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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876004Generated: October 26, 2026

Imidazole → 4-Piperidineethanol TBS

https://huagongshe.com/reaction/876004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-PiperidineethanolHCID 73953—
SolventDichloromethaneHCID 6344—
Product4-Piperidineethanol TBSHCID 1622075986%

Reaction Steps

2-(piperidin-4-yl)ethanol (2.00 g, 15.5 mmol), t-butylchlorodimethylsilane (2.57 g, 17.0 mmol), and imidazole (1.05 g, 15.5 mmol) were taken up in dichloromethane (15 mL) and stirred for 22 hours. This solution was added to aqueous K2CO3 (80 mL) and extracted with dichloromethane (3×30 mL). The combined organics were dried (MgSO4) and evaporated to give a pale yellow oil. Silica gel chromatography (gradient elution dichloromethane+2.5% TEA/0-10% methanol) afforded a white solid. This solid was added to aqueous K2CO3 (60 mL) and extracted with dichloromethane+10% methanol (3×30 mL), the organics dried (MgSO4) and evaporated to give compound 292 as a yellow oil (3.24 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980903B2
Source datasetuspto-grants-2015_03
ORD IDord-4c27c03d82f543bc8904ec22e1c6d194
Source noteuspto-grants-2015_03