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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231122Erstellt: 23. Oktober 2026

1,3-Difluorobenzene → 4-Chloro-1-(2,4-difluorophenyl)butan-1-one

https://huagongshe.com/de/reaction/231122

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-DifluorobenzeneHCID 9741—
Edukt4-Chlorobutyryl chlorideHCID 78370—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Chloro-1-(2,4-difluorophenyl)butan-1-oneHCID 1033101085,2%

Reaktionsschritte

255 g (1.81 mols) of 4-chlorobutyryl chloride are added dropwise to a mixture of 200 g (1.75 mols) of 1,3-difluorobenzene and 256 g (1.92 mols) of anhydrous aluminum chloride at room temperature, while stirring. The mixture is stirred at 30° C. for 4 hours and then poured onto 1,200 g of ice. 1,200 ml of methylene chloride are added, the organic phase is separated off, the aqueous phase is extracted with methylene chloride and the combined organic phases are washed with water, dried over sodium sulphate and concentrated by stripping off the solvent under reduced pressure. The residue which remains is distilled. 326 g (85% of theory) of 2,4-difluorophenyl 3-chloropropyl ketone are obtained in this manner.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04845116
Quelldatensatzuspto-grants-1989_07
ORD IDord-c62facb23d654e3e81f07915e4d8f847
Quellennotizuspto-grants-1989_07