HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-(2,2,2-Trifluoroethyl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(1-Chloro-2,2,2-trifluoroethyl)phenol | HCID 11458494 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2,2,2-Trifluoroethyl)phenol | HCID 22485360 | — |
Reaction Steps
To a solution of 4-(1-chloro-2,2,2-trifluoroethyl)phenol (3.60 g, 17.1 mmol) in THF was added sodium borohydride (0.903 ml, 25.6 mmol) in one portion. The reaction was stirred at RT for 18 h, and then quenched with MeOH. The resulting mixture was concentrated and diluted with EtOAc. After washed with water and brine. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was dried in vacuum to afford 4-(2,2,2-trifluoroethyl)phenol as a colorless oil. MS m/z: 175(M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745484B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-003fc360faab496482ebd362427b4fc9 |
| Source note | uspto-grants-2010_06 |