HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borane;tetrahydrofuran → (4-Bromo-3-(trifluoromethyl)phenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 4-Bromo-3-(trifluoromethyl)benzoic acid | HCID 24721390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Bromo-3-(trifluoromethyl)phenyl)methanol | HCID 45933700 | — |
Reaction Steps
To a solution of 4-bromo-3-(trifluoromethyl)benzoic acid 46-2 (1.35 g, 5 mmol) in THF (10 mL) was added 1M BH3.THF in THF (20 mL) slowly at 0° C. The mixture was warmed up to room temperature and stirred for 4 hours. The reaction was quenched with water at 0° C. All the solvents were evaporated and the residue was redissolved in ethyl acetate (100 mL), washed with saturated NaHCO3 aqueous solution, water and brine, dried over Na2SO4, and then concentrated. The crude product was purified by silica gel flash chromatography, eluted with 40% ethyl acetate in hexane to give (4-bromo-3-(trifluoromethyl)phenyl)methanol 46-3 as white solid. MS m/z 237.1 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238646B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-108c546b80b64ecba3619fd5bf3c5b78 |
| Source note | uspto-grants-2016_01 |