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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1609459Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1609459

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktN-3-BromopropylphthalimideHCID 21611—
EduktSodium hydrideHCID 24758—
Edukt1-(3-Hydroxybenzyl)piperidineHCID 826974—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[3-(3-piperidinomethylphenoxy)propyl]phthalimideHCID 1289856586%

Reaktionsschritte

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% ).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05401739
Quelldatensatzuspto-grants-1995_03
ORD IDord-ea2612bbb173493b8c43f0d4b909199d
Quellennotizuspto-grants-1995_03