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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875999Generated: October 26, 2026

Imidazole → 4-{[(Tert-butyldimethylsilyl)oxy]methyl}piperidine

https://huagongshe.com/reaction/875999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-PiperidinemethanolHCID 420771—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product4-{[(Tert-butyldimethylsilyl)oxy]methyl}piperidineHCID 6702199495.4%

Reaction Steps

Piperidin-4-ylmethanol (2.50 g, 21.7 mmol), t-butylchlorodimethylsilane (4.13 g, 23.9 mmol), and imidazole (1.48 g, 21.7 mmol) were dissolved in dichloromethane (25 mL) and stirred at room temperature for 18 hours. The reaction was added to aqueous NaHCO3 (200 mL, 50% saturated) and extracted with dichloromethane (3×150 mL). The combined organics were dried (MgSO4) and evaporated to give a yellow oil. Silica gel chromatography (gradient elution dichloromethane+2.5% TEA/0-10% methanol) gave a soft white solid, which was then added to 0.5 M NaOH (100 mL) and extracted with dichloromethane+10% methanol (3×100 mL). The combined organics were dried (MgSO4) and evaporated to give compound 284 as a pale yellow oil (4.75 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980903B2
Source datasetuspto-grants-2015_03
ORD IDord-c77b6a2813dd451d89174c5b81542e09
Source noteuspto-grants-2015_03