HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1609459Erstellt: 25. Oktober 2026
Diethyl Ether → N-[3-(3-piperidinomethylphenoxy)propyl]phthalimide
https://huagongshe.com/reaction/1609459
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | N-3-Bromopropylphthalimide | HCID 21611 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 1-(3-Hydroxybenzyl)piperidine | HCID 826974 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-[3-(3-piperidinomethylphenoxy)propyl]phthalimide | HCID 12898565 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05401739 |
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| Quelldatensatz | uspto-grants-1995_03 |
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| ORD ID | ord-ea2612bbb173493b8c43f0d4b909199d |
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| Quellennotiz | uspto-grants-1995_03 |
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