HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-(Benzyloxy)-alpha-(trifluoromethyl)benzyl Alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(4-(Benzyloxy)phenyl)-2,2,2-trifluoroethanone | HCID 21252691 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(Benzyloxy)-alpha-(trifluoromethyl)benzyl Alcohol | HCID 21252664 | — |
Reaction Steps
At 20° C., a solution of 15.7 g of sodium borohydride in 100 ml of water was added dropwise with cooling to a solution of 72.5 g of 4′-benzyloxy-2,2,2-trifluoroacetophenone in 900 ml of ethanol. The mixture was stirred under reflux for 3 hours and then concentrated, the residue was taken up in diethyl ether and water and made slightly acidic using dilute hydrochloric acid, and the organic phase was dried and concentrated to give the title 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-4a92d3c83db041b38275b9daed4ffa74 |
| Source note | uspto-grants-2001_03 |