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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383833Generated: November 1, 2026

Water → HCID 21187493, compound

https://huagongshe.com/reaction/1383833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-IodopropaneHCID 33643—
ReactantHCID 178455184HCID 178455184—
SolventDimethylformamideHCID 6228—
ProductHCID 21187493HCID 2118749343%
ProductHCID 21187495HCID 2118749531%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred mixture of sodium hydride (60% dispersion in oil, 1.5 g, 37.5 mmol) and 1-iodopropane (4.4 ml, 45 mmol) in anhydrous DMF (100 ml), cooled under nitrogen to 0° C., was added dropwise over 10 min a solution of 3-(tert-butyldimethylsilanyloxymethyl)-1H-1,2,4-triazole (prepared as described in EP-A-421210) (8.0 g, 37.5 mmol) in anhydrous DMF (25 ml). The mixture was stirred under nitrogen at 0° C. for 25 min, more sodium hydride (60% dispersion in oil, 0.45 g, 11.3 mmol) was added, and the mixture was stirred for another 30 min. Water (300 ml) was then added and the mixture was extracted with ethyl acetate (3×100 ml). The combined organic extracts were washed with brine (100 ml), dried (Na2SO4) and evaporated in vacuo. The residue was purified by flash chromatography (silica gel, 40-50% EtOAc/hexane; and alumina, 15% EtOAc/hexane) to yield 4.10 g (43%) of 5-(tert-butyldimethylsilanyloxymethyl)-1-propyl-1H-1,2,4-triazole and 2.97 g (31%) of 3-(tert-butyldimethylsilanyloxymethyl)-1-propyl-1H-1,2,4-triazole as colourless oils.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255305B1
Source datasetuspto-grants-2001_07
ORD IDord-20de30ae4ffe42ddbc563a85b1fee8c0
Source noteuspto-grants-2001_07