Process for the production of 2,2,6-trimethylcyclohexane-1, 4-dione
AssigneeDegussa AG
InventorsSteffen Krill, Klaus Huthmacher, Sylvain Perrin
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Abstract
Process for the production of 2,2,6-trimethylcyclohexane-1,4-dione by epoxidation of β-isophorone with organic percarboxylic acids at a water content below 5 wt.-% and subsequent isomerization of the mixture of β-isophorone epoxide and hydroxyisophorone.
Claims20
A process for the production of dihydroketoisophorone (2,2,6-trimethylcyclohexane-1,4-dione) represented by the structure
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- comprising reacting β-isophorone (3,5,5-trimethylcyclohex-3-en-1-one) represented by the structure
- 8
- with an organic percarboxylic acid in the form of its non-aqueous solution in an inert organic solvent at a temperature of 0° C. to 300° C., the percarboxylic acid used as oxidizing agent being formed in a pre-determined equilibrium and absorbed or extracted with the solvent used for oxidation, thereby forming:
- a mixture of β-isophorone epoxide
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- and its isomer 4-hydroxyisophorone (HIP),
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- isomerizing said mixture “in situ” thermally or in the presence of an acid catalyst or in the presence of a salt.
A process for the production of an intermediate mixture of the β-isophorone epoxide represented by the structure:
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- and its isomer-4-hydroxyisophorone (HIP),
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- comprising reacting β-isophorone (3,5,5-trimethylcyclohex 3-en-1-one) represented by the structure
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- with an organic percarboxylic acid in the form of its non-aqueous solution in an inert organic solvent at a temperature of 0° C. to 300° C., the percarboxylic acid used as oxidizing agent being formed in a pre-determined equilibrium and absorbed or extracted with the solvent used for oxidation, to thereby obtain an intermediate mixture
A process for the production of dihydroketoisophorone (2,2,6-trimethylcyclohexane-1,4-dione) represented by the structure
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- comprising reacting β-isophorone (3,5,5-trimethylcyclohex-3-en-1-one) represented by the structure
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- with an organic percarboxylic acid in the form of its non-aqueous solution in an inert organic solvent at a temperature of 0° C. to 300° C., the percarboxylic acid used as oxidizing agent being formed in a pre-determined equilibrium and absorbed or extracted with the solvent used for oxidation, thereby forming:
- a mixture of β-isophorone epoxide
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- and its isomer 4-hydroxyisophorone (HIP),
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- isomerizing said mixture “in situ” thermally or in the presence of an acid catalyst or in the presence of a salt.
Dependencies are inferred from the claim text.