Cyclohexanone → 1-Cyclohexylpyrrolidine
Reaktionsgleichung
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[C:6]1(=O)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.[O-]S([O-])(=O)=O.[Mg+2]>C1CCCCC1>[CH:6]1([N:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Cyclohexylpyrrolidine was prepared as described in the procedure below illustrated in Scheme 1. In a 3-neck reaction flask equipped with a mechanical stirrer and heating mantle, a 2 molar equivalent of pyrrolidine were mixed with 1 molar equivalent of cyclohexanone in dry cyclohexane to make a 1M solution with respect to the cyclohexanone. To the mixture, 2 molar equivalents of anhydrous MgSO4 (as dehydrating agent) were added. The resulting mixture was refluxed for 94 hours. The progress of the reaction was monitored by NMR analysis.
Aufarbeitung
- customIn a 3-neck reaction flask equipped with a mechanical stirrer
- temperatureheating mantle
- temperatureThe resulting mixture was refluxed for 94 hours
Quellen und Nachweise
- ORD-Eintrag
- ord-b7724158c78141338e8d3ee33dce76d4
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09108856B2
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