HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-(4-(Trifluoromethyl)phenyl)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | [4-(Trifluoromethyl)phenyl]acetaldehyde | HCID 14298210 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-(Trifluoromethyl)phenyl)ethan-1-ol | HCID 11275510 | 105.2% |
Reaction Steps
NaBH4 (2 g, 0.055 mol) was added at 0° C. to a solution of 4-trifluoromethyl-phenyl)-acetaldehyde (9.4 g, 0.05 mol, from step (ii) above) in 154 ml ethanol and stirred at RT overnight. The solvent was evaporated under reduced pressure and the residue was partitioned between 50 ml 1 N HCl and 50 ml diethyl ether. Organic layer was washed with water, dried over sodium sulfate and the solvent evaporated under reduced pressure to give 10 g of the sub-title compound as a liquid. This was directly taken for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07648985B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-cd6ee83844f3482e80fdf21ec8280d77 |
| Source note | uspto-grants-2010_01 |