Reaktionsgleichung
Cl.[NH2:2][CH:3]1[CH2:8][CH2:7][CH2:6][CH:5]([C:9]([OH:11])=[O:10])[CH2:4]1.[CH3:12][CH2:13]O>>[NH2:2][CH:3]1[CH2:8][CH2:7][CH2:6][CH:5]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:4]1Komponenten
4
Versuchsvorschrift
Conc. HCl (1 mL) was added to a solution of 3-aminocyclohexanecarboxylic acid (500 mg, 3.49 mmol) in EtOH (20 mL) and stirring was continued at reflux temperature for 3 h. The reaction mixture was concentrated under reduced pressure to afford the crude, which was washed with 10% aqueous NaHCO3 solution, extracted with DCM, dried over anhydrous sodium sulphate to afford 300 mg of the title compound.
Aufarbeitung
- temperatureat reflux temperature for 3 h
- concentrationThe reaction mixture was concentrated under reduced pressure
- customto afford the crude, which
- washwas washed with 10% aqueous NaHCO3 solution
- extractionextracted with DCM
- dry with materialdried over anhydrous sodium sulphate
Quellen und Nachweise
- ORD-Eintrag
- ord-3b06fe1a972144e1ba4f97a3a703522c
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09289419B2
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