戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1609459作成日:2026年10月26日

Diethyl Ether → N-[3-(3-piperidinomethylphenoxy)propyl]phthalimide

https://huagongshe.com/reaction/1609459

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物N-3-BromopropylphthalimideHCID 21611—
反応物Sodium hydrideHCID 24758—
反応物1-(3-Hydroxybenzyl)piperidineHCID 826974—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N-[3-(3-piperidinomethylphenoxy)propyl]phthalimideHCID 1289856586%

反応手順

In an argon stream, 2.2 g of 60% sodium hydride was suspended in 20 ml of N,N-dimethylformamide. The suspension was added dropwise to a solution of 9.6 g of the 3-(1-piperidinomethyl)phenol obtained in Reference Example 1 in 30 ml of N,N-dimethylformamide, followed by stirring at room temperature for 30 minutes. Next, a solution of 14.7 g of N-(3-bromopropyl)phthalimide in 50 ml of N,N-dimethylformamide was added dropwise to the mixture, and the resulting mixture was stirred at 65° C. for 8 hours. After cooling the mixture, a mixture of diethyl ether and water (1:1) was added thereto for extraction, and the organic layer was concentrated under reduced pressure. To the concentrate was added 6N hydrochloric acid for extraction into the aqueous layer, which was then made alkaline with potassium hydroxide, followed by extraction with diethyl ether. The organic layer was dried over magnesium sulfate and distilled under reduced pressure to remove the solvent, giving 16.3 g of transparent oily N-[3-[3-(piperidinomethyl)-phenoxy]propyl]phthalimide (yield 86% ).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05401739
出典データセットuspto-grants-1995_03
ORD IDord-ea2612bbb173493b8c43f0d4b909199d
出典メモuspto-grants-1995_03