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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3966Erstellt: 24. Oktober 2026

1,4-Difluorobenzene → 1-Acetyl-4-(2,5-difluorobenzoyl)piperidine

https://huagongshe.com/de/reaction/3966

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DifluorobenzeneHCID 10892—
Edukt1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
EduktAluminum(III) ChlorideHCID 6451240—
Produkt1-Acetyl-4-(2,5-difluorobenzoyl)piperidineHCID 1380013152,1%

Reaktionsschritte

To a stirred suspension of 100 g of 1-acetyl-4-piperidine carboxylic acid chloride in 500 ml of 1,4-difluorobenzene was added in aliquots, 211 g of anhydrous aluminum chloride. The mixture was stirred at reflux under nitrogen for 3 hrs and allowed to cool to room temperature. The mixture was poured into ice and extracted twice with ethyl acetate. The extracts were washed with saturated sodium bicarbonate solution and dried over anhydrous potassium carbonate. Filtration followed by evaporation of the solvent provided an oil which crystallized on standing. The solid was washed with cyclohexane and dried to provide 73.3 g (52.1%) of 1-acetyl-4-(2,5-difluorobenzoyl)piperidine: mp 82°-87° C. Recrystallization from a mixture of isopropyl alcohol, diisopropyl ether and hexane provided product with mp 93°-95° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04723009
Quelldatensatzuspto-grants-1988_02
ORD IDord-8b653410a1d44cdf9990edd4a831a13b
Quellennotizuspto-grants-1988_02