HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(4,4,4-Trifluorobutoxy)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(Benzyloxy)-4-(4,4,4-trifluorobutoxy)benzene | HCID 67455899 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4,4,4-Trifluorobutoxy)phenol | HCID 67454964 | 96.5% |
Reaction Steps
60 g (193 mmol) of 1-(benzyloxy)-4-(4,4,4-trifluorobutoxy)benzene, and 7.61 g of Pd/C are dissolved in 900 mL of THF. 5 mL of triethylamine are added to the suspension. The reaction is hydrogenated under atmospheric pressure for 2 hours. The suspension is filtrated of 400 g of hyflo. The organic phase is concentrated under reduced pressure. Filtration of the residue on 900 g silica gel using toluene:ethyl acetate 4:1 as eluent and concentration under reduced pressure yields 41 g of 4-(4,4,4-trifluorobutoxy)phenol as a reddish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09097938B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-ef1aa17e29614c69bf6b09f8c1eaa6b5 |
| Source note | uspto-grants-2015_08 |