Hydrogen Peroxide → HCID 22117088, compound
Reaction equation
S(=O)(=O)(O)O.OO.[OH-].[Na+].[C:10]([N:23]([CH2:25][C:26]([O-:28])=[O:27])[CH3:24])(=[O:22])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21].[Na+].[Co:30]>>[C:10]([N:23]([CH2:25][C:26]([O-:28])=[O:27])[CH3:24])(=[O:22])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21].[Co+2:30].[C:10]([N:23]([CH2:25][C:26]([O-:28])=[O:27])[CH3:24])(=[O:22])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]Participants
6
Procedure
1000 ml of the cobalt solution resulting from separation of the organic phase and containing sulfuric acid, residues of hydrogen peroxide and 0.98% by weight of Co are adjusted to a pH of 6.5 by addition of about 130 g of 18% strength by weight sodium hydroxide solution and subsequently freed of hydrogen peroxide by heating to the boiling point. 333 ml of aqueous 1M sodium N-lauroylsarcosinate are subsequently added, forming cobalt N-lauroylsarcosinate in the form of a pale pink precipitate.
Workup
- temperatureby heating to the boiling point
Sources & evidence
- ORD record
- ord-98b7895e8909439fa657f5e58403cce5
- Source dataset
- uspto-grants-2000_12
- Patent number
- US06162753
Reaction notes
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