Trifluoroacetic acid → HCID 86738262, compound
Reaction equation
C([CH:3]([CH2:7][CH2:8][CH2:9][CH3:10])[C:4]([OH:6])=[O:5])C.[F:11][C:12]([F:17])([F:16])[C:13]([OH:15])=[O:14].[OH-].[Na+].O.O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Ni+2:32]>CO>[F:11][C:12]([F:17])([F:16])[C:13]([O-:15])=[O:14].[C:4]([O:6][CH2:12][CH3:13])(=[O:5])[CH2:3][CH2:7][CH2:8][CH2:9][CH3:10].[Ni+2:32].[F:11][C:12]([F:17])([F:16])[C:13]([O-:15])=[O:14]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
14.4 g of 2-ethyl hexanoic acid (0.1 mole), 100 cm3 of methanol, 11.4 g of trifluoroacetic acid (0.1 mole) and 8.0 g of sodium hydroxide (0.2 mole) are successively fed into a 500 cm3 glass reaction vessel provided with a magnetic stirring rod and a reflux device. The mixture is heated to reflux and 35.1 g (0.125 mole) of nickel sulfate heptahydrate is added. The mixture is heated again at reflux. Methanol is evaporated by means of a rotative evaporator and the residue is taken up in toluene. After filtration of the insoluble inorganic salts, toluene is distilled off and nickel 2-ethyl hexanoate trifluoroacetate is obtained. Its analysis corresponds to the formula C10H15O4F3Ni and it has the same characteristic bands as the product of example 1.
Workup
- customprovided with a magnetic stirring rod
- temperatureThe mixture is heated
- temperatureto reflux
- temperatureThe mixture is heated again
- temperatureat reflux
- customMethanol is evaporated by means of a rotative evaporator
- filtrationAfter filtration of the insoluble inorganic salts, toluene
- distillationis distilled off
Sources & evidence
- ORD record
- ord-6c7510a191144e44b7785b2a5b351c9d
- Source dataset
- uspto-grants-1983_08
- Patent number
- US04398049
Reaction notes
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