HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluidine → 4-Chloro-N-(4-methylphenyl)-3-(trifluoromethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chloro-3-(trifluoromethyl)benzoyl chloride | HCID 3699691 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Chloro-N-(4-methylphenyl)-3-(trifluoromethyl)benzamide | HCID 68451232 | 97.2% |
Reaction Steps
To a solution of p-toluidine (0.44 g, 4.1 mmol) in 10 ml of CH2Cl2 (pre-cooled to 0° C.) are added Et3N (1.14 ml, 2 eq.) and 4-chloro-3-trifluoromethyl-benzoyl chloride (1 g, 4.1 mmol) in 5 ml of CH2Cl2. The mixture is slowly warmed to room temperature and continued to stir at room temperature for an hour. The mixture is diluted with 50 ml of CH2Cl2, washed with 1N HCl solution, and brine. The organic layer is separated, dried over MgSO4, filtered, and concentrated. The residue is purified by column chromatography (EtOAc/Hexanes, 2:3) to give 1.25 g (97%) of 4-chloro-N-p-tolyl-3-trifluoromethyl-benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07750021B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-913f2576eafb4c48a3b97c32da571193 |
| Source note | uspto-grants-2010_07 |