Citric Acid → HCID 66868222, compound
Reaction equation
[OH:1][N:2]1[C:7]([CH3:9])([CH3:8])[CH2:6][CH:5]([OH:10])[CH2:4][C:3]1([CH3:12])[CH3:11].[C:13]([OH:25])(=[O:24])[CH2:14][C:15]([CH2:20][C:21]([OH:23])=[O:22])([C:17]([OH:19])=[O:18])[OH:16]>O>[C:13]([O-:25])(=[O:24])[CH2:14][C:15]([CH2:20][C:21]([O-:23])=[O:22])([C:17]([OH:19])=[O:18])[OH:16].[OH:1][NH+:2]1[C:7]([CH3:8])([CH3:9])[CH2:6][CH:5]([OH:10])[CH2:4][C:3]1([CH3:12])[CH3:11].[OH:1][NH+:2]1[C:7]([CH3:8])([CH3:9])[CH2:6][CH:5]([OH:10])[CH2:4][C:3]1([CH3:12])[CH3:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a glass 0.5 L reaction bottle are added 20.0 g (116 mmol) of 1-oxyl-2,2,6,6-tetramethyl-4-hydroxypiperidine, 11.12 g (58 mmol) citric acid, 200 mg 5% Pt on C and 100 mL water. Catalytic hydrogenation is carried out at 50 psi for 30 minutes at room temperature. Catalyst is removed by filtration through a pad of Celite. The aqueous salt solution has a pH of 4.39. Removal of water yields the product as a hygroscopic glassy solid.
Workup
- customCatalyst is removed by filtration through a pad of Celite
- customRemoval of water
Sources & evidence
- ORD record
- ord-0ba2b47a740b44edaf9281e75cb574d0
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06254724B1
Reaction notes
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