HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,3'-Bis(trifluoromethyl)benzophenone → bis[3-(trifluoromethyl)phenyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,3'-Bis(trifluoromethyl)benzophenone | HCID 599788 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | bis[3-(trifluoromethyl)phenyl]methanol | HCID 2736113 | 94% |
Reaction Steps
To a solution of 3,3′-bis(trifluoromethyl)benzophenone (11.4 g, 36 mmol) in MeOH (50 mL) was added sodium borohydride (1.9 ml, 53 mmol) portionwise at rt. The suspension was stirred at rt for 24 h. The reaction was diluted slowly with water and extracted with CH2Cl2. The organic was washed successively with water, brine, dried over Na2SO4, and concentrated to give bis(3-(trifluoromethyl)phenyl)methanol (10.8 g, 94% yield). The crude oil was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735383B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-5898359ff49a474bb2c8b1833a61239e |
| Source note | uspto-grants-2014_05 |