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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127202생성일: 2026년 10월 26일

Ethanol → 2-Methoxypyridine-4-carbaldehyde

https://huagongshe.com/reaction/127202

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Semicarbazide hydrochlorideHCID 11236—
반응물Sodium AcetateHCID 517045—
반응물2-MethoxyisonicotinonitrileHCID 7204887—
촉매NickelHCID 935—
용매WaterHCID 962—
생성물2-Methoxypyridine-4-carbaldehydeHCID 276299635.1%

반응 단계

A mixture of 2-methoxy-4-cyanopyridine (57.2 g), semicarbazide hydrochloride (71.24 g), sodium acetate (69.86 g), ethanol (1,200 ml) and water (370 ml) was hydrogenated at 344 kPa using Raney nickel catalyst (1.0 g). The mixture was evaporated to a volume of 450 ml, water (900 ml) was added and the mixture was allowed to stand at 0° overnight. The mixture was filtered and the solid was washed with water and was dissolved in 10% hydrochloric acid (950 ml). Formaldehyde solution (36% w/v, 420 ml) was added and the mixture was warmed for 30 minutes, allowed to cool and was added to a solution of sodium acetate (280 g) in water (840 ml). The mixture was extracted with ether (3×500 ml) and the combined extracts were successively washed with aqueous potassium carbonate and water and were dried out evaporated to give 2-methoxypyridine-4-carboxaldehyde (20.53 g, 35%) m.p. 33-5° . A sample recrystallised from petroleum ether had m.p. 33-36°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04255428
출처 데이터셋uspto-grants-1981_03
ORD IDord-edd80c40248c4c72b02bb6f350d6e1c4
출처 메모uspto-grants-1981_03