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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497054Generated: November 2, 2026

1-Chloro-2-ethynylbenzene → 1-Chloro-3-(2-chlorophenylethynyl)-5-(3,3-dichloroprop-2-enyloxy)-2-[3-(5-trifluoromethylpyrid-2-yloxy)propyloxy]benzene

https://huagongshe.com/reaction/497054

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-ethynylbenzeneHCID 585995—
Reactant3-Chloro-5-(3,3-dichloroprop-2-enyloxy)-1-iodo-2-[3-(5-trifluoromethylpyrid-2-yloxy)propyloxy]benzeneHCID 22318611—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product1-Chloro-3-(2-chlorophenylethynyl)-5-(3,3-dichloroprop-2-enyloxy)-2-[3-(5-trifluoromethylpyrid-2-yloxy)propyloxy]benzeneHCID 22318621—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under an atmosphere of protective gas, 0.1 g of 3-chloro-5-(3,3-dichloroprop-2-enyloxy)-1-iodo-2-[3-(5-trifluoromethylpyrid-2-yloxy)propyloxy]benzene, 0.03 g of 1-chloro-2-ethynylbenzene and 0.003 g of copper(I) iodide were dissolved in 1 ml of triethylamine. 0.005 g of bis(triphenylphosphine)palladium(II) chloride was added, and the mixture was stirred at 70° C. for 1 hour. The mixture was then allowed to cool and concentrated under reduced pressure, and the resulting residue was subjected to chromatographic purification. Yield: 0.085 g (84%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949551B2
Source datasetuspto-grants-2005_09
ORD IDord-92a23c6079f7404a99fb005e93533f0d
Source noteuspto-grants-2005_09