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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248291Generated: October 31, 2026

Semicarbazide hydrochloride → 2-Chloro-5,6-dimethylnicotinaldehyde

https://huagongshe.com/reaction/1248291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSemicarbazide hydrochlorideHCID 11236—
ReactantSodium AcetateHCID 517045—
Reactant2-Chloro-5,6-dimethylpyridine-3-carbonitrileHCID 12891106—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Chloro-5,6-dimethylnicotinaldehydeHCID 1278384660.5%

Reaction Steps

A mixture of 2-chloro-3-cyano-5,6-dimethylpyridine (21.5 g), semicarbazide hydrochloride (24.0 g), sodium acetate (42.3 g), water (225 ml) and methanol (475 ml) was hydrogenated at 344 kPa at 50° using Raney nickel catalyst (5 g). The mixture was added to water (750 ml) and filtered. The solid filtered off was suspended in water (130 ml) and concentrated hydrochloric acid (70 ml) was added and the mixture was heated at 100° for 1 hour; formalin (40% w/w, 120 ml) was added and the mixture was heated at 100° for a further 0.5 hour and allowed to cool. Sodium acetate (95 g) and water (250 ml) were added and the mixture was extracted with ether and the extracts were washed with 5% aqueous potassium carbonate and evaporated to give 2-chloro-5,6-dimethyl-3-pyridinecarboxaldehyde (13.24 g, 60%), m.p. 69°-70°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04523015
Source datasetuspto-grants-1985_06
ORD IDord-51f558f1b2bf4e0cbac82de8f5137951
Source noteuspto-grants-1985_06