Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | HCID 12709354 | HCID 12709354 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Bis(benzonitrile)palladium chloride | HCID 498840 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10378725 | HCID 10378725 | 72% |
Reaction Steps
1,4-Dioxane (2.5 mL, dry) was added to a stirred suspension of CuI (8.0 mg, 2 mol %) and dichlorobis(benzonitrile)palladium (II) (24 mg, 3 mol %) in a dry septum-capped flask with constant purging of argon. Tri-t-butylphosphine (542 μl, 0.25M solution in 1,4-dioxane), diisopropyl amine (350 μl, 4.17 mmol), acetic acid 2-bromo-4-cyano-phenyl ester (500 mg, 2.08 mmol), and phenyl acetylene (254 mg, 2.71 mmol) were added with syringes to the stirred reaction mixture. The reaction mixture was stirred for 6 hours, and then diluted with ethyl acetate and passed through small pad of silica gel. The filtrate was concentrated, and the crude product was purified by column chromatography (silica gel, 5 to 20% ethyl acetate in hexanes) to provide 390 mg (72%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666863B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-8ef4f2af0ab54fecb7d756dece94d336 |
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| Source note | uspto-grants-2010_02 |
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