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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427111Generated: November 2, 2026

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

https://huagongshe.com/reaction/1427111

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 numberUS08933098B2
Source datasetuspto-grants-2015_01
ORD IDord-8bab4b111701408d911f8f924928a6ff
Source noteuspto-grants-2015_01