戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2285916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/2285916

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—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物Piperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl-HCID 306039250.3%

反応手順

A solution of 1-methyl-4-(4-nitrophenoxy)-4-phenylpiperidine (4.4 g, 14.1 mM) in methanol (250 ml) was hydrogenated at 1 atmosphere and ambient temperature over 5% palladium on charcoal (500 mg) until the theoretical uptake of hydrogen had occurred (about 2 hours). The catalyst was removed by filtration and the solvent evaporated under reduced pressure. Recrystallisation of the residue from IPA gave the title compound (2 g) m.p. 174°-5°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04325953
出典データセットuspto-grants-1982_04
ORD IDord-087ae6c0a6d144b4b3419ed8322470da
出典メモuspto-grants-1982_04