Ammonium nitrate → Cobalt(2+) bis(7,7-dimethyloctanoate)
Reaction equation
[Co:1].[C:2]([OH:13])(=[O:12])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]([CH3:11])([CH3:10])[CH3:9].C([O-])=O.[Na+].[N+]([O-])([O-])=O.[NH4+]>O>[C:2]([O-:13])(=[O:12])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]([CH3:9])([CH3:10])[CH3:11].[Co+2:1].[C:2]([O-:13])(=[O:12])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]([CH3:9])([CH3:10])[CH3:11]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 85 °C
Procedure
A mixture of 50 grams of cobalt powder, 316.2 grams (1.697 moles) of neodecanoic acid (acid number, 301), a catalyst solution prepared by dissolving 2.5 grams of sodium formate and 2.5 grams of ammonium nitrate in 20 grams of water, and 130 grams of mineral spirits was heated to 85° C. and maintained at that temperature for 3.5 hours while it was sparged with air at the rate of 30 liters per hour. After the addition of a solution prepared by dissolving 2.5 grams of sodium formate and 2.5 grams of ammonium nitrate in 20 grams of water, the reaction mixture was heated at 85° C. for 2.5 hours. It was then heated at 135° C., under vacuum to remove water from it, filtered, and diluted with mineral spirits. There was obtained a solution of cobalt neodecanoate in mineral spirits that contained 10% by weight of cobalt and had an acid number of 16.
Workup
- customa catalyst solution prepared
- temperaturemaintained at that temperature for 3.5 hours while it
- customwas sparged with air at the rate of 30 liters per hour
- additionAfter the addition of a solution
- customprepared
- temperaturethe reaction mixture was heated at 85° C. for 2.5 hours
- temperatureIt was then heated at 135° C., under vacuum
- customto remove water from it
- filtrationfiltered
- additiondiluted with mineral spirits
Sources & evidence
- ORD record
- ord-bdc2c32ff47b417ba6791b834d2d5000
- Source dataset
- uspto-grants-1984_03
- Patent number
- US04438038
Reaction notes
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