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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127192Generated: October 25, 2026

Ethanol → 6-Methoxypyridine-3-carbaldehyde

https://huagongshe.com/reaction/127192

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), 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°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255428
Source datasetuspto-grants-1981_03
ORD IDord-875292ae258549168306a618a2e45828
Source noteuspto-grants-1981_03