Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274322Generated: November 1, 2026

Diethyl Ether → HCID 22120914, compound

https://huagongshe.com/reaction/1274322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Amino-3-cyano-4-iodo-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]pyrazoleHCID 15462077—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 22120914HCID 22120914—

Reaction Steps

To a rapidly stirred solution of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-iodopyrazole (0.447 g) in toluene (2 ml) containing tetrakis(triphenylphosphine)palladium(0) (0.02 g) was added saturated aqueous sodium hydrogen carbonate solution (1 ml) and a solution of 4-methoxyphenylboronic acid (0.302 g) in ethanol (1 ml). The mixture was heated under reflux for 2.75 hours, then left at room temperature overnight. Saturated aqueous sodium hydrogen carbonate solution (0.5 ml) and tetrakis(triphenylphosphine)palladium(0) (0.01 g) were added and the mixture heated under reflux for 3 hours. The cooled reaction mixture was then poured into ether (25 ml) and water (25 ml). The organic layer was separated, dried (MgSO4) and evaporated. The residue was purified by column chromatography on silica gel (50 g) eluted with dichloromethane. Combination and evaporation of suitable fractions gave the title compound as an off-white crystalline solid, m.p. 222° C. with softening at 192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156782
Source datasetuspto-grants-2000_12
ORD IDord-69c5a282aacb4a21b7d7e05c62c2a3d4
Source noteuspto-grants-2000_12