Sodium borohydride → (R)-4-[(1-Methyl-2,2,2-trifluoro-ethylamino)-methyl]-benzylamine
Reaktionsgleichung
[CH3:1][C@@H:2]([NH:7][CH2:8][C:9]1[CH:16]=[CH:15][C:12]([C:13]#[N:14])=[CH:11][CH:10]=1)[C:3]([F:6])([F:5])[F:4].[BH4-].[Na+]>CO.O.O.O.O.O.O.[Co](Cl)Cl>[CH3:1][C@@H:2]([NH:7][CH2:8][C:9]1[CH:10]=[CH:11][C:12]([CH2:13][NH2:14])=[CH:15][CH:16]=1)[C:3]([F:5])([F:6])[F:4]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Add cobalt(II) chloride hexahydrate (1.45 g, 6.09 mmol) to a solution of (R)-4-[(1-methyl-2,2,2-trifluoro-ethylamino)-methyl]-benzonitrile (695 mg, 3.045 mmol) in methanol (20 mL). Add sodium borohydride (1.15 g, 30.45 mmol) in small batches and stir at room temperature for 3 h. Quench with water, add chloroform and filter the mixture through Celite®. Separate layers and extract the aqueous phase twice with chloroform. Dry the combined organic extracts over MgSO4, filter and concentrate in vacuo. Purify by chromatography on silica gel (40 g) eluting with a gradient of DCM to 19:1 and 9:1 DCM/(chloroform:methanol:concentrated NH4OH 80:18:2) to obtain the title compound as an oil (0.4 g, 57%). MS (ES+) m/z: 233 (M+H)+.
Aufarbeitung
- customQuench with water
- additionadd chloroform
- filtrationfilter the mixture through Celite®
- extractionSeparate layers and extract the aqueous phase twice with chloroform
- dry with materialDry the combined organic extracts over MgSO4
- filtrationfilter
- concentrationconcentrate in vacuo
- customPurify by chromatography on silica gel (40 g)
- washeluting with a gradient of DCM to 19:1 and 9:1 DCM/(chloroform:methanol:concentrated NH4OH 80:18:2)
Quellen und Nachweise
- ORD-Eintrag
- ord-8ac68ba473c545fea86edb87522b3621
- Quelldatensatz
- uspto-grants-2014_03
- Patentnummer
- US08680091B2
Notizen zur Reaktion
Wird geladen…