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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 260342Erstellt: 24. Oktober 2026

Benzene, (2-chloroethoxy)- → 2-(4-Chlorophenyl)-4-phenoxybutanenitrile

https://huagongshe.com/de/reaction/260342

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, (2-chloroethoxy)-HCID 12156—
EduktSodium hydrideHCID 24758—
Edukt4-Chlorobenzyl cyanideHCID 241582—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(4-Chlorophenyl)-4-phenoxybutanenitrileHCID 2240143496%

Reaktionsschritte

To a flask was added 7.2 g. (0.150 mole) of a 50% oil dispersion of sodium hydride. After washing the sodium hydride several times with hexane to remove the mineral oil, 18.9 g. (0.125 mole) of 4-chlorobenzyl cyanide in 50 ml of dry DMF was added dropwise at 0° C. Upon completion of the addition, the reaction was stirred for one hour while warming to room temperature, then 20.0 g. (0.128 mole) of 1-chloro-2-phenoxyethane was added dropwise at 15° C. over a 30 minute period. The stirred reaction was allowed to warm to room temperature and was complete in two hours. The reaction mixture was diluted with 300 ml. of water and extracted three times with 100 ml. portions of methylene chloride. The combined extracts were washed with dilute hydrochloric acid and water followed by drying using sodium sulfate. Upon removal of the solvent, 33 g. of the crude 2-(4-chlorophenyl)-4-phenoxybutanenitrile was obtained (96% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05527816
Quelldatensatzuspto-grants-1996_06
ORD IDord-8c84c1bffeec4cccbbb4be07a6dc021c
Quellennotizuspto-grants-1996_06