HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluidine → 1-p-Tolylaminocyclohexanecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-p-Tolylaminocyclohexanecarbonitrile | HCID 59839099 | 93% |
Reaction Steps
Sodium cyanide (0.147 g, 3 mmol) was added to a mixture of p-toluidine (0.214 g, 2 mmol) and cyclohexanone (0.294 g, 3 mmol) in acetic acid 90% (3 ml). The reaction mixture was stirred at room temperature for 12 h and then 20 ml of ethyl acetate was added. The organic layer was washed with water (3×10 ml), dried over magnesium sulfate and concentrated under vacuum to dryness to yield 1-(4-methylphenyl)aminocyclohexanenitrile, 9a (0.398 g, 1.86 mmol, 93%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658681B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-540482f75dd243c79996ce8367492cc5 |
| Source note | uspto-grants-2014_02 |