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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-2-ethynylbenzene | HCID 585995 | — |
| Reactant | 3-Chloro-5-(3,3-dichloroprop-2-enyloxy)-1-iodo-2-[3-(5-trifluoromethylpyrid-2-yloxy)propyloxy]benzene | HCID 22318611 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-Chloro-3-(2-chlorophenylethynyl)-5-(3,3-dichloroprop-2-enyloxy)-2-[3-(5-trifluoromethylpyrid-2-yloxy)propyloxy]benzene | HCID 22318621 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06949551B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-92a23c6079f7404a99fb005e93533f0d |
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| Source note | uspto-grants-2005_09 |
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