HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium borohydride → 4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]-alpha-phenyl-1-piperidinebutanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-[4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]piperidino]butyrophenone hydrochloride | HCID 21555731 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]-alpha-phenyl-1-piperidinebutanol | HCID 21555715 | — |
Reaction Steps
To a mixture of 4.2 g (0.0083 mole) of 4-[4-[α-(p tert-butylphenyl)-α-hydroxybenzyl]piperidino]butyrophenone hydrochloride and 0.54 g (0.01 mole) of sodium methoxide in 25 ml of methanol is added 2.16 g (0.04 mole) of potassium borohydride. The reaction mixture is stirred overnight, diluted with water and the methanol removed under reduced pressure. The remaining material is extracted with chloroform, washed with water, dried over magnesium sulfate and filtered. The filtrate is concentrated, and the residue is recrystallized from acetone-water to give 4-[α-(p-tert-butylphenyl)-α-hydroxybenzyl]-α-phenyl-1-piperidinebutanol, M.P. 161°-163°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03941795 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-31d54994f1804563936e334fbdce7530 |
| Source note | uspto-grants-1976_03 |