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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070604Generated: October 31, 2026

Imidazole → Rac-[(1r,4r)-4-{[(tert-butyldimethylsilyl)oxy]methyl}cyclohexyl]methanol

https://huagongshe.com/reaction/2070604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant1,4-CyclohexanedimethanolHCID 7735—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantLithium BromideHCID 82050—
SolventDimethylformamideHCID 6228—
ProductRac-[(1r,4r)-4-{[(tert-butyldimethylsilyl)oxy]methyl}cyclohexyl]methanolHCID 1075372357%

Reaction Steps

To a solution of cyclohexane-1,4-dimethanol (10.0 g) in N,N-dimethylformamide (100 mL) were added successively tert-butyldimethylchlorosilane (8.9 g) and imidazole (9.5 g), followed by stirring the reaction mixture at room temperature for 16 hours. To the reaction mixture were added ice and saturated aqueous lithium bromide solution, followed by extraction with diethyl ether. The organic layer was washed with saturated aqueous lithium bromide solution and saturated brine, dried and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane (volume ratio)=1:9 to 2:3) to give [4-(tert-butyldimethylsilanyloxymethyl)-cyclohexyl]-methano 1 (8.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299296B2
Source datasetuspto-grants-2012_10
ORD IDord-72f6a98c68994e669277ac8ac7d92b24
Source noteuspto-grants-2012_10