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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 267193Erstellt: 23. Oktober 2026

Potassium borohydride → 4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]-alpha-phenyl-1-piperidinebutanol

https://huagongshe.com/de/reaction/267193

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium borohydrideHCID 4192641—
EduktSodium MethoxideHCID 10942334—
Edukt4-[4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]piperidino]butyrophenone hydrochlorideHCID 21555731—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]-alpha-phenyl-1-piperidinebutanolHCID 21555715—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03941795
Quelldatensatzuspto-grants-1976_03
ORD IDord-31d54994f1804563936e334fbdce7530
Quellennotizuspto-grants-1976_03