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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742063Generated: November 3, 2026

4-Toluenesulfonyl chloride → 5-amino-3-methyl-1-(O-tosyl-3-nitrobenzohydroximoyl)-pyrazole

https://huagongshe.com/reaction/1742063

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant5-Amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazoleHCID 73508416—
SolventAcetonitrileHCID 6342—
Product5-amino-3-methyl-1-(O-tosyl-3-nitrobenzohydroximoyl)-pyrazoleHCID 7350841973.1%

Reaction Steps

7.4 g (0.028 mol) of 5-amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazole are treated in 90 ml of absolute acetonitrile with 4 ml (0.028 mol) of triethylamine and then, with stirring at room temperature, are treated dropwise with a solution of 5.55 g (0.029 mol) of 4-tosyl chloride in 150 ml of absolute acetonitrile. Stirring is continued for 1 hour and then the mixture is evaporated to dryness. The residue is treated with water and ethyl acetate, the organic phase is washed with water, dried over magnesium sulphate and evaporated under vacuum. The oily residue obtained in this way is crystallised from ethanol. 8.5 g (72%) of 5-amino-3-methyl-1-(O-tosyl-3-nitrobenzohydroximoyl)-pyrazole with a m. pt. of 156°-158° C. are obtained. The substance is light-sensitive. On recrystallising twice from ethanol, the m. pt. is 165°-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05336780
Source datasetuspto-grants-1994_08
ORD IDord-9e7aea21da4748b6b736179a167e9b9f
Source noteuspto-grants-1994_08