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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238782Generated: November 2, 2026

Imidazole → Ethyl 4-((tert-butyldimethylsilyl)oxy)cyclohexanecarboxylate

https://huagongshe.com/reaction/2238782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantEthyl 4-hydroxycyclohexanecarboxylateHCID 86973—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-((tert-butyldimethylsilyl)oxy)cyclohexanecarboxylateHCID 23144129100%

Reaction Steps

Ethyl 4-hydroxycyclohexanecaboxylate (3.44 g, 20.0 mmol) was dissolved in DMF (7 mL), and imidazole (3.40 g, 50.0 mmol) and tert-butyldimethylsilyl chloride (3.62 g, 24 mmol) were added thereto, followed by stirring overnight at room temperature. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=10:1) to afford ethyl 4-(tert-butyldimethylsilyloxy)cyclohexanecarboxylate (5.73 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718808B2
Source datasetuspto-grants-2010_05
ORD IDord-0d570ca3b9f54f119c6dbb57793586be
Source noteuspto-grants-2010_05