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HRID 127192作成日:2026年10月26日

Ethanol → 6-Methoxypyridine-3-carbaldehyde

https://huagongshe.com/reaction/127192

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Semicarbazide hydrochlorideHCID 11236—
反応物Sodium AcetateHCID 517045—
反応物2-Methoxy-5-pyridinecarbonitrileHCID 2736776—
触媒NickelHCID 935—
溶媒WaterHCID 962—
生成物6-Methoxypyridine-3-carbaldehydeHCID 336457650.3%

反応手順

A mixture of 2-methoxy-5-cyanopyridine (61.26 g), semi-carbazide hydrochloride (76.4 g), sodium acetate (74.92 g), ethanol (1,300 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 (1,000 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 (1,000 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 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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04255428
出典データセットuspto-grants-1981_03
ORD IDord-875292ae258549168306a618a2e45828
出典メモuspto-grants-1981_03