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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993868Generated: October 31, 2026

Imidazole → Cyclopentanol, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, trans-

https://huagongshe.com/reaction/1993868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1,3-CyclopropanediolHCID 18699327—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductCyclopentanol, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, trans-HCID 5871506454.9%

Reaction Steps

To a stirred solution of 1,3-cyclopropanediol (5 g, 49 mmol) and imidazole (5 g, 73.4 mmol) in DMF (20 mL) was added t-butyldimethylsilyl chloride (5.2 g, 34.5 mmol) and the mixture was stirred for 90 minutes at room temperature. The mixture was diluted with brine (200 mL) and extracted with ether three times (1×100 mL and 2×50 mL). Each extract was washed with a portion of brine. The organic phases were combined, dried over sodium sulfate and evaporated to dryness. The mixture of cis/trans isomers was purified by column chromatography using ether and hexanes to give the predominant trans-3-(tert-butyl-dimethyl-silanyloxy)-cyclopentanol as a colorless liquid (4.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652053B2
Source datasetuspto-grants-2010_01
ORD IDord-235cd75dbb4947a59f15230ae65ab638
Source noteuspto-grants-2010_01