戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 3966作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DifluorobenzeneHCID 10892—
反応物1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
反応物Aluminum(III) ChlorideHCID 6451240—
生成物1-Acetyl-4-(2,5-difluorobenzoyl)piperidineHCID 1380013152.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04723009
出典データセットuspto-grants-1988_02
ORD IDord-8b653410a1d44cdf9990edd4a831a13b
出典メモuspto-grants-1988_02