HuagongsheHuagongshe Chemistry Print Report · For research reference only
2'-Trifluoromethyl (1,1'-biphenyl)-4-carboxylic acid → [2'-(Trifluoromethyl)[1,1'-biphenyl]-4-yl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2'-Trifluoromethyl (1,1'-biphenyl)-4-carboxylic acid | HCID 2782714 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2'-(Trifluoromethyl)[1,1'-biphenyl]-4-yl]methanol | HCID 1394132 | — |
Reaction Steps
To a solution of 4-(2'-trifluoromethylphenyl)benzoic acid (1.525 g, 5.728 mmol) in THF (25 mL) at 0° C. was added 1.0 M lithium aluminum hydride in tetrahydrofuran (12.0 mL, 12.0 mmol) over 10 minutes. The reaction was allowed to stir at ambient temperature for 3 hours, cooled to 0° C., and quenched by dropwise addition of water (0.5 mL), 4 N aq. NaOH (0.5 mL), and water (1.5 mL). The reaction was filtered through a pad of Celite and the filtrate evaporated in vacuo. The residue was chromatographed (Silica gel, 20% EtOAc in hexanes) to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06080870 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-07d6b03b541844a6a9d71e79e6297097 |
| Source note | uspto-grants-2000_06 |