HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 654093Erstellt: 24. Oktober 2026
Water → Trans-4-[4-(2-methyloxyphenyl)piperazinyl]-2-buten-1-yl-amine
https://huagongshe.com/de/reaction/654093
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 1-(2-Methoxyphenyl)-4-(4-amino-2-butynyl)piperazine | HCID 15329895 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Trans-4-[4-(2-methyloxyphenyl)piperazinyl]-2-buten-1-yl-amine | HCID 19917461 | 54,1% |
Reaktionsschritte
A solution of 1-amino-4-[4-(2-methoxyphenyl)-1-piperazinyl]-2-butyne (13.4 g) in tetrahydrofuran (150 ml) was added dropwise over 45 mins to a suspension of lithium aluminum hydride (3.91 g) in tetrahydrofuran (500 ml), while the reaction temperature was maintained below 5° C. The reaction mixture was allowed to warm to room temperature and was stirred at room temperature for 20 hrs. Water (3.9 ml), 15% aqueous sodium hydroxide (3.9 ml) and water (12 ml) were added sequentially, while the reaction temperature was kept below 30° C. The precipitate was filtered through a bed of celite, washed three times with diethyl ether (100 ml), filtered, and the filtrate was concentrated. Recrystallization of the residue from hexane gave 7.31 g (54%) of product, mp 63°-67° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05130315 |
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| Quelldatensatz | uspto-grants-1992_07 |
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| ORD ID | ord-d14d4075d623469baa56c7a9d660181f |
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| Quellennotiz | uspto-grants-1992_07 |
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