HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → N-(1-Cyanonaphthalen-2-yl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-amino-1-naphthonitrile | HCID 238860 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(1-Cyanonaphthalen-2-yl)benzamide | HCID 12758535 | — |
Reaction Steps
3.0 g (17.8 millimoles) of 2-aminonaphthalene-1-carbonitrile (Chem. Pharm. Bull 33 (4) (1985), 1360-1366) were stirred with 2.5 g (18.1 millimoles) of benzoyl chloride and 4 ml of triethylamine in 100 ml of toluene for 15 hours at 80° C. After the end of the reaction, the product was filtered off and dried. 1.5 g (31% of theory) of the title compound of melting point 205° C. (active ingredient example 1008) were obtained in this manner.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05035736 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-147943f0b63d4037b85f37ff46dad673 |
| Source note | uspto-grants-1991_07 |