HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53961Erstellt: 25. Oktober 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(7-cyano-2-naphthyl)acrylate
https://huagongshe.com/reaction/53961
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | (7-Cyano-2-naphthyl)methyltriphenylphosphonium bromide | HCID 9936048 | — |
| Edukt | Ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-2-oxoacetate | HCID 10316641 | — |
| Edukt | Ethyl acetate hexane | HCID 21226206 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(7-cyano-2-naphthyl)acrylate | HCID 57005545 | 85,9% |
Reaktionsschritte
8.40 g of (7-cyano-2-naphthyl)methyltriphenylphosphoniumbromide and 5.0 g of ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-2-oxoacetate were suspended in a mixture of 100 ml of tetrahydrofuran and 100 ml of ethanol. With stirring, to the resulting suspension was added 2.51 g of 1,8-diazabicyclo[5.4.0]-7-undecene, followed by stirring for 3 hours at room temperature. After distilling off the solvent, the residue thus obtained was subjected to silica gel column chromatography using a n-hexane/ethyl acetate mixture as an elution solvent, thereby obtaining 6.06 g of ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(7-cyano-2-naphthyl)acrylate as a mixture of E and Z forms. A portion of the thus obtained compound was separated into E and Z forms.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05620991 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-fa242b898191430a8c61beb93bbd339f |
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| Quellennotiz | uspto-grants-1997_04 |
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