Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393505Generated: November 2, 2026

1H-1,2,4-Triazole → HCID 22372689, compound

https://huagongshe.com/reaction/2393505

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
Reactant2-(1-Chloroethyl)-9H-fluoreneHCID 14572484—
SolventWaterHCID 962—
ProductHCID 22372689HCID 22372689—

Reaction Conditions

Temperature120 °C

Reaction Steps

The thus obtained 2-(1-chloroethyl)-9H-fluorene was mixed with 1,2,4-triazole (1.31 g) and heated at 120° C. for 30 minutes without further adding solvent. After cooling, water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, the solvent was evaporated and then the resulting residue was subjected to silica gel column chromatography. First, elution was carried out with a mixed solvent of chloroform and methanol (50:1), and the thus obtained crude crystals were recrystallized from a mixed solvent of ether and ethyl acetate to obtain 0.24 g of 1-[1-(9H-fluoren-2-yl) ethyl]-1H-1,2,4-triazole (Example 5). Thereafter, crude crystals obtained from the chloroform-methanol (50:1) eluate were recrystallized from a mixed solvent of ethyl acetate and ether to obtain 0.25 g of 4-[1-(9H-fluoren-2-yl) ethyl]-4H-1,2,4-triazole (Example 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807880
Source datasetuspto-grants-1998_09
ORD IDord-53072c8fe8e541ee852c40d180f35759
Source noteuspto-grants-1998_09