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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477003Generated: November 1, 2026

Hydrochloric Acid → 4-Ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile

https://huagongshe.com/reaction/1477003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxygenHCID 977—
ReactantCyanoacetamideHCID 7898—
ReactantHexen-2-alHCID 12990—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product4-Ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrileHCID 1564180031.7%

Reaction Steps

To a stirred solution of t-BuOK (22.85 g, 204.08 mmol) and cyanoacetamide (18.8 g, 224.1 mmol) in DMSO (300 mL) was added hex-3-en-2-one (20 g, 204.08 mmol) under argon atmosphere at room temperature. The reaction mixture was then stirred at room temperature for 30 min and then added additional t-BuOK (68.5 g, 612.05 mmol) was added. Argon gas was displaced by oxygen gas and the mixture stirred for 48 hrs at room temperature in presence of oxygen. Reaction was monitored by TLC. The reaction mixture was cooled to 0° C. and diluted with water (100 mL) followed by 4 N HCl (120 mL). The mixture was stirred for 15 min and the resulting solid was filtered. The solid was washed with water (1 L) and dried to afford the title compound, 4-ethyl-1,2-dihydro-6-methyl-2-oxopyridine-3-carbonitrile (10.5 g, 31%), as an off white solid. 1H NMR (CDCl3, 400 MHz): δ ppm 1.148-1.185 (t, 3H, J=7.4 Hz), 2.237 (s, 3H), 2.557-2.614 (m, 2H), 6.211 (s, 1H), 12.330 (broad s, 1H). MS(ES) [M+1-1]+161.06.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09402836B2
Source datasetuspto-grants-2016_08
ORD IDord-3a5ae38a7fe24ae5b1558896d64ff4d6
Source noteuspto-grants-2016_08