Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239957Generated: October 26, 2026

Imidazole → 4-((Tert-butyldimethylsilyl)oxy)piperidine

https://huagongshe.com/reaction/239957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantPiperidin-4-olHCID 79341—
SolventDichloromethaneHCID 6344—
Product4-((Tert-butyldimethylsilyl)oxy)piperidineHCID 11481328173.2%

Reaction Steps

To a solution of 4-hydroxypiperidine (2.00 g, 9.89 mmoles) in CH2Cl2 (30 mL) is added 1H-imidazole (2.69 g, 39.55 mmoles) followed by t-butyldimethylchlorosilane (3.58 g, 23.73 mmoles) and the reaction mixture is stirred at room temperature. After 12 hours, the reaction mixture is washed with water, saturated solution of NaHCO3, and brine. The organic layers are combined and dried over sodium sulfate, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) over a gradient using 100% CH2Cl2 to 10% 7N ammonia in MeOH/90% CH2Cl2 to afford the title compound (3.69 g, 86.3%). Mass spectrum (m/z): 216.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642768B2
Source datasetuspto-grants-2014_02
ORD IDord-f6f2b288a43f471d81bb0a04406fac5a
Source noteuspto-grants-2014_02