Reaktionsgleichung
C(O[C:4]1(OCC)[CH2:8][CH2:7][CH2:6][N:5]1[CH3:9])C.[Cl:13][C:14]1[CH:22]=[CH:21][C:17]([CH2:18][C:19]#[N:20])=[CH:16][CH:15]=1>C1C=CC=CC=1>[C:19]([C:18](=[C:4]1[CH2:8][CH2:7][CH2:6][N:5]1[CH3:9])[C:17]1[CH:21]=[CH:22][C:14]([Cl:13])=[CH:15][CH:16]=1)#[N:20]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Boil 22.7 g of 2,2-diethoxy-1-methylpyrrolidine, 19.8 g of 4-chlorobenzylcyanide and 90 ml of benzene for 1 hour under reflux and with stirring. Distil off the volatile constituents under a vacuum. After trituration with a little diethyl ether, filter off the residue to obtain 20.8 g (68% of theory) and the title compound (m.p. 71° to 72° from isopropanol).
Aufarbeitung
- customDistil off the volatile constituents under a vacuum
- filtrationAfter trituration with a little diethyl ether, filter off the residue
- customto obtain 20.8 g (68% of theory)
Quellen und Nachweise
- ORD-Eintrag
- ord-38d157ccb44247ad82d5a58cc7c67f0b
- Quelldatensatz
- uspto-grants-1981_07
- Patentnummer
- US04279918
Verknüpfte Notizen
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