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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 392361Erstellt: 25. Oktober 2026

Ethyl Acetate → HCID 22662796, Verbindung

https://huagongshe.com/reaction/392361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt18-Crown-6HCID 28557—
Edukt6-Chloropyrazine-2-carbonitrileHCID 81303—
EduktPotassium FluorideHCID 522689—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 22662796HCID 2266279649,3%

Reaktionsschritte

In a mixture of 140 ml of acetonitrile and 280 ml of toluene were suspended 58 g of potassium fluoride (spray-dried) and 8.7 g f 18-crown-6-ether. After heating the suspension under reflux for one hour in an atmosphere of nitrogen gas, the acetonitrile and toluene were distilled off under atmospheric pressure. The residue thus obtained was suspended in 280 mL of acetonitrile, 23 g of 6-chloro-2-pyrazinecarbonitrile synthesized according to the method described in Acta Poloniae Pharmaceutica, Vol. 33, Pages 153-161 (1976) was added, and the mixture thus obtained was heated under reflux for one hour in an atmosphere of nitrogen. The reaction mixture was cooled to room temperature, 280 mL of ethyl acetate and 280 mL of water were added, and the organic layer was separated. The organic layer thus obtained was washed successively with water and saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was distilled off under a reduce pressure. The residue was purified by silica gel column chromatography [eluent: n-hexane:ethyl acetate=10:1] to obtain 10 g of 6-fluoro-2-pyrazinecarbonitrile as a white-colored solid product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06800629B2
Quelldatensatzuspto-grants-2004_10
ORD IDord-5c6ed00921bc476eb4b71e438687f8ad
Quellennotizuspto-grants-2004_10