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HRID 1156028作成日:2026年10月27日

Piperidine, 1-methyl-4-(4-nitrophenoxy)-4-phenyl- → Piperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl-

https://huagongshe.com/reaction/1156028

反応式

関与物質

役割名称HCID仕込み量
反応物Piperidine, 1-methyl-4-(4-nitrophenoxy)-4-phenyl-HCID 3060390—
触媒PlatinumHCID 23939—
溶媒EthanolHCID 702—
生成物Piperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl-HCID 306039274.4%

反応手順

51 g of 1-methyl-4-(4-nitrophenoxy)-4-phenylpiperidine are dissolved in 1.5 liters of ethanol and are hydrogenated under a hydrogen pressure of 1 atmosphere in the presence of platinum. The catalyst is filtered off, the filtrate is concentrated to 300 ml and crystals (which have separated out) are collected. 34.3 g of the title compound of m.p. 173° to 174° C. are obtained by successive concentration of the filtrate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04333942
出典データセットuspto-grants-1982_06
ORD IDord-8ad115a3f6d441419d4866e6503e5fc5
出典メモuspto-grants-1982_06