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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521178Generated: October 25, 2026

Imidazole → HCID 89473262, compound

https://huagongshe.com/reaction/521178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant5-Hydroxycyclohex-1-ene-1-carbonitrileHCID 60160564—
SolventDimethylformamideHCID 6228—
ProductHCID 89473262HCID 89473262—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Hydroxycyclohex-1-ene-1-carbonitrile (500 mg, 4.06 mmol) was dissolved in anhydrous DMF (5.1 mL) and then cooled to 0° C. Imidazole (276 mg, 4.06 mmol) and TBS-Cl (612 mg, 4.06 mmol) were added and the reaction mixture was allowed to stir at 0° C. for 2 hours. The reaction mixture was partitioned between water and DCM. The organic layer was collected and the aqueous layer was again extracted with DCM. The combined organic extracts were washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue was purified by MPLC on silica gel (using a gradient elution of 0-100%, EtOAc/hexanes) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328099B2
Source datasetuspto-grants-2016_05
ORD IDord-057fe3cbcde64e6493f9de8de4f18dbc
Source noteuspto-grants-2016_05