Toluene → 1-Pyrrolidineacetic acid, ethyl ester
Reaktionsgleichung
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.Br[CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9].C1(C)C=CC=CC=1>O1CCCC1>[N:1]1([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:5][CH2:4][CH2:3][CH2:2]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To an ice bath-cooled solution of 213.4 g (3 mol) of pyrrolidine in 450 mL of tetrahydrofuran was added dropwise over about 2 hours 250.5 g (1.5 mol) of ethyl bromoacetate, maintaining the temperature below 30° C. To this solution was added 150 mL of toluene to precipitate pyrrolidinium bromide, which was separated by filtration. The filtrate was evaporated under vacuum to provide a residue of about 241 g of ethyl 1-pyrrolinidineacetate.
Aufarbeitung
- temperaturemaintaining the temperature below 30° C
- customto precipitate pyrrolidinium bromide, which
- customwas separated by filtration
- customThe filtrate was evaporated under vacuum
- customto provide a residue of about 241 g of ethyl 1-pyrrolinidineacetate
Quellen und Nachweise
- ORD-Eintrag
- ord-e8381d73f4f9423dbff70d4f1bb4f249
- Quelldatensatz
- uspto-grants-1993_09
- Patentnummer
- US05244997
Notizen zur Reaktion
Wird geladen…