Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Edukt | 4-Cyanophenylboronic acid | HCID 2734326 | — |
| Edukt | 5-Bromo-2-ethenyl-1,3-benzoxazole | HCID 21980099 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 4-(2-Vinyl-benzooxazol-5-yl)-benzonitrile | HCID 21980091 | 78% |
Reaktionsschritte
A mixture of 224 mg (1 mmol) of 5-bromo-2-vinyl-benzooxazole, 191 mg (1.3 mmol) of 4-cyanophenylboronic acid, 55 mg (0.03 mmol) of tris-(dibenzylidineacetone)dipalladium (0) (CAS #52409-22-0), 0.2 mL (0.06 mmol) of a 10% solution of tri-tert-butylphosphine in hexane, and 1.5 mL of tetrahydrofuran was stirred at 23° C. for 24 hours. It was then heated at 65° C. for 0.5 hour, then cooled. The mixture was suction filtered to remove particulates, then partitioned between 80 mL of water and a mixture of 30 mL of ethyl acetate and 10 mL of hexane. The organic phase was collected, dried over Na2SO4, and purified by flash chromatography on silica gel (eluting with 1:1 hexane: dichloromethane) to give 4-(2-vinyl-benzooxazol-5-yl)-benzonitrile (192 mg, 78%) as a white solid: mp 143-144° C.;
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08106088B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-fdee3ae3e70641eda44083ba7aa8aeb1 |
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| Quellennotiz | uspto-grants-2012_01 |
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