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HRID 1032991생성일: 2026년 10월 25일

Cyanoacetamide → 5-Ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile

https://huagongshe.com/reaction/1032991

반응식

참여 물질

역할이름HCID투입량
반응물CyanoacetamideHCID 7898—
반응물Piperidinium acetateHCID 3014295—
반응물SodiumHCID 5360545—
반응물2-Ethyl-3-oxobutanalHCID 15228410—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물5-Ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrileHCID 10241109—

반응 단계

According to the method described in J.Heterocyclic Chem., 24, 351 (1987), a mixture of 2-ethyl-3-oxobutanal, sodium salt (37.5 g, 0.275 mmol), cyanoacetamide (25.2 g, 0.30 mol), aqueous piperidinium acetate (22 mL) [prepared from glacial acetic acid (4.2 mL), water (10 mL) and piperidine (7.2 mL)] in water (775 ml) was refluxed for four hours. Glacial acetic acid (30 ml) was added cautiously (much foaming) as the product precipitated. Upon cooling to room temperature, the product was collected by filtration, washed with cold water and air dried to yield 22.3 g (50%), m.p. 237°-240° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05308854
출처 데이터셋uspto-grants-1994_05
ORD IDord-e5332a0361704a359350e8b844c198cc
출처 메모uspto-grants-1994_05