HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluidine → 1-(4-Methylphenyl)aminocyclobutanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Methylphenyl)aminocyclobutanenitrile | HCID 60987776 | 98% |
Reaction Steps
Trimethylsilyl cyanide (0.93 ml, 7 mmol) was added dropwise to a mixture of p-toluidine (0.535 g, 5 mmol) and cyclobutanone (0.42 g, 6 mmol). The reaction mixture was stirred at room temperature for 6 h and then concentrated under vacuum to obtain a brown liquid which was subjected to chromatography (dichloromethane) to yield 1-(4-methylphenyl)aminocyclobutanenitrile, 7a (0.912 g, 4.9 mmol, 98%) as a yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709517B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-91567efef80c4dea9d6bcb5a9020c4dd |
| Source note | uspto-grants-2010_05 |