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HRID 21385作成日:2026年10月24日

Potassium Carbonate → 1-(4-chlorophenethyl)-3-(R)-(+)-(1-cyano-1,1diphenylmethyl)piperidine

https://huagongshe.com/ja/reaction/21385

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1-(2-Bromoethyl)-4-chlorobenzeneHCID 23029—
反応物3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidineHCID 22853758—
溶媒AcetonitrileHCID 6342—
生成物1-(4-chlorophenethyl)-3-(R)-(+)-(1-cyano-1,1diphenylmethyl)piperidineHCID 22853752—

反応手順

A mixture containing 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)piperidine (1 g--see Preparation 1), 4-chlorophenethyl bromide (0.72 g), anhydrous potassium carbonate (1.5 g) and acetonitrile (25 ml) was heated under reflux for 4 hours. The mixture was partitioned between dichloromethane (50 ml) and 10% aqueous potassium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (3×30 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give an oil which was purified by column chromatography on silica eluting with hexane containing dichloromethane (30% up to 70%) and then dichloromethane containing methanol (0% up to 5%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from acetonitrile to give the title compound as colourless rhombs, yield 0.85 g, m.p. 129°14 131° C. [α]D25 +20.3 (c 1.0, CH2Cl2)

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-dd99be49ecbc46eba4904d687e239f52
出典メモuspto-grants-1995_06