Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361840Generated: October 30, 2026

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

https://huagongshe.com/reaction/1361840

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 numberUS07880013B2
Source datasetuspto-grants-2011_02
ORD IDord-e8b25028b1d94faa91b5981708d247da
Source noteuspto-grants-2011_02