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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244913Generated: October 26, 2026

1H-1,2,4-Triazole → 4-[1,2,4]Triazol-1-yl-cyclohexanone

https://huagongshe.com/reaction/244913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantSodium hydrideHCID 24758—
Reactant1,4-Dioxaspiro(4.5)decan-8-yl methanesulfonateHCID 14966741—
SolventDimethylformamideHCID 6228—
Product4-[1,2,4]Triazol-1-yl-cyclohexanoneHCID 57424093—
Product1-(1,4-dioxa-spiro[4.5]dec-8-yl)-1H-[1,2,4]triazoleHCID 57424096—

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of methanesulfonic acid 1,4-dioxa-spiro[4.5]dec-8-yl ester (567 mg, 2.40 mmol) and 1,2,4-triazole (232 mg, 3.36 mmol) in dry DMF (5.00 mL) is treated with sodium hydride 60% (125 mg, 3.12 mmol) at room temperature under nitrogen. The resulting mixture is stirred at 65° C. for 72 h. It is poured in ice water (75 mL), extracted 3 portions of 75 mL of EtOAc. The organic portions are combined, dried over anhydrous Na2SO4 and concentrated. The solid is purified by silica gel column chromatography using a gradient from 100% EtOAc to 5% MeOH:EtOAc as eluent to furnish the final compound 1-(1,4-dioxa-spiro[4.5]dec-8-yl)-1H-[1,2,4]triazole as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658674B2
Source datasetuspto-grants-2014_02
ORD IDord-4ee57366ead144b184bf83e9e5e413fa
Source noteuspto-grants-2014_02