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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454112Generated: October 30, 2026

Imidazole → 3-(Tertbutyldimethylsilyloxy)-1-(1,2,4-triazol-1-yl)propane

https://huagongshe.com/reaction/454112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3-(1H-1,2,4-triazol-1-yl)propan-1-olHCID 4711802—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Product3-(Tertbutyldimethylsilyloxy)-1-(1,2,4-triazol-1-yl)propaneHCID 2203089784%

Reaction Steps

To a solution of 3-(1,2,4-triazol-1-yl)propan-1-ol (7 g, 55 mmol) in DMF (70 ml) was added tertbutyldimethylsilyl chloride (9.1 g, 60 mmol) followed by DMAP (336 mg, 2.7 mmol) followed by imidazole (4.5gr, 66 mmol). After stirring overnight at ambient temperature, the volatiles were removed under vacuum and the residue was partitioned between water and ethyl acetate/ether. The organic layer was separated, washed with water, brine, dried (MgSO4) and evaporated. The residue was purified by column chromatography eluting with methylene chloride/ether (6/4) to give 3-(tertbutyldimethylsilyloxy)-1-(1,2,4-triazol-1-yl)propane (11.1 gr, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-024284ce831e40c1a215f56582a77156
Source noteuspto-grants-2013_07