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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 613792Erstellt: 25. Oktober 2026

Water → 4,4'-((R)-1-methylpropanedioxy)bisbenzonitrile

https://huagongshe.com/reaction/613792

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-ChlorobenzonitrileHCID 12163—
EduktSodium hydrideHCID 24758—
Edukt(-)-1,3-ButanediolHCID 637497—
LösungsmittelDimethylformamideHCID 6228—
Produkt4,4'-((R)-1-methylpropanedioxy)bisbenzonitrileHCID 6758549681,4%

Reaktionsschritte

Sodium hydride (3.18 g, 133 mmol) was dispersed in 100 ml DMF and added with 1,3-(R)-butanediol (5.03 g, 55.8 mmol) while being cooled with ice. The mixture after being cooled with ice for another one hour was stirred at room temperature for 2 hours and then added with 4-chlorobenzonitrile (16.8 g, 122 mmol) at room temperature, followed by being reacted for 20 hours. After completion of the reaction, the reaction mixture was carefully added with 5 ml water to inactivate excess sodium hydride, followed by distilling out DMF in vacuum. The resulting mixture after being added with 200 ml of water was subjected to processes of extraction of an organic matter with ethyl acetate, washing with a solution of saturated sodium chloride and distillation of the solvent, followed by distillation of the oily residue thus obtained using Kugelloa distilling equipment at a temperature of 275° C. and a pressure of 0.5 mmHg thereby obtaining the intended product (13.3 g, 45.4 mmol, 81%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06008401
Quelldatensatzuspto-grants-1999_12
ORD IDord-8b56f25dd26b46b69a4c77123d3e6ed5
Quellennotizuspto-grants-1999_12