Iron → Iron(2+) bis(6-methylheptanoate)
Reaction equation
[Fe:1].[C:2]([OH:11])(=[O:10])[CH2:3][CH2:4][CH2:5][CH2:6][CH:7]([CH3:9])[CH3:8].[F-].[NH4+].C([O-])=O.[NH4+]>O>[C:2]([O-:11])(=[O:10])[CH2:3][CH2:4][CH2:5][CH2:6][CH:7]([CH3:9])[CH3:8].[Fe+2:1].[C:2]([O-:11])(=[O:10])[CH2:3][CH2:4][CH2:5][CH2:6][CH:7]([CH3:9])[CH3:8]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 95 °C
Procedure
A mixture of 46 grams (0.806 mole) of powdered iron (97.8% Fe) (100% through a 100 mesh screen), 292 grams (2.014 moles) of isooctanoic acid (acid number, 387), a catalyst solution prepared by dissolving 10 grams of ammonium fluoride and 5 grams of ammonium formate in 25 grams of water, and 170 grams of mineral spirits was sparged with air at the rate of 30 liters per hour until the exotherm had subsided. Sparging with air was continued while the reaction mixture was heated at 95° C. for 5 hours. It was then heated to 135° C. under vacuum to remove water from it, filtered, and diluted with mineral spirits. There was obtained a solution of iron isooctanoate in mineral spirits that contained 9.0% of iron.
Workup
- customa catalyst solution prepared
- customwas sparged with air at the rate of 30 liters per hour until the exotherm
- customSparging with air
- temperatureIt was then heated to 135° C. under vacuum
- customto remove water from it
- filtrationfiltered
- additiondiluted with mineral spirits
Sources & evidence
- ORD record
- ord-12c4745250e34f4e80c5a209f3a592b8
- Source dataset
- uspto-grants-1982_06
- Patent number
- US04337208
Reaction notes
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