Reaktionsgleichung
[C:1]([O:7][CH2:8][CH:9]=[CH2:10])(=[O:6])[CH2:2][C:3]([CH3:5])=O.[NH:11]1[CH2:15][CH2:14][CH2:13][CH2:12]1>>[NH:11]1[CH2:15][CH2:14][CH2:13][CH:12]1[C:3]([CH3:5])=[CH:2][C:1]([O:7][CH2:8][CH:9]=[CH2:10])=[O:6]Komponenten
3
Versuchsvorschrift
Allyl 3-tetrahydropyrrolyl-2-butenoate was prepared (4.7 g, 68%) in the same manner as described in the above Example 1 (1) from allyl acetoacetate (5.0 g, 35.17 mmol) and pyrrolidine (8.8 mL, 105.51 mmol), and the obtained product was identified with the following 1H NMR data.
Quellen und Nachweise
- ORD-Eintrag
- ord-b23c8ba54c484e1bafaf208e0e2e4633
- Quelldatensatz
- uspto-grants-2006_08
- Patentnummer
- US07094908B2
Verknüpfte Notizen
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