Reaktionsgleichung
Cl.[NH2:2][C@H:3]1[CH2:8][CH2:7][C@H:6]([C:9](O)=[O:10])[CH2:5][CH2:4]1.COCCO[AlH2-]OCCOC.[Na+].[OH-].[Na+]>O>[NH2:2][C@H:3]1[CH2:8][CH2:7][C@H:6]([CH2:9][OH:10])[CH2:5][CH2:4]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Trans-4-aminocyclohexane carboxylic acid hydrochloride (2.00 g, 14.3 mmol) was added in small portions to a stirred, hot (70-85° C.) solution of Red-Al (27.0 g) for 2 h (a semisolid formed), and heating was continued overnight. After 24 h, the reaction mixture was cooled to room temperature and treated with a solution of NaOH (3.8 g) in H2O (34 ml). Following the addition, the reaction was gradually heated to 80° C., and cooled. The toluene layer was separated and the aqueous layer was extracted with CHCl3 (3×100 ml). The organic layers were dried with MgSO4 and then concentrated under reduced pressure to provide the desired compound (1.81 g, 14.0 mmol) as a pure white solid in 50% yield. ES-MS: 130 (M+1).
Aufarbeitung
- customformed), and
- temperatureheating
- waitAfter 24 h
- additionthe addition
- temperaturethe reaction was gradually heated to 80° C.
- temperaturecooled
- customThe toluene layer was separated
- extractionthe aqueous layer was extracted with CHCl3 (3×100 ml)
- dry with materialThe organic layers were dried with MgSO4
- concentrationconcentrated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-097a7ceb6bf34ac4a3916939ff8349b5
- Quelldatensatz
- uspto-grants-2013_05
- Patentnummer
- US08440661B2
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