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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 260343Erstellt: 25. Oktober 2026

Dibromomethane → 1-Bromo-2-(4-chlorophenyl)-2-cyano-4-phenoxybutane

https://huagongshe.com/reaction/260343

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDibromomethaneHCID 3024—
EduktSodium hydrideHCID 24758—
Edukt2-(4-Chlorophenyl)-4-phenoxybutanenitrileHCID 22401434—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Bromo-2-(4-chlorophenyl)-2-cyano-4-phenoxybutaneHCID 1533460477%

Reaktionsschritte

To a flask was added 6.1 g. (0.127 mole) of a 50% oil dispersion of sodium hydride. After washing the sodium hydride several times with hexane to remove the mineral oil, 50 ml. of dry DMF was added, then a solution of 30 g. (0.11 mole) of 2-(4-chlorophenyl)-4-phenoxybutanenitrile in 25 ml. of dry DMF was added dropwise at 0° C. The reaction was stirred and allowed to warm to room temperature over 1.5 hours, then 21.2 g. (0.127 mole) of dibromomethane was added dropwise at 15° C. Upon completion of the addition, the reaction was stirred and heated to 50° C. and was complete in three hours. The reaction mixture was cooled to room temperature, diluted with 300 ml. of water, and then extracted three times with 100 ml. portions of methylene chloride. The combined extracts were washed with dilute hydrochloric acid and water, then dried using sodium sulfate. Upon removal of the solvent, 31 g. of 1-bromo-2-(4-chlorophenyl)-2-cyano-4-phenoxybutane was obtained (77% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05527816
Quelldatensatzuspto-grants-1996_06
ORD IDord-c47a7f519ea7492da93eda1ced67b7bd
Quellennotizuspto-grants-1996_06