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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274331Generated: October 29, 2026

Diethyl Ether → HCID 9955245, compound

https://huagongshe.com/reaction/1274331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant1-Naphthaleneboronic acidHCID 254532—
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 9955245HCID 9955245—

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 1-naphthylboronic acid (0.344 g) in ethanol (1 ml). The mixture was heated under reflux for 3 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 layers were separated and the aqueous phase extracted with a second portion of ether (25 ml). The combined organic layers were washed with water (2×25 ml), brine (25 ml) and then 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. 208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156782
Source datasetuspto-grants-2000_12
ORD IDord-8a7b1bfc0ab64d1098ce68d8125c79f3
Source noteuspto-grants-2000_12