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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277157Erstellt: 24. Oktober 2026

4-Methylbenzyl chloride → 1-(4-Methylbenzyl)piperidin-4-ol

https://huagongshe.com/de/reaction/277157

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Methylbenzyl chlorideHCID 7722—
EduktPotassium CarbonateHCID 11430—
EduktPiperidin-4-olHCID 79341—
Lösungsmitteltert-ButanolHCID 6386—
Produkt1-(4-Methylbenzyl)piperidin-4-olHCID 79148251,6%

Reaktionsschritte

Synthesis of this compound was accomplished according to Scheme 33. To 5.05 g (50 mmol) of 4-hydroxypiperidine and 7.08 g (50 mmol) of p-methylbenzyl chloride in 25 mL of tert-butanol was added excess solid potassium carbonate, and the mixture was heated on a steam bath for 3 h. The mixture was cooled to room temperature and partitioned between ether and water. The organic phase was extracted with cold dilute HCl, and the acidic aqueous phase was extracted with ether twice. The aqueous phase was made basic with ice and 50% aqueous NaOH and extracted with ether. The ether phase was washed with dilute aqueous sodium bicarbonate solution, brine, dried, and evaporated under vacuum to give 5.3 g (52) of 1-(4-methylbenzyl)-4-hydroxypiperidine (123) as an oil. GC/MS showed 100% purity with a molecular ion of 205.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06355660B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-40bf85493a0040dfb069d802b5653eb2
Quellennotizuspto-grants-2002_03