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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1609459생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1609459

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물N-3-BromopropylphthalimideHCID 21611—
반응물Sodium hydrideHCID 24758—
반응물1-(3-Hydroxybenzyl)piperidineHCID 826974—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-[3-(3-piperidinomethylphenoxy)propyl]phthalimideHCID 1289856586%

반응 단계

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% ).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05401739
출처 데이터셋uspto-grants-1995_03
ORD IDord-ea2612bbb173493b8c43f0d4b909199d
출처 메모uspto-grants-1995_03