HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(3-Bromo-4-Methylphenyl)-3-(Trifluoromethyl)Benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(Trifluoromethyl)benzoyl chloride | HCID 75257 | — |
| Reactant | Benzenamine, 3-bromo-4-methyl- | HCID 82187 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-Bromo-4-Methylphenyl)-3-(Trifluoromethyl)Benzamide | HCID 58601069 | — |
Reaction Steps
To a solution of 3-bromo-4-methylbenzenamine (0.82 g, 4.4 mmol) in anhydrous CH2Cl2 (40 mL) was added 3-(trifluoromethyl)benzoyl chloride (0.72 ml, 4.85 mmol) and triethylamine (2.5 ml, 17.6 mmol). The mixture was stirred overnight at room temperature. The saturated NaHCO3 (80 mL) was added and the mixture was stirred for 5 min. The organic layer was separated and aqueous was extracted with CH2Cl2 (3×20 mL). The combined organic solution was dried (Na2SO4). The solvent was removed in vacuo. The title compound was afforded as a yellow solid (1.48 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030487B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-8abe591edd99402e9437bd66916ede94 |
| Source note | uspto-grants-2011_10 |