethyl 2-(3-nitrobenzylidene)acetylacetate and 6.88 g (0.04 moles) of 2-ethylthioethyl 3-aminocrotonate were heated under reflux in 35 ml of ethanol for 8 hours. The solution was then cooled to -5° C. to obtain 2-(4-acetylaminophenoxy)ethyl 2,6-dimethyl-5-(2-ethylthioethoxycarbonyl)-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate as a yellow powder melting--after recrystallisation in ethanol--at 100°-104° C. The yield is 60% of the theoretical yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727066
출처 데이터셋uspto-grants-1988_02
ORD IDord-0762afb0cbd843a58951b15e1705bb6e
출처 메모uspto-grants-1988_02