HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 14257858, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14257846 | HCID 14257846 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14257858 | HCID 14257858 | — |
Reaction Steps
To a solution of [1-(2-phenylethyl)-4-piperidinyl][3-(trifluoromethyl)-phenyl]-methanone (2.8 g, 7.75 mmol) in methanol (50 ml) cooled in an ice bath was added portionwise sodium borohydride (0.3 g, 7.75 mmol). The reaction was allowed to warm to room temperature and stirred an additional 4 h. The mixture was evaporated and the residue extracted with Et2O, washed with H2O (3×100 ml), saturated aqueous NaCl (1×100 ml), dried (Mg SO4), filtered and evaporated to give a white solid. This solid was recrystallized from ether-hexane to give white needles, mp 143°-147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04912117 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-a200fa468f024c46924ae14227302b4d |
| Source note | uspto-grants-1990_03 |