HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Cyclohexanecarbonitrile, 1-(1-naphthalenyl)-4-oxo-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 12230237 | HCID 12230237 | — |
| Solvent | Water | HCID 962 | — |
| Product | Cyclohexanecarbonitrile, 1-(1-naphthalenyl)-4-oxo- | HCID 12230240 | 76% |
Reaction Steps
A mixture of 16.73 g. (0.055 mole) of methyl 5-cyano-5-(1-naphthyl)-2-oxocyclohexanecarboxylate (prepared in Example 11) in 400 ml. of acetic acid and 200 ml. of 10% sulfuric acid is stirred mechanically for about 44 hours. The mixture is then allowed to cool and diluted with water. This mixture is extracted thoroughly with benzene. The organic layer is successively washed with water, sodium bicarbonate solution and brine and evaporated to dryness. The solid residue is recrystallized from acetone to give 10.3 g. (76% yield) of 4-cyano-4-(1-naphthyl)cyclohexanone, having a melting point of 213° to 215°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03979444 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-0c2df48257f54f2ca34ef7dc2613c2a0 |
| Source note | uspto-grants-1976_09 |