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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81684Generated: October 30, 2026

Water → 2-cyclopropyl-4-nitro-2H-1,2,3-triazole

https://huagongshe.com/reaction/81684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-nitro-2H-1,2,3-triazoleHCID 278150—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantCyclopropylboronic acidHCID 2760897—
CatalystCupric acetateHCID 8895—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
Product2-cyclopropyl-4-nitro-2H-1,2,3-triazoleHCID 6842981218.4%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of 4-nitro-2H-1,2,3-triazole (1.0 g, 8.77 mmol), cyclopropylboronic acid (1.51 g, 17.5 mmol), copper (II) acetate (1.59 g, 8.77 mmol) and N,N-dimethylpyridin-4-amine (3.21 g, 26.3 mmol) in toluene (20 ml) was added sodium 1,1,1,3,3,3-hexamethyldisilazan-2-id (14.6 ml, 0.6M toluene solution) under oxygen atmosphere, and the mixture was stirred at 95° C. for 2 days. The reaction solution was cooled to room temperature, water was then added, the mixture was extracted with chloroform, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (Biotage, hexane:ethyl acetate=5:1 to 3:1) to give 2-cyclopropyl-4-nitro-2H-1,2,3-triazole (249 mg, yield: 18%) as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846700B2
Source datasetuspto-grants-2014_09
ORD IDord-7b1683ba2552434abef2b7a7aa0f2c4d
Source noteuspto-grants-2014_09