Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280663Generated: October 29, 2026

Hydrogen Peroxide → HCID 13649672, compound

https://huagongshe.com/reaction/280663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13649671HCID 13649671—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 13649672HCID 1364967295.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution of 5-amino-1-(4-[4-chlorophenylthio]-3,5-dichlorobenzyl)-1,2,3-triazole-4-carboxamide (176 mg, 0.409 mmol) in glacial acetic acid (10 ml) was treated at ambient temperature with trifluoroacetic acid (94.3 μl, 139 mg, 1.23 mmol) and 30% aqueous hydrogen peroxide (2.72 ml). The mixture was stirred 45 minutes, diluted with glacial acetic acid (3.0 ml), stirred 3.25 hours, and diluted with water (100 ml). The mixture was cooled to 0° C., a small volume of diethyl ether was added, the mixture was carefully basified by addition of 50% (w/v) aqueous sodium hydroxide, and diethyl ether was evaporated under vacuum. The resulting suspension was filtered, and the solid washed well with water and dried at 45° C. under vacuum to provide 173 mg (95%) of 5-amino-1-(4-[4-chlorophenylsulfinyl]-3,5-dichlorobenzyl)-1,2,3-triazole-4-carboxamide. Recrystallization from ethanol provided material of m.p. 195°-197 ° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04590201
Source datasetuspto-grants-1986_05
ORD IDord-763688de1d504fa895fbce158daf8779
Source noteuspto-grants-1986_05