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化工社化工社 化学情報印刷レポート · 研究参考用
HRID 895791作成日:2026年10月26日

Sulfuric Acid → 1-Benzyl-4-phenylpiperidine-4-carboxamide

https://huagongshe.com/reaction/895791

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Sodium HydroxideHCID 14798—
反応物1-Benzyl-4-cyano-4-phenylpiperidineHCID 191408—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物1-Benzyl-4-phenylpiperidine-4-carboxamideHCID 9642395%

反応条件

温度60 °C

反応手順

A mixture of 3 kg of commercial 1-benzyl-4-cyano-4-phenylpiperidine, 6 l of water, 8.98 l of toluene and 1.35 kg of an aqueous 35% sodium hydroxide solution is heated under nitrogen at 60° C. and the aqueous phase is separated out by settling at this temperature. The toluene phase is dried by azeotropic distillation and the solution thus obtained containing the 1-benzyl-4-cyano-4-phenylpiperidine base is added to a mixture of 2.83 kg of 95% sulfuric acid, 1.73 kg of glacial acetic acid and 3 l of toluene. The mixture thus obtained is heated for 6 hours, the heating is then stopped, the mixture is cooled to 60° C. and 3 l of water are added at this temperature. The mixture is allowed to cool to room temperature (about 20° C.) and is then poured into 8.65 l of 30% sodium hydroxide and 6.75 l of water. The temperature rises gradually to 75° C. The phases are separated by settling while hot and the organic phase is washed with water and dried azeotropically. The toluene solution is concentrated to half its volume and then cooled gradually to 60° C. and the crystallization is initiated. The crystallization is completed by cooling to 0° C. over 2 hours. The precipitate thus obtained is filtered off, washed and dried under vacuum at 60° C. 2.68 kg of 1-benzyl-4-phenyl-4-piperidinecarboxamide are thus obtained;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06916929B2
出典データセットuspto-grants-2005_07
ORD IDord-caf87a1502044bfe95fd5f63f7299f11
出典メモuspto-grants-2005_07