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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1701735Erstellt: 25. Oktober 2026

Allyl Alcohol → 4-{3-[(Prop-2-en-1-yl)oxy]pyrazin-2-yl}morpholine

https://huagongshe.com/reaction/1701735

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl AlcoholHCID 7858—
EduktSodium hydrideHCID 24758—
Edukt4-(3-Chloropyrazin-2-YL)morpholineHCID 20528994—
LösungsmittelHexamethylphosphoramideHCID 12679—
Produkt4-{3-[(Prop-2-en-1-yl)oxy]pyrazin-2-yl}morpholineHCID 57067635—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

120 g of 2-chloro-3-morpholinyl-pyrazine and 70 g of allyl alcohol are dissolved in 640 ml of hexamethylphosphoric acid triamide. 28.8 g of sodium hydride are introduced into this solution over the course of 30 minutes at 0° C. The mixture is then stirred for a further hour at 0° C. and thereafter for 1 hour at 30° C. and 15 hours at room temperature, until the reaction has subsided. The reaction mixture is then poured out onto 2 liters of ice water. After the excess sodium hydride present has been decomposed, the mixture is extracted by shaking with ether. The ether extracts are washed with water until neutral, dried over sodium sulphate and evaporated in a waterpump vacuum. The residue is distilled in a high vacuum. 2-Allyloxy-3-morpholinyl-pyrazine, boiling point 105°-106° C./0.03 mm Hg, is thus obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04195090
Quelldatensatzuspto-grants-1980_03
ORD IDord-4a7d77d451de4beb854b52acf32445a8
Quellennotizuspto-grants-1980_03