HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N-(3,5-bis(trifluoromethyl)benzylidene)(2-chloro-5-(trifluoromethyl)phenyl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | P-Toluenesulfonamide | HCID 6269 | — |
| Reactant | 3,5-Bis(trifluoromethyl)benzaldehyde | HCID 136247 | — |
| Reactant | 2-Chloro-5-(trifluoromethyl)benzylamine | HCID 2736682 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(3,5-bis(trifluoromethyl)benzylidene)(2-chloro-5-(trifluoromethyl)phenyl)methanamine | HCID 86614963 | — |
Reaction Steps
To a 100 mL round bottom flask, equipped with a Dean Start Trap was charged 50 mL of toluene, 5.0 gm of 2-chloro-5-trifluoromethyl benzyl amine and 5.8 gm of 3,5-bis(trifluoromethyl)benzaldehyde and 50 mg of para-toluenesulfonamide. The reaction was heated until water no longer distilled off about 3 hours, then cooled to ambient temperature and the solvent removed in vacuum. The crude product was used directly in the next step without further purification. 10.0 gm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383660B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-52125c224296419883ebfc494951e33d |
| Source note | uspto-grants-2013_02 |