HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991864Generated: October 31, 2026
HCID 11299597, compound → HCID 57027195, compound
https://huagongshe.com/reaction/991864
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 11299597 | HCID 11299597 | — |
| Reactant | HCID 57287130 | HCID 57287130 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 57027195 | HCID 57027195 | — |
Reaction Steps
A solution of 1-iodo-2-(2-methyl-6-oxocyclohex-1-enyl)ethene (Compound E, available in accordance with the teachings of U.S. Pat. No. 5,760,276, 0.70 g, 2.67 mmol), (trimethylsilyl)ethyl 4-ethynylbenzoate (Compound C, 0.79 g, 3.21 mmol) and triethylamine (32 ml) was purged with argon for 10 minutes, and then treated with bis(triphenylphosphine)palladium (II) chloride (47 mg, 0.07 mmol) and copper (I) iodide (12.8 mg, 0.07 mmol). The solution was stirred 40° C. for 3 hours, and concentrated under a water aspirator vacuum. The residue was dissolved in ethyl acetate and washed with saturated aqueous NH4Cl. The layers were separated and the aqueous layer was extracted twice with ethyl acetate. The combined organic fractions were washed with water, and brine, and dried (MgSO4). The solvents were removed under reduced pressure, and the residue was purified by silica gel chromatography (90:10, hexane:ethyl acetate) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06465646B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-8b7e5ba01d2c45b683cbfd619b8d77b9 |
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| Source note | uspto-grants-2002_10 |
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