Sodium borohydride → HCID 70028630, Verbindung
Reaktionsgleichung
[BH4-].[Na+].[CH2:3]([N:10]1[CH2:15][CH2:14][C:13](=[O:16])[CH:12]([CH2:17][CH2:18][CH2:19][CH3:20])[CH2:11]1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>CO>[CH2:3]([N:10]1[CH2:15][CH2:14][CH:13]([OH:16])[CH:12]([CH2:17][CH2:18][CH2:19][CH3:20])[CH2:11]1)[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Sodium borohydride (0.4 g, 12.2 mmole) was added to the stirred solution of 1-benzyl-3-n-butylpiperidin-4-one (2.8 g, 9.3 mmole) in methanol (20 ml) at 0-5° C. over a period of 5 min, and stirring was continued for 1 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water (20 ml) and extracted with ethyl acetate. The ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to furnish 1-benzyl-3-n-butyl-4-hydroxypiperidine as oil. Yield 2.5 g (86%), C16H25NO, m/z 248 (M+1).
Aufarbeitung
- concentrationThe reaction mixture was concentrated to dryness
- customtriturated with water (20 ml)
- extractionextracted with ethyl acetate
- extractionThe ethyl acetate extract
- dry with materialwas dried (Na2SO4)
- concentrationconcentrated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-a64e2511cd1e436288b5d999e27e4f69
- Quelldatensatz
- uspto-grants-2003_08
- Patentnummer
- US06608078B2
Notizen zur Reaktion
Wird geladen…