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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249342Generated: October 27, 2026

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

https://huagongshe.com/reaction/2249342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylbenzyl chlorideHCID 7722—
ReactantPotassium CarbonateHCID 11430—
ReactantPiperidin-4-olHCID 79341—
Solventtert-ButanolHCID 6386—
Product1-(4-Methylbenzyl)piperidin-4-olHCID 79148251.6%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039991E1
Source datasetuspto-grants-2008_01
ORD IDord-8ed44f0ca2144ca3b608b303e6eb1dd3
Source noteuspto-grants-2008_01