HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963010Generated: October 30, 2026
Ethyl 4-ethynylbenzoate → HCID 56987556, compound
https://huagongshe.com/reaction/963010
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-ethynylbenzoate | HCID 15540683 | — |
| 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 56987556 | HCID 56987556 | — |
Reaction Steps
A solution of 2-(2-iodoethenyl)-3-methyl-2-cyclohexen-1-one (Compound 4, 1.74 g, 6.64 mmol), ethyl 4-ethynylbenzoate (1.73 g, 9.96 mmol) and triethylamine (80 mL) was purged with argon for 10 minutes, and then treated with bis(triphenylphosphine)palladium (II) chloride (23 mg, 0.03 mmol) and copper (I) iodide (6.3 mg, 0.03 mmol). The solution was stirred 40° C. for 3 hours, and concentrated under the vacuum of a water aspirator. The residue was dissolved in ethyl acetate and washed with saturated aqueous NH4Cl. The layers were separated and the aqueous layer was extracted 2× 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 (88:12, hexane:ethyl acetate) to give the title compound as a yellow crystaline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05760276 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-6d82e1a984894aa6becf26afdc725f8c |
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| Source note | uspto-grants-1998_06 |
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