Hydrochloric Acid → Methyl 3-aminocyclohexane-1-carboxylate
Reaktionsgleichung
C(OC([NH:8][CH:9]1[CH2:14][CH2:13][CH2:12][CH:11]([C:15]([O:17][CH3:18])=[O:16])[CH2:10]1)=O)(C)(C)C.Cl.CO>O1CCOCC1>[NH2:8][CH:9]1[CH2:14][CH2:13][CH2:12][CH:11]([C:15]([O:17][CH3:18])=[O:16])[CH2:10]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In a flask, methyl 3-(tert-butoxycarbonylamino)cyclohexanecarboxylate (5.13 g, 19.94 nmol) in 1,4-dioxane (15 ml) was reacted with hydrochloric acid in dioxane (4M) (15 mL). Methanol (2 mL) was added to aid in solubility. The reaction was stirred at room temperature for 1 hour. Upon completion the reaction was concentrated, and the crude (3.86 g) was progressed to the next step without further purification.
Aufarbeitung
- concentrationUpon completion the reaction was concentrated
- customthe crude (3.86 g) was progressed to the next step without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-ba9c3c9dc6bf4702a9729a199abefd56
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09351965B2
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