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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538680Generated: October 29, 2026

Benzyl Bromide → 2-(1-Benzylpiperidin-2-yl)ethan-1-ol

https://huagongshe.com/reaction/538680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Piperidin-2-ylethanolHCID 15144—
SolventEthanolHCID 702—
Product2-(1-Benzylpiperidin-2-yl)ethan-1-olHCID 10242551—

Reaction Steps

To a stirred solution of piperidine-2-ethanol (20 g, 155 mmol) in ethanol (240 mL) was added K2CO3 (106 g, 775.1 mmol) followed by addition of benzyl bromide (18.4 mL, 155.04 mmol) at 0° C. The reaction mixture was stirred at rt overnight, filtered through a sintered funnel and concentrated. The crude material was dissolved in ethyl acetate, the organic layer was washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated to get liquid compound 49.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865741B2
Source datasetuspto-grants-2014_10
ORD IDord-8d761a23fb7743ddb3bb6b93c5fa14c2
Source noteuspto-grants-2014_10