HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Benzyloxy)-alpha-(trifluoromethyl)benzyl Alcohol → 4-(2,2,2-Trifluoro-1-hydroxyethyl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Benzyloxy)-alpha-(trifluoromethyl)benzyl Alcohol | HCID 21252664 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-(2,2,2-Trifluoro-1-hydroxyethyl)phenol | HCID 11286977 | — |
Reaction Steps
At 50° C. and a hydrogen pressure of 5 bar, 65.7 g (233 mmol) of 1-benzyloxy-4-(1-hydroxy-2,2,2-trifluoroethyl)benzene were hydrogenated in the presence of 5.2 g of palladium (10% on carbon) in 500 ml of glacial acetic acid. The catalyst was filtered off and the mixture was concentrated. This gave 44.1 g (99% of theory) of the product as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06197729B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-166f643d580845d6bac7ff1b171f6f5c |
| Source note | uspto-grants-2001_03 |