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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231561Erstellt: 24. Oktober 2026

Dichloromethane → 3-Cyanomethyl-1-(4-fluorophenyl)-pyrrolidine-2,5-dione

https://huagongshe.com/de/reaction/231561

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktPotassium CyanideHCID 9032—
Edukt3-Chloromethyl-1-(4-fluorophenyl)-pyrrolidine-2,5-dioneHCID 20033479—
KatalysatorHexadecyltrimethylammonium chlorideHCID 8154—
LösungsmittelWaterHCID 962—
Produkt3-Cyanomethyl-1-(4-fluorophenyl)-pyrrolidine-2,5-dioneHCID 2003347344,1%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

A mixture was prepared of 48.3 g (0.2 moles) 3-chloromethyl-1-(4-fluorophenyl)-pyrrolidine-2,5-dione (according to Example 1), 300 ml methylene chloride and 7 g hexadecyltrimethylammonium chloride, dissolved in 80 ml water. To this mixture, a solution of 28.6 g (0.43 moles) potassium cyanide in 90 ml water was added dropwise at 0° C., and then stirred for 4 hours at 0° C. and another 12 hours at 20° C. The resulting phases were then separated with the organic phase being washed with water and dried with sodium sulfate. Finally, methylene chloride was distilled off and the residue dissolved in 250 ml toluene. Upon standing, the desired product crystallized. The actual yield was 44.1% of the theoretical yield. Melting point 97° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04847285
Quelldatensatzuspto-grants-1989_07
ORD IDord-d6e02fc7af094cef97031a1bcfd16e46
Quellennotizuspto-grants-1989_07