HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminobenzonitrile → N-(2-cyanophenyl)cyclohexanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminobenzonitrile | HCID 72913 | — |
| Reactant | N-[2-(trifluoromethyl)phenyl]cyclohexanecarboxamide | HCID 1367212 | — |
| Product | N-(2-cyanophenyl)cyclohexanecarboxamide | HCID 724309 | 75% |
Reaction Steps
This compound was prepared following the procedure described for compound 26A in example 26, except that 2-cyanoaniline was used in place of 2-trifluoromethylaniline. Yield 75%. M.p. 135-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399614B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-0654ae5f8d8e40b8bd6cce858f9e542d |
| Source note | uspto-grants-2002_06 |