HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N-biphenyl-2-yl-2-(3,5-bis-trifluoromethyl-phenyl)-N-methyl-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3,5-Bis(trifluoromethyl)phenylacetic acid | HCID 123587 | — |
| Reactant | N-Methylbiphenyl-2-amine | HCID 12246986 | — |
| Product | N-biphenyl-2-yl-2-(3,5-bis-trifluoromethyl-phenyl)-N-methyl-acetamide | HCID 18546495 | 46% |
Reaction Steps
To a solution of 272 mg (1.0 mmol) 3,5-bis(trifluoromethyl)phenylacetic acid in 1 ml tetrahydrofuran 162 mg (1.0 mmol) 1,1′-carbonyldiimidazole was added in one portion at 0°. The reaction mixture was stirred for 2 hrs at room temperature and 147 mg (0.8 mmol) biphenyl-2-yl-methyl-amine was added. Stirring was continued for 3 days at room temperature. The reaction mixture was evaporated and the residue was purified by chromatography (SiO2, hexane/ethyl acetate 3:1) to give 160 mg (46%) N-biphenyl-2-yl-2-(3,5-bis-trifluoromethyl-phenyl)-N-methyl-acetamide as white crystals, MS (ISP): 438.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06552088B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-c14c6db555d34f5c90c953f0f1bdc8a5 |
| Source note | uspto-grants-2003_04 |