Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Hexyne | HCID 12732 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Catalyst | Palladium, di-mu-chlorobis(eta3-2-propenyl)di- | HCID 61538 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | 1,3-Di(tricyclo[3.3.1.1~3,7~]decan-1-yl)-1H-imidazol-3-ium chloride | HCID 2734915 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 55269048 | HCID 55269048 | 73% |
Reaction Steps
1-Hexyne (43 μl, 0.38 mmol) and ethyl 4-bromobutyrate (40 μl, 0.28 mmol) were added to a suspension of 1,3-bis(1-adamantyl)imidazolium chloride (5.2 mg, 0.014 mmol), copper iodide (4.1 mg, 0.022 mmol), allylpalladium(II) chloride dimer (2.6 mg, 0.071 mmol) and cesium carbonate (127 mg, 0.390 mmol) in anhydrous ether (0.37 ml)-anhydrous DMF (0.185 ml) at room temperature in a nitrogen stream, and the mixture was stirred at 45° C. for 17 hours. The reaction mixture was extracted with pentane. The insoluble matter was removed by filtration, and the filtrate was then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ether=50/1) to give dec-5-ynoic acid ethyl ester (40 mg, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169254B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-a8f6768d3ff54bb2a2fb74cd297f04c9 |
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| Source note | uspto-grants-2015_10 |
|---|