Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Tridecane | HCID 12388 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Diphenylacetylene | HCID 10390 | 44% |
Reaction Steps
A solution of phenylacetylene (0.439 ml; 0.409 g; 4.00 mmol) in THF (2 ml) was treated at 0° C. with n-butyllithium (1.6 ml; 4.0 mmol; 2.5 M in hexanes) and the resulting solution was allowed to warm to room temperature for 10 min. The solution was cooled to 0° C., then treated with a solution of ZnBr2 (0.923 g; 4.10 mmol) in THF (2 ml) and allowed to warm to room temperature for 30 min. Solvent was removed in vacuo, then 1,4-dioxane (2 ml) was added. This solution was then added to a room temperature solution of benzonitrile (0.204 ml; 0.206 g; 2.00 mmol), dichlorobis(trimethylphosphine)nickel (0.0564 g; 10 mol %), and tridecane (0.244 ml; 0.184 g; 1.00 mmol) in 1,4-dioxane (2 ml). The reaction mixture was then heated to 65° C. and stirred for 42 h; then a sample was withdrawn and quenched in a mixture of 1 M sodium citrate (aq) and MTBE. GC analysis of the organic phase of the hydrolyzed reaction sample showed the presence of 0.88 mmol (44% yield) of diphenylacetylene and 0.51 mmol of benzonitrile remaining in the reaction mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105707B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-e6e47685793f4076961a5973d8d4b863 |
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| Source note | uspto-grants-2006_09 |
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