HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → {3-[2,4-Bis(trifluoromethyl)benzyl]-3-azabicyclo[3.3.1]non-7-yl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,4-Bis(trifluoromethyl)benzaldehyde | HCID 2736095 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86678702 | HCID 86678702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {3-[2,4-Bis(trifluoromethyl)benzyl]-3-azabicyclo[3.3.1]non-7-yl}methanol | HCID 86678703 | — |
Reaction Steps
To a solution of 3-azabicyclo[3.3.1]non-7-ylmethanol hydrochloride (2.54 g) in THF (66.2 mL) was added 2,4-bis(trifluoromethyl)benzaldehyde (2.82 mL). The reaction mixture was stirred at room temperature for 1 hr, and sodium triacetoxyborohydride (5.62 g) was added. The mixture was further stirred at room temperature for 30 min and poured into 0.1M aqueous sodium hydroxide solution, 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 (3.64 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772277B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-7989e75c0f5e47c8a7574d7ddecb7063 |
| Source note | uspto-grants-2014_07 |