HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → (1-{1-[2,4-Bis(trifluoromethyl)phenyl]ethyl}piperidin-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (1-{1-[2,4-Bis(trifluoromethyl)phenyl]ethenyl}piperidin-4-yl)methanol | HCID 86678734 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1-{1-[2,4-Bis(trifluoromethyl)phenyl]ethyl}piperidin-4-yl)methanol | HCID 86678735 | 86% |
Reaction Steps
To a solution of (1-{1-[2,4-bis(trifluoromethyl)phenyl]ethenyl}piperidin-4-yl)methanol (12.6 g) in methanol (178 mL) was added sodium borohydride (2.02 g). The reaction mixture was stirred at room temperature for 20 min, saturated aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (10.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772277B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-08494a3b9f0d4416bf3d8b0e1a6044c9 |
| Source note | uspto-grants-2014_07 |