戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 972549作成日:2026年10月24日

Sodium Hydroxide → 2,2-Diphenyl-4-(4-phenylpiperidino)butyronitrile

https://huagongshe.com/ja/reaction/972549

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物4-PhenylpiperidineHCID 69873—
反応物DiisopropylethylamineHCID 81531—
反応物4-Bromo-2,2-diphenylbutyronitrileHCID 96575—
溶媒2-MethoxyethanolHCID 8019—
生成物2,2-Diphenyl-4-(4-phenylpiperidino)butyronitrileHCID 21404797—

反応手順

A mixture of 18.6 parts of 2,2-diphenyl-4-bromobutyronitrile, 10.0 parts of 4-phenylpiperidine, 8.0 parts of N,N-diisopropylethylamine and 200 parts by volume of 2-methoxyethanol is heated at reflux for 16 hours. The solution is then cooled and stripped in vacuum. The resulting residue is partitioned between dilute sodium hydroxide and ether. Extraction of the ether phase with dilute hydrochloric acid results in the precipitation of an oil. This oil and the aqueous phase of the partitioning are combined, treated with aqueous sodium hydroxide and extracted with 1:1 ether-benzene mixture. The ether-benzene extract is dried over sodium sulfate and stripped in vacuum to give a solid. Crystallization of the solid from a mixture of skelly B and ether provided 2,2-diphenyl-4-(4-phenylpiperidino)butyronitrile, melting at 88° - 89.5° C. and having the following formula ##STR7##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04053477
出典データセットuspto-grants-1977_10
ORD IDord-80f40e08ab6c4dbaa52aaa3b6f595c62
出典メモuspto-grants-1977_10