4-Piperidinecarboxylic acid → 1-Acetylpiperidine-4-carboxylic acid
Reaction equation
[NH:1]1[CH2:9][CH2:8][CH:4]([C:5]([OH:7])=[O:6])[CH2:3][CH2:2]1.[C:10](OC(=O)C)(=[O:12])[CH3:11]>>[C:10]([N:1]1[CH2:9][CH2:8][CH:4]([C:5]([OH:7])=[O:6])[CH2:3][CH2:2]1)(=[O:12])[CH3:11]Participants
3
Procedure
A solution of 51.6 g of isonipecotic acid in 200 ml of acetic anhydride is refluxed for 2 hours and allowed to stir at ambient temperature for 16 hours. The solution is concentrated and the resulting residue is triturated in ether. The solid is collected by filtration and recrystallized from an isopropyl alcohol-diisopropyl ether mixture giving 1-acetylisonipecotic acid as a white solid.
Workup
- concentrationThe solution is concentrated
- customthe resulting residue is triturated in ether
- filtrationThe solid is collected by filtration
- customrecrystallized from an isopropyl alcohol-diisopropyl ether mixture
Sources & evidence
- ORD record
- ord-ce810046ab5347e79fe3fea68e6b7026
- Source dataset
- uspto-grants-1978_08
- Patent number
- US04110459
Reaction notes
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