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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532579Generated: October 27, 2026

Iodine → 3-(3-Fluoro-5-chloro-2-pyridyl)-4-iodo-5-difluoromethoxy-1-methyl-[1H]-pyrazole

https://huagongshe.com/reaction/1532579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant3-(3-fluoro-5chloro-2-pyridyl)-5-difluoromethoxy-1-methyl-[1H]-pyrazoleHCID 21712132—
CatalystSilver nitriteHCID 160904—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product3-(3-Fluoro-5-chloro-2-pyridyl)-4-iodo-5-difluoromethoxy-1-methyl-[1H]-pyrazoleHCID 2201357991%

Reaction Conditions

Temperature22 °C

Reaction Steps

3.0 g of 3-(3-fluoro-5-chloro-2-pyridyl)-5-difluoromethoxy-1-methyl-[1H]-pyrazole (Example H15) are dissolved in 30 ml of methylene chloride, and 1.83 g of silver(I) nitrite and 3.02 g of iodine are then added. The mixture is stirred overnight at 22° C. It is then diluted with diethyl ether and extracted successively with aqueous sodium metabisulfite solution and brine. After drying of the organic phase over sodium sulfate and filtration, the filtrate is concentrated in vacuo together with twice the amount of silica gel. After application of this silica gel to a flash column, the column is eluted with n-hexane/ethyl acetate (3/1). 3.97 g of the desired title compound are obtained as a beige solid of melting point 77-78° C. in this manner.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204221B1
Source datasetuspto-grants-2001_03
ORD IDord-30c05a42368142c3b41bdb27ae10dfb3
Source noteuspto-grants-2001_03