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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 549069Erstellt: 26. Oktober 2026

Allyl bromide → Pyrazine, 3-butenyl-

https://huagongshe.com/reaction/549069

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktDiisopropylamineHCID 7912—
Edukt2-MethylpyrazineHCID 7976—
EduktAmmonium ChlorideHCID 25517—
EduktLithium diisopropylamineHCID 45051747—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktPyrazine, 3-butenyl-HCID 22477625—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

A solution of lithium diisopropylamine [prepared from a solution of butyl lithium in hexanes (100 mL, 2.5M) and diisopropylamine (25.3 g) at −35° C.] was treated with a solution of 2-methylpyrazine (23.5 g) in dry tetrahydrofuran (300 mL) at −20° C. The mixture was stirred at −20° C. for 1 hour then cooled to −78° C. and treated with a solution of allyl bromide (30.8 g) in dry tetrahydrofuran (300 mL). This mixture was warmed to room temperature and stirred at this temperature for 2 hours then left overnight and then treated with saturated ammonium chloride solution (50 mL) followed by water (200 mL). The mixture was then extracted twice with ether (200 mL). The combined extracts were dried over magnesium sulfate then evaporated. The residue was distilled to give the title compound (22 g) as a colourless oil, b.p. 70° C./1 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943616B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-4815e54b89fa4163900dcedc3ced0e59
Quellennotizuspto-grants-2011_05