3-Hydroxy-1-methylpiperidin-2-one → 1-Methylpiperidine-2,3-dione
Reaktionsgleichung
[OH:1][CH:2]1[CH2:7][CH2:6][CH2:5][N:4]([CH3:8])[C:3]1=[O:9]>CC(C)=O>[CH3:8][N:4]1[CH2:5][CH2:6][CH2:7][C:2](=[O:1])[C:3]1=[O:9]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 3-hydroxy-1-methylpiperidin-2-one (1 g, 7.59 mmol) in acetone (50 mL) was added Jones-reagent (2 mL) dropwise at room temperature. The resulting solution was stirred for 10 min at room temperature. The solid material was removed by filtration. The filtrate was concentrated in vacuo at 30-40° C. The residue was dissolved in DCM (50 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to afford the title compound (220 mg, 11%) which was used in next step immediately without further purification.
Aufarbeitung
- customThe solid material was removed by filtration
- concentrationThe filtrate was concentrated in vacuo at 30-40° C
- dissolutionThe residue was dissolved in DCM (50 mL)
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-308f8ff7226d40c1855d94c7c009a4fb
- Quelldatensatz
- uspto-grants-2014_12
- Patentnummer
- US08901313B2
Notizen zur Reaktion
Wird geladen…