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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441532Generated: October 30, 2026

Cyclohexane → 4-(Benzenesulfonyl)-1-methyl-3,5-diphenyl-1H-pyrazole

https://huagongshe.com/reaction/441532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
ReactantSodium HydroxideHCID 14798—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant1-Methyl-3,5-diphenyl-4-(phenylsulfanyl)-1H-pyrazoleHCID 21398055—
SolventChloroformHCID 6212—
Product4-(Benzenesulfonyl)-1-methyl-3,5-diphenyl-1H-pyrazoleHCID 2139808391%

Reaction Conditions

Temperature9 °C

Reaction Steps

At a temperature of 9° C. a solution of m-chloroperbenzoic acid (10.15 g, 85%, 0.05 mole) in dry chloroform (50 ml) is added to a solution of 4-(phenylthio)-1-methyl-3,5-diphenylpyrazole (6.84 g, 0.02 mole) in dry chloroform (50 ml). The reaction mixture is stirred for 3 hours at 9° C. and then overnight at room temperature. A heavy precipitate forms. The mixture is treated with 2% aqueous sodium hydroxide and extracted with chloroform. The chloroform layer is separated and stripped in vacuo to give an oil. Trituration of the oil with cyclohexane affords crystals 6.8 g (91%), m.p. 135° C. to 141° C. Recrystallization from a mixture of benzene and pentane gave white crystals, m.p. 149° C. to 150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04041046
Source datasetuspto-grants-1977_08
ORD IDord-1bde99e2c402426f9669eb5d0280560b
Source noteuspto-grants-1977_08