4-Piperidone → 4-Oxo-N-propylpiperidine-1-carboxamide
Reaction equation
[NH:1]1[CH2:6][CH2:5][C:4](=[O:7])[CH2:3][CH2:2]1.[CH2:8]([N:11]=[C:12]=[O:13])[CH2:9][CH3:10]>>[CH2:8]([NH:11][C:12]([N:1]1[CH2:6][CH2:5][C:4](=[O:7])[CH2:3][CH2:2]1)=[O:13])[CH2:9][CH3:10]Participants
3
Procedure
To piperid-4-one (11.8 g) was added n-propyl isocyanate in small portions at room temperature with stirring. After stirring 48 hr the solvent was removed in vacuo, and the residue was treated with diethyl ether, yielding (D.31) (19.1 g, 86%) as a pale yellow oil.
Workup
- stirringAfter stirring 48 hr the solvent
- customwas removed in vacuo
- additionthe residue was treated with diethyl ether
- customyielding (D.31) (19.1 g, 86%) as a pale yellow oil
Sources & evidence
- ORD record
- ord-c1ed351b0df2415d906d4fc835725c64
- Source dataset
- uspto-grants-1986_07
- Patent number
- US04603138
Reaction notes
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