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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224880Generated: October 26, 2026

Ethanol → 6-Methoxypyridine-3-carbaldehyde

https://huagongshe.com/reaction/224880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSemicarbazide hydrochlorideHCID 11236—
ReactantSodium AcetateHCID 517045—
Reactant2-Methoxy-5-pyridinecarbonitrileHCID 2736776—
CatalystNickelHCID 935—
SolventWaterHCID 962—
Product6-Methoxypyridine-3-carbaldehydeHCID 336457650.3%

Reaction Steps

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°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04234588
Source datasetuspto-grants-1980_11
ORD IDord-c2900c37ae4746098799c15968b2f5e7
Source noteuspto-grants-1980_11