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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598512Generated: November 4, 2026

Methyl iodide → 3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfenylpyrazole

https://huagongshe.com/reaction/1598512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178481742HCID 178481742—
SolventAcetonitrileHCID 6342—
Product3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfenylpyrazoleHCID 1892941997.8%

Reaction Steps

A suspension of 0.5 g of 3-(2,6-dichloro-4-trifluoromethylphenyl)-5-mercapto-1-methylpyrazole (2), 2.3 g of methyl iodide and 0.4 g of anhydrous potassium carbonate in 10 ml of acetonitrile was refluxed overnight with stirring. The reaction mixture was cooled to room temperature and filtered through Celite, and the filtrate was concentrated under reduced pressure. The residue was purified by chromatography on silica gel to obtain 0.51 g of the desired product in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739083
Source datasetuspto-grants-1998_04
ORD IDord-d64ec6771ae04d188fa3214f745faab4
Source noteuspto-grants-1998_04