戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 992363作成日:2026年10月23日

Methanol → 4-(4-Phenoxyphenyl)piperidine

https://huagongshe.com/ja/reaction/992363

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物4-(4-Phenoxyphenyl)-1,2,3,6-tetrahydropyridineHCID 22599989—
触媒HCID 178418390HCID 178418390—
溶媒Acetic AcidHCID 176—
生成物4-(4-Phenoxyphenyl)piperidineHCID 1107598466%

反応手順

To a 100 ml methanol solution of 3.51 g of the compound (8) synthesized in Example 1 were added 200 mg of palladium carbon and 1 ml of acetic acid for hydrogenation at atmospheric pressure and room temperature. After the completion of the reaction, the insolubles were filtered off, then the filtrate was concentrated under reduced pressure. The obtained residue was dissolved in methylene chloride and adjusted by a 10% aqueous solution of sodium hydroxide to a pH 9 to 10, then was shaken. The organic layer was dried, filtered, then condensed under reduced pressure to obtain a residue which was then purified by silica gel column chromatography (methylene chloride:methanol=20:1) to obtain the above-referenced compound (9) in an amount of 2.32 g (yield 66%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06469010B1
出典データセットuspto-grants-2002_10
ORD IDord-68b176c97cf44b6fa785f4d2168d0504
出典メモuspto-grants-2002_10