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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727743Generated: October 31, 2026

Methyl iodide → HCID 15735343, compound

https://huagongshe.com/reaction/727743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-nitroanisoleHCID 2779250—
ReactantHCID 19824395HCID 19824395—
ReactantButyllithiumHCID 178418339—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15735343HCID 15735343—

Reaction Steps

To a solution of 15.4 g (45.16 mmol) of 5-difluoromethyl-4-bromo-3-(bismethyl-t-butylsiloxy)-1-methylpyrazole in anhydrous THF was added 18.06 ml of 2.5 molar n-butyl lithium at -78° C. The mixture was stirred for 1 hour with methyl iodide and warmed to room temperature. Ether was added and the ether layer was washed with water, dried and evaporated to give an oily residue. The residue was dissolved in 100 ml of acetonitrile and 5 ml of concentrated aqueous HF added to precipitate 2.8 g of a white solid mp 145°-146° C. (b) A mixture of 1.0 g of the product of step (a) (6.17 mmol), 4-fluoro-2-methoxynitrobenzene (1.06 g 6.17 mmol), and 0.94 g of potassium carbonate (6.79 mmol) in 50 ml dimethyl sulfoxide was heated to 80° C. for 15 hours. The reaction was then poured into 200 ml cold water and stirred for 1-2 hours. The precipitate formed was collected to give 1.8 g of a white solid product m.p. 57°-58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045106
Source datasetuspto-grants-1991_09
ORD IDord-bb25413072b44e99bf205dcb2518f9b8
Source noteuspto-grants-1991_09