4-Phenylazetidin-2-one → 2-Phenylazetidine
Reaktionsgleichung
[C:1]1([CH:7]2[NH:10][C:9](=O)[CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[C:1]1([CH:7]2[CH2:8][CH2:9][NH:10]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
Dissolve 4-phenyl-azetidin-2-one (1.0 g, 4.28 mmol) in anhydrous THF (20 mL) and treat with 1.0 M solution of lithium aluminum hydride (8.57 mL, 2.0 equiv.) at room temperature. Stir for 15 h, cool to 0° C. in an ice bath and quench with 8.5 mL 1.0 M NaOH then 8.5 mL H2O. Filter resulting solution through celite with additional EtOAc, dry with MgSO4, filter and evaporate to yield a milky white oil that solidifies upon standing. Use 2-Phenyl-azetidine without further purification.
Aufarbeitung
- customquench with 8.5 mL 1.0 M NaOH
- filtrationFilter
- customresulting solution through celite with additional EtOAc
- dry with materialdry with MgSO4
- filtrationfilter
- customevaporate
- customto yield a milky white oil
- customUse 2-Phenyl-azetidine without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-2e1cc54868fb4c7e9658e4a58c2f0033
- Quelldatensatz
- uspto-grants-2009_09
- Patentnummer
- US07595339B2
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