HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369441Generated: October 30, 2026
Cyclopropylacetylene → HCID 69670549, compound
https://huagongshe.com/reaction/2369441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropylacetylene | HCID 138823 | — |
| Reactant | HCID 69670677 | HCID 69670677 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 69670549 | HCID 69670549 | 78% |
Reaction Steps
Bis(triphenylphosphine)palladium(II) dichloride ([(C6H5)3P]2PdCl2, 0.0518 g, 5 mol %), copper(I) iodide (0.0086 g, 3 mol %), and triethylamine (3 ml) were charged into a 25-ml round-bottomed flask equipped with a stirrer, and were suspended by stirring at room temperature. To the suspension, a solution obtained by dissolving 2-trifluoromethylsulfanyliodobenzene (1.08 g, 3.6 mmol) prepared in Reference Example 1 and cyclopropylacetylene (0.35 g, 5.3 mmol) in triethylamine (2 ml) was added dropwise, and the solution was stirred at room temperature overnight. After completion of the reaction, a solvent was removed under reduced pressure, and water was added to the obtained residue. The solution was extracted with ether, and the organic layers were combined together, washed with water, dried over magnesium sulfate, filtered, and concentrated to obtain a crude product. The obtained crude product was purified by silica gel column chromatography (hexane) to give target 1-cyclopropylethynyl-2-trifluoromethylsulfanylbenzene (0.67 g, yield: 78%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703969B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-2c273257a884400bb5cdbf5ff86f349f |
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| Source note | uspto-grants-2014_04 |
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