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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979999Generated: October 29, 2026

Dimethylformamide → 2-[2-(Dimethylamino)-1-propenyl]-6-methoxy-3-pyridinecarbonitrile

https://huagongshe.com/reaction/979999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1,1-Dimethoxyethyl(dimethyl)amineHCID 87835—
Reactant2-Methoxy-5-pyridinecarbonitrileHCID 2736776—
Reactant6-Methoxy-2-methylpyridine-3-carbonitrileHCID 13749918—
SolventMethanolHCID 887—
Product2-[2-(Dimethylamino)-1-propenyl]-6-methoxy-3-pyridinecarbonitrileHCID 54307929—

Reaction Conditions

Temperature130 °C

Reaction Steps

2-2-(Dimethylamino)-1-propenyl]-6-methoxy-3-pyridinecarbonitrile--A mixture containing 47.2 g of 6-methoxy-2-methyl-3-pyridinecarbonitrile, 100 ml of dimethylacetamide dimethyl acetal and 100 ml of dimethylformamide was heated with stirring in an oil bath at 130° C. for 1 hour and 45 minutes. The temperature of the oil bath was raised to 150° C. and the methanol formed by the reaction was distilled off using a 12" distillation column (Vigreux) while continuing the heating at 150° C. for 14 hours. The reaction mixture was concentrated, 50 ml of ether was added to the concentrated solution whereupon the product crystallized out. The mixture was chilled and the crystalline solid collected. The solid was washed with cold ether, dried and recrystallized from ethyl acetate using decolorizing charcoal to yield 33.5 g of 2-[2-(dimethylamino)-1-propenyl]-6-methoxy-3-pyridinecarbonitrile, m.p. 103°-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04634772
Source datasetuspto-grants-1987_01
ORD IDord-e6816dcca2d94615bd188fd180027040
Source noteuspto-grants-1987_01