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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650768Generated: October 31, 2026

Ethanol → HCID 14624393, compound

https://huagongshe.com/reaction/1650768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 14858089HCID 14858089—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
ProductHCID 14624393HCID 14624393—

Reaction Steps

3.5 g (0.01 mol) of 3-(tert-butyl)-5-methylthio-1-(2,4,6-trichlorophenyl)-1H-1,2,4-triazole was added to 120 ml of 85% ethanol, and 24.6 g (0.04 mol) of Oxone (trade mark) was further added thereto. The mixture was stirred at room temperature for 4 hours. Then, water was added to such an extent that Oxone (as described above) remained in a small amount, and the mixture was extracted with dichloromethane. The dichloromethane layer was dried, and then the solvent was distilled off. The residue was purified by silica gel column chromatography to obtain 3.0 g (yield: 78.9 g) of the desired compound as white powder. Melting point: 179°-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925864
Source datasetuspto-grants-1990_05
ORD IDord-2924628c6b314f38aa6f089d0155ef49
Source noteuspto-grants-1990_05