HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Benzylbenzoic acid → 2-Benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Benzylbenzoic acid | HCID 11924 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 3,5-Bis(trifluoromethyl)benzylamine | HCID 521099 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-benzamide | HCID 9824373 | 49% |
Reaction Steps
To a solution of 255 mg (1.2 mmol) 2-benzylbenzoic acid in 1.5 ml tetrahydrofuran at 0° C. were added 195 mg (1.2 mmol) 1,1′-carbonyldiimidazole. After stirring for 2.5 h at room temperature, a solution of 243 mg (1.0 mmol) 3,5 bis(trifluoromethyl)benzylamine in 0.5 ml tetrahydrofuran was added and stirring was continued overnight. The solvent was removed in vacuo and the residue was purified by flash chromatography to give 210 mg (49%) of the title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06596773B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-d1857aea3757476a9b3976ae0995923a |
| Source note | uspto-grants-2003_07 |