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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719155Generated: November 1, 2026

Ethanol → 2-Methoxypyridine-4-carbaldehyde

https://huagongshe.com/reaction/1719155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSemicarbazide hydrochlorideHCID 11236—
ReactantSodium AcetateHCID 517045—
Reactant2-MethoxyisonicotinonitrileHCID 7204887—
CatalystNickelHCID 935—
SolventWaterHCID 962—
Product2-Methoxypyridine-4-carbaldehydeHCID 276299635.1%

Reaction Steps

A mixture of 2-methoxy-4-cyanopyridine (57.2 g), semicarbazide hydrochloride (71.24 g), sodium acetate (69.86 g), ethanol (1200 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 and evaporated to give 2-methoxypyridine-4-carboxaldehyde (20.53 g, 35%) m.p. 33°-35°. A sample recrystallised from petroleum ether had m.p. 33°-36°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539207
Source datasetuspto-grants-1985_09
ORD IDord-990dca3a38904e6185884daab2255492
Source noteuspto-grants-1985_09