HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 21552967, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21552950 | HCID 21552950 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21552967 | HCID 21552967 | — |
Reaction Steps
To 62.3 g (0.12 mole) of 4'-tert-butyl-5-[4-(α-hydroxy-α-phenylbenzyl)piperidino]valerophenone hydrochloride dissolved in about 1200 ml of methanol is added methanolic potassium hydroxide until the solution is basic. The solution is cooled in an ice bath with stirring and 5 g (0.13 mole) of sodium borohydride is added portionwise. The mixture is stirred an additional half hour, allowed to warm to room temperature then heated on a steam bath for half an hour. The solvent is removed at reduced pressure and the remaining residue is washed with water and recrystallized from acetone to give α-(p-tert-butylphenyl)-4-(α-hydroxy-α-phenylbenzyl)-1-piperidine-pentanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03946022 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-df67968109384b588019d993272192fe |
| Source note | uspto-grants-1976_03 |