Ammonium nitrate → Cobalt(2+) bis(7,7-dimethyloctanoate)

HRID 1903695Notes

Reaction equation

HRID 1903695 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

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

  1. customa catalyst solution prepared
  2. temperaturemaintained at that temperature for 3.5 hours while it
  3. customwas sparged with air at the rate of 30 liters per hour
  4. additionAfter the addition of a solution
  5. customprepared
  6. temperaturethe reaction mixture was heated at 85° C. for 2.5 hours
  7. temperatureIt was then heated at 135° C., under vacuum
  8. customto remove water from it
  9. filtrationfiltered
  10. 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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