HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637964Generated: October 27, 2026
Dimethylformamide dimethyl acetal → 1,2-Dihydro-6-(2-dimethylaminoethenyl)-2-oxo-5-(n-propanoyl)-3-pyridinecarbonitrile
https://huagongshe.com/reaction/637964
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 6-Methyl-2-oxo-5-propanoyl-1,2-dihydropyridine-3-carbonitrile | HCID 13232038 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,2-Dihydro-6-(2-dimethylaminoethenyl)-2-oxo-5-(n-propanoyl)-3-pyridinecarbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04559347 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-d5dc6caf1c43490e8650e1e28a8bce9e |
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| Source note | uspto-grants-1985_12 |
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