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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762747Generated: October 26, 2026

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

https://huagongshe.com/reaction/1762747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DifluorobenzeneHCID 10892—
Reactant1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
ReactantAluminum(III) ChlorideHCID 6451240—
Product1-Acetyl-4-(2,5-difluorobenzoyl)piperidineHCID 1380013152.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04833244
Source datasetuspto-grants-1989_05
ORD IDord-6e359f1e3ea74139a7bf5a9c2f973868
Source noteuspto-grants-1989_05