Hydrochloric Acid → 4-Diisopropylaminobutyric acid hydrochloride
Reaktionsgleichung
[ClH:1].CN1CCCC(C(O)=O)C1.[CH:12]([N:15]([CH:24]([CH3:26])[CH3:25])[CH2:16][CH2:17][CH2:18][C:19]([O:21]CC)=[O:20])([CH3:14])[CH3:13].Cl>>[ClH:1].[CH:24]([N:15]([CH:12]([CH3:14])[CH3:13])[CH2:16][CH2:17][CH2:18][C:19]([OH:21])=[O:20])([CH3:26])[CH3:25]Komponenten
4
Versuchsvorschrift
4-Diisopropylaminobutyric acid hydrochloride may be obtained by working according to the method described in Example 4 for the preparation of 1-methyl-3-piperidinecarboxylic acid hydrochloride, but starting with ethyl 4-diisopropylaminobutyrate (9.2 g) and 6 N aqueous hydrochloric acid solution (28.5 cc) and by heating for 6 hours under reflux. 4-Diisopropylaminobutyric acid hydrochloride (8 g), m.p. 136° C., is thereby obtained.
Aufarbeitung
- temperatureby heating for 6 hours
- temperatureunder reflux
Quellen und Nachweise
- ORD-Eintrag
- ord-b915410b6fbb47b2a8b507389b39408f
- Quelldatensatz
- uspto-grants-1992_04
- Patentnummer
- US05102890
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