Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Nonyn-2-one, 9-chloro- | HCID 11435214 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Decynenitrile, 9-oxo- | HCID 11400960 | — |
Reaction Steps
To a solution consisting of 2.77 parts of 9-chloro-5-nonyn-2-one in 8 parts by volume of ethanol is added a solution containing 2.77 parts of sodium cyanide dissolved in 4 parts of water. The resulting reaction mixture is heated at 80° - 100° C. for about 24 hours, then is cooled and diluted with ether, and then 20 parts by volume of dilute aqueous sodium hydroxide is added with stirring. The layers are separated and the alkaline layer is extracted with ether. The ether extracts are combined, washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford 9-cyano-5-nonyn-2-one. This compound exhibits an infrared adsorption maximum at 2250 reciprocal centimeters and nuclear magnetic resonance peaks at δ2.15 and δ2.50.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04087621 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-b66a8562efc74edaae802b71612ecafb |
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| Source note | uspto-grants-1978_05 |
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