Hydrogen Bromide → 3-[(2-Aminoethyl)thiomethyl]isoxazole hydrobromide
Reaktionsgleichung
Cl[CH2:2][C:3]1[CH:7]=[CH:6][O:5][N:4]=1.Cl.[NH2:9][CH2:10][CH2:11][SH:12].[BrH:13]>>[BrH:13].[NH2:9][CH2:10][CH2:11][S:12][CH2:2][C:3]1[CH:7]=[CH:6][O:5][N:4]=1Komponenten
4
Versuchsvorschrift
A solution of 3-chloromethylisoxazole (5.8 g) and cysteamine hydrochloride (6.25 g) in aqueous hydrobromic acid (48%, 100 ml) was heated under reflux for 6 hours. Concentration in the presence of water and subsequently n-propanol, followed by recrystallisation of the residue from isopropyl alcohol-ethanol afforded 3-[(2-aminoethyl)thiomethyl]isoxazole hydrobromide, m.p. 131°-133°.
Aufarbeitung
- temperatureunder reflux for 6 hours
- concentrationConcentration in the presence of water and subsequently n-propanol
- customfollowed by recrystallisation of the residue from isopropyl alcohol-ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-59b3b79129dc45839cbb62ddbe09b620
- Quelldatensatz
- uspto-grants-1979_05
- Patentnummer
- US04153704
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