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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42468생성일: 2026년 10월 24일

Hydrochloric Acid → 4-Ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile

https://huagongshe.com/ko/reaction/42468

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물OxygenHCID 977—
반응물CyanoacetamideHCID 7898—
반응물Hexen-2-alHCID 12990—
반응물Potassium tert-butoxideHCID 23665647—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물4-Ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrileHCID 1564180031.7%

반응 단계

To a stirred solution of t-BuOK (22.85 g, 204.08 mmol) and cyanoacetamide (18.8 g, 224.1 mmol) in DMSO (300 mL) was added hex-3-en-2-one (20 g, 204.08 mmol) under argon atmosphere at room temperature. The reaction mixture was then stirred at room temperature for 30 min and then added additional t-BuOK (68.5 g, 612.05 mmol) was added. Argon gas was displaced by oxygen gas and the mixture stirred for 48 hrs at room temperature in presence of oxygen. Reaction was monitored by TLC. The reaction mixture was cooled to 0° C. and diluted with water (100 mL) followed by 4 N HCl (120 mL). The mixture was stirred for 15 min and the resulting solid was filtered. The solid was washed with water (1 L) and dried to afford the title compound, 4-ethyl-1,2-dihydro-6-methyl-2-oxopyridine-3-carbonitrile (10.5 g, 31%), as an off white solid. 1H NMR (CDCl3, 400 MHz): δ ppm 1.148-1.185 (t, 3H, J=7.4 Hz), 2.237 (s, 3H), 2.557-2.614 (m, 2H), 6.211 (s, 1H), 12.330 (broad s, 1H). MS (ES) [M+H]+ 161.06.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536179B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5337bd3dbb4b4fc08f61043b4f31a815
출처 메모uspto-grants-2013_09