Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 482290Erstellt: 24. Oktober 2026

Chloropyrazine → Pyrazine, 2-phenyl-

https://huagongshe.com/de/reaction/482290

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloropyrazineHCID 73277—
EduktHCID 178418255HCID 178418255—
Katalysator[1,2-Bis(diphenylphosphino)ethane]dichloronickel(II)HCID 2734542—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktPyrazine, 2-phenyl-HCID 64287039%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05795894
Quelldatensatzuspto-grants-1998_08
ORD IDord-ba32755abd7c420a9096422057f19698
Quellennotizuspto-grants-1998_08