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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 224880생성일: 2026년 10월 23일

Ethanol → 6-Methoxypyridine-3-carbaldehyde

https://huagongshe.com/ko/reaction/224880

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Semicarbazide hydrochlorideHCID 11236—
반응물Sodium AcetateHCID 517045—
반응물2-Methoxy-5-pyridinecarbonitrileHCID 2736776—
촉매NickelHCID 935—
용매WaterHCID 962—
생성물6-Methoxypyridine-3-carbaldehydeHCID 336457650.3%

반응 단계

A mixture of 2-methoxy-5-cyanopyridine (61.26 g), semicarbazide hydrochloride (76.4 g), sodium acetate (74.92 g), ethanol (1300 ml) and water (400 ml) was hydrogenated at 344 kPa using Raney nickel catalyst (1.0 g). The mixture was evaporated to a volume of 500 ml, water (1000 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 dissolved in 10% hydrochloric acid (1000 ml). Formaldehyde solution (36% w/v, 450 ml) was added and the mixture was warmed for 15 minutes, allowed to cool and was added to a solution of sodium acetate (298.5 g) in water (900 ml). This mixture was extracted with ether (3×500 ml) and the combined extracts were successively washed with aqueous potassium carbonate and water and were dried and evaporated to give 6-methoxypyridine-3-carboxaldehyde (31.5 g, 50%) m.p. 48°-49°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04234588
출처 데이터셋uspto-grants-1980_11
ORD IDord-c2900c37ae4746098799c15968b2f5e7
출처 메모uspto-grants-1980_11