戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 21393作成日:2026年10月26日

Potassium Carbonate → 3-(R, S)-(1-Cyano-1,1-diphenylmethyl)-1-(4-carbamoylphenethyl)piperidine

https://huagongshe.com/reaction/21393

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物3-(R,S)-(1-cyano-1,1-diphenylmethyl)piperidineHCID 13633746—
反応物4-Carbamoylphenethyl bromideHCID 22037884—
溶媒AcetonitrileHCID 6342—
生成物3-(R, S)-(1-Cyano-1,1-diphenylmethyl)-1-(4-carbamoylphenethyl)piperidineHCID 21224084—

反応手順

A mixture containing 3-(R,S)-(1-cyano-1,1-diphenylmethyl)piperidine (0.303 g), 4-carbamoylphenethyl bromide (0.275 g--see Preparation 5), anhydrous potassium carbonate (0.4 g) and acetonitrile (10 ml) was heated under reflux for 5 hours. The mixture was concentrated in vacuo and the residue partitioned between dichloromethane (50 ml) and 10% aqueous potassium carbonate (50 ml). The layers were separated and the aqueous layer extracted with dichloromethane (3×20 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give a gum which was purified by column chromatography on silica eluting with dichloromethane containing methanol (5%). The product-containing fractions were combined and concentrated inn vacuo to give the title compound as a gum, yield 0.065 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05422358
出典データセットuspto-grants-1995_06
ORD IDord-f3d9887db70a4013b3e8df2ebd391a4f
出典メモuspto-grants-1995_06