Hydrochloric Acid → 1-Benzyl-3-(1-hydroxy-ethyl)-pyrrolidine-3-carboxylic acid methyl ester
Reaktionsgleichung
Cl.[CH3:2][O:3][C:4]([C:6]1([CH:18]([O:20]C(=O)C)[CH3:19])[CH2:10][CH2:9][N:8]([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:7]1)=[O:5]>CO>[CH3:2][O:3][C:4]([C:6]1([CH:18]([OH:20])[CH3:19])[CH2:10][CH2:9][N:8]([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:7]1)=[O:5]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2M HCl (25 ml) was added to a solution of 3-(1-Acetoxy-ethyl)-1-benzyl-pyrrolidine-3-carboxylic acid methyl ester (2N) (5 g, 16.39 mmol) in MeOH (50 ml) at room temperature, then refluxed for 2 hours. The solvent was evaporated yielding the product (4.39, 100%) ESMS (MH, 264).
Aufarbeitung
- temperaturerefluxed for 2 hours
- customThe solvent was evaporated
- customyielding the product (4.39, 100%) ESMS (MH, 264)
Quellen und Nachweise
- ORD-Eintrag
- ord-1182ddc97bed4e2b9be4b6cb55be8ced
- Quelldatensatz
- uspto-grants-2013_10
- Patentnummer
- US08546404B2
Notizen zur Reaktion
Wird geladen…