Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670368Generated: October 31, 2026

Methyl iodide → 1-Methyl-5-methylthio-3-(trifluoromethyl)pyrazole

https://huagongshe.com/reaction/1670368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methyl-5-trifluoromethyl-2H-pyrazole-3-thiolHCID 19067687—
SolventAcetonitrileHCID 6342—
Product1-Methyl-5-methylthio-3-(trifluoromethyl)pyrazoleHCID 5935638486.4%

Reaction Steps

3.87 g of compound (8-5) and 4.40 g of potassium carbonate were suspended in 100 ml of acetonitrile. The suspension was stirred at room temperature for 15 minutes. A solution of 3.62 g of methyl iodide in 10 ml of acetonitrile was added dropwise, and the mixture was stirred at room temperature for 12 hours. The reaction solution was concentrated under reduced pressure. After water was added to the residue, the mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure to produce 3.60 g of 1-methyl-5-methylthio-3-(trifluoromethyl)pyrazole (14).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994094B2
Source datasetuspto-grants-2011_08
ORD IDord-8e735db6e981406bb4caae1efa0c81d8
Source noteuspto-grants-2011_08