HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-Pentyl-N-[4'-(trifluoromethyl)-1,1'-biphenyl-3-yl]amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Pentanal | HCID 8063 | — |
| Reactant | 4'-(Trifluoromethyl)-[1,1'-biphenyl]-3-amine | HCID 2782708 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Pentyl-N-[4'-(trifluoromethyl)-1,1'-biphenyl-3-yl]amine | HCID 18448425 | 43.9% |
Reaction Steps
To a solution of 4′-(trifluoromethyl)-1,1′-biphenyl-3-ylamine (0.3 g, 1.26 mmol) in anhydrous CH2Cl2 (10 mL) under nitrogen at room temperature was added valeraldehyde (0.134 mL, 1.26 mmol), sodium triacetoxyborohydride (0.374 g, 1.76 mmol) and acetic acid (72 μl, 1.26 mmol). The resultant mixture was stirred for 17 h at room temperature. The reaction mixture was quenched with sat. NaHCO3 aq. (15 mL), then extracted with CH2Cl2 (2×20 mL). The organic solution was dried (Na2SO4) and the solvent was removed in vacuo. Purification by SPE (20 g Silica column) eluted with 1:200 EtOAc:cyclohexane afforded the title compound as a colourless oil (0.17 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199239B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-f2d85215920c4a6aab57ab877bc6c10f |
| Source note | uspto-grants-2007_04 |