Reaktionsgleichung
Cl.O.[NH:3]1[CH2:8][CH2:7][C:6](=[O:9])[CH2:5][CH2:4]1.[CH3:10][O:11][CH2:12][CH2:13]Br.C([O-])([O-])=O.[K+].[K+]>C(#N)C>[CH3:10][O:11][CH2:12][CH2:13][N:3]1[CH2:8][CH2:7][C:6](=[O:9])[CH2:5][CH2:4]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 4-piperidone monohydrate hydrochloride salt (2.2 g, 14.32 mmol, 1 eq) in acetonitrile, 2-bromoethyl methyl ether (5.9 ml, 28.6 mmol, 2 eq), and K2CO3 (2 eq) was added and heated at reflux overnight. Reaction extracted into dichloromethane (50 ml), washed with water (2×50 ml), dried (MgSO4), and evaporated in vacuo to give 1-(2-methoxy-ethyl)piperidin-4-one as a yellow oil.
Aufarbeitung
- temperatureheated
- temperatureat reflux overnight
- customReaction
- extractionextracted into dichloromethane (50 ml)
- washwashed with water (2×50 ml)
- dry with materialdried (MgSO4)
- customevaporated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-59caaf3a44d64dfa8db2a35e9a2ca071
- Quelldatensatz
- uspto-grants-2013_02
- Patentnummer
- US08383620B2
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