Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649161Generated: October 31, 2026

Dimethylformamide dimethyl acetal → 1,2-Dihydro-6-(2-dimethylaminoethenyl)-2-oxo-5-(n-propanoyl)-3-pyridinecarbonitrile

https://huagongshe.com/reaction/1649161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant6-Methyl-2-oxo-5-propanoyl-1,2-dihydropyridine-3-carbonitrileHCID 13232038—
SolventDimethylformamideHCID 6228—
Product1,2-Dihydro-6-(2-dimethylaminoethenyl)-2-oxo-5-(n-propanoyl)-3-pyridinecarbonitrileHCID 54067468—

Reaction Steps

A mixture containing 9.5 g of 1,2-dihydro-6-methyl-2-oxo-5-(n-propanoyl)-3-pyridinecarbonitrile, 50 ml of dimethylformamide and 8 ml of dimethylformamide dimethyl acetal was stirred at room temperature overnight and then concentrated to dryness on a rotary evaporator. The residue was refluxed with isopropyl alcohol; the insoluble yellow solid was collected, washed with isopropyl alcohol and dried at 90° C. to yield 2.8 g of 1,2-dihydro-6-(2-dimethylaminoethenyl)-2-oxo-5-(n-propanoyl)-3-pyridinecarbonitrile, m.p. 278°-280° C. with decomposition. The mother liquor was treated with decolorizing charcoal, filtered and concentrated to about 150 ml and allowed to stand at room temperature. The product that separated was collected, washed with isopropyl alcohol and dried to yield another 1.8 g of product, m.p. 270° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415580
Source datasetuspto-grants-1983_11
ORD IDord-d55feac1216f4c64b870bcbb0e9c5c5b
Source noteuspto-grants-1983_11