HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727190Generated: October 30, 2026
Triethylamine → 4-[3,5-Di(trifluoromethyl)phenylethynyl]cyclohexanone
https://huagongshe.com/reaction/727190
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Iodo-3,5-bis(trifluoromethyl)benzene | HCID 630970 | — |
| Reactant | 8-Ethynyl-1,4-dioxaspiro[4.5]decane | HCID 19705273 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[3,5-Di(trifluoromethyl)phenylethynyl]cyclohexanone | HCID 19705254 | — |
Reaction Steps
A solution of 3.9 grams (0.022 mole) of 8-ethynyl-1,4-dioxaspiro[4.5]decane, 10.5 grams (0.031 mole) of 3,5-di(trifluoromethyl)phenyl iodide (prepared in Step A of this Example), 10.7 grams (0.077 mole) of triethylamine, 0.5 gram (catalyst) of bis(triphenylphosphine)palladium(II) chloride, and 0.5 gram (catalyst) of copper(I) iodide in 100 mL of acetonitrile is stirred at ambient temperature for about 18 hours. After this time the reaction mixture is concentrated under reduced pressure to a residue. The residue is then stirred for about 2 hours with 150 mL of aqueous 1N hydrochloric acid. After this time the mixture is extracted with three 100 mL portions of ethyl acetate. The combined extracts are washed with an aqueous solution of 10% lithium chloride. The organic layer is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure, yielding 4-[3,5-di(trifluoromethyl)phenylethynyl]cyclohexanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05712281 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-490946760c004400add7ed9f518badf6 |
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| Source note | uspto-grants-1998_01 |
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