Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloropyrazine | HCID 73277 | — |
| Edukt | HCID 178418255 | HCID 178418255 | — |
| Katalysator | [1,2-Bis(diphenylphosphino)ethane]dichloronickel(II) | HCID 2734542 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Pyrazine, 2-phenyl- | HCID 642870 | 39% |
Reaktionsschritte
Chloropyrazine (20.68 gram, 177 mmol) and [1,2-bis(diphenylphosphino)ethane]nickel(II) chloride (41.08 gram, 77.8 mmol) in dry THF (1.5 liter) were mixed and stirred for 80 minutes in a flask (cooled with a water bath) under nitrogen. A solution of phenylmagnesium bromide (3M in Et2O) (103 ml, 309 mmol) was added slowly through a dropping funnel into the cooled brick-red slurry at room temperature under nitrogen over 3.5 hours. After stirring at room temperature overnight, TLC showed that the reaction was complete. 3 N HCI (100 ml) was added slowly through a dropping funnel under nitrogen and the mixture was stirred for one hour. The THF layer was separated from the aqueous layer. The aqueous layer was adjusted to pH 12 with 6 N NaOH and extracted with EtOAc (100 ml, 3×). The organic fractions (THF and EtOAc) were combined and dried over MgSO4, filtered and concentrated to give a solid. The product was purified by flash chromatography on 300 g of flash grade silica gel in 2.5% EtOAc/CH2Cl2 to give 10.79 gram (69 mmol, 39%) of 2-phenylpyrazine, m.p. 69°-70° C.; FAB mass [M+1]+ 157;
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05795894 |
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| Quelldatensatz | uspto-grants-1998_08 |
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| ORD ID | ord-ba32755abd7c420a9096422057f19698 |
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| Quellennotiz | uspto-grants-1998_08 |
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