Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677941Generated: October 30, 2026

Imidazole → (1S,3S)-3-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclopentanol

https://huagongshe.com/reaction/1677941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3-(Hydroxymethyl)cyclopentanolHCID 58651115—
SolventDimethylformamideHCID 6228—
Product(1S,3S)-3-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclopentanolHCID 6679796331%

Reaction Steps

To a solution of (1S,3S)-3-(hydroxymethyl)cyclopentanol (453.0 mg, 0.003276 mol) and 1H-imidazole (669 mg, 0.00983 mol) in DMF (35.8 mL) under an atmosphere of nitrogen was added tert-butyldimethylsilyl chloride (494 mg, 0.00328 mol). The mixture was stirred for 1.25 hours, then tert-butyldimethylsilyl chloride (49 mg, 0.00033 mol) was added. After an additional hour of stirring, the reaction was quenched with water, extracted with ethyl acetate (3×), dried with anhydrous Na2SO4, filtered, and concentrated. The residue was filtered through a plug of silica with 30% EtOAc/hexanes to obtain 234.1 mg (31%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008307B2
Source datasetuspto-grants-2011_08
ORD IDord-ce3c0f8818d44e0c92ed64ebf8c21344
Source noteuspto-grants-2011_08