HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605679Generated: October 31, 2026
Hydrochloric Acid → α-(Dimethylamino)-2-pyridineacetonitrile
https://huagongshe.com/reaction/1605679
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Solvent | Water | HCID 962 | — |
| Product | α-(Dimethylamino)-2-pyridineacetonitrile | HCID 15166870 | — |
Reaction Steps
To cold 2-pyridinecarboxaldehyde (21.4 g., 0.2 mole) is added dimethylamine (22.5 g. of a 40% aqueous solution, 0.2 mole) and the solution is neutralized with concentrated hydrochloric acid. To the stirred neutralized solution is added 14.4 g. (0.22 mole) of potassium cyanide. The mixture is stirred overnight, then diluted with water, transferred to a separatory funnel and repeatedly extracted with chloroform. The combined chloroform extracts are washed 3 times with water, once with brine and dried over magnesium sulfate. The mixture is filtered, the solvent is removed under reduced pressure and methanol is added to the residue. The mixture is allowed to stand at -20°C. for 18 hours, then filtered. The filtrate is concentrated and distilled in vacuo to give 2-dimethylamino-2-(2-pyridyl)acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03950522 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-bef9b3d7c7114b29bc3b0cbf45a3e035 |
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| Source note | uspto-grants-1976_04 |
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