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
6
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 5 grams of sodium formate and 5 grams of ammonium nitrate in 30 grams of water, and 130 grams of mineral spirits was heated at 85° C. for 7 hours while it was sparged with air at the rate of 30 liters per hour. The reaction mixture was 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% cobalt and had an acid number of 18.
Workup
- customa catalyst solution prepared
- customwas sparged with air at the rate of 30 liters per hour
- temperatureThe reaction mixture was heated at 135° C. under vacuum
- customto remove water from it
- filtrationfiltered
- additiondiluted with mineral spirits
Sources & evidence
- ORD record
- ord-e38f138075104e7b9ecf053bf7bae127
- Source dataset
- uspto-grants-1984_03
- Patent number
- US04438038
Reaction notes
Loading…