Process for isomerization and decarboxylation of unsaturated organic compounds with a metal catalyst or catalyst precursor
US-9868679-B2 · Jan 16, 2018 · US
US11186802B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11186802-B2 |
| Application number | US-202016918187-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 1, 2020 |
| Priority date | Jul 29, 2019 |
| Publication date | Nov 30, 2021 |
| Grant date | Nov 30, 2021 |
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Disclosed herein are processes for the decarboxylation, isomerization, hydrogenation, dehydrogenation, and cyclization/aromatization of fatty acids involving contacting a starting material which is an unsaturated fatty acid, unsaturated fatty acid derivative, or an unsaturated triglyceride, in the presence of a catalyst at a temperature at which decarboxylation, isomerization, hydrogenation, dehydrogenation, and cyclization/aromatization occurs and recovering the unsaturated organic compound product; wherein the catalyst is chloro-1,5-cyclooctadiene iridium (I) dimer. The product may contain at least about 8% by volume aromatic content and less than about 25% by volume aromatic content, and wherein the product contains less than about 1% by volume of naphthalenes.
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We claim: 1. A process for the decarboxylation, isomerization, hydrogenation, dehydrogenation, and cyclization/aromatization of fatty acids, said process comprising contacting a starting material which is an unsaturated fatty acid, unsaturated fatty acid derivative, or an unsaturated triglyceride, in the presence of a catalyst at a temperature at which decarboxylation, isomerization, hydrogenation, dehydrogenation, and cyclization/aromatization occurs and recovering the unsaturated organic compound product; wherein said catalyst is chloro-1,5-cyclooctadiene iridium (I) dimer. 2. The process according to claim 1 , wherein said product contains at least about 8% by volume aromatic content and less than about 25% by volume aromatic content, and wherein said product contains less than about 1% by volume of naphthalenes. 3. The process according to claim 1 , wherein said product contains at least about 8% by volume aromatic content and less than about 25% by volume aromatic content, and wherein said product contains less than about 0.1% by volume of naphthalenes. 4. The process according to claim 1 , wherein said starting material is a mixture of fatty acids. 5. The process according to claim 1 , wherein said starting material is soybean oil based fatty acids. 6. The process according to claim 1 , wherein said starting material is at least about 80% oleic soybean oil based fatty acids. 7. The process according to claim 1 , wherein said catalyst is chloro-1,5-cyclooctadiene iridium (I) dimer and at least one Ru catalyst.
by isomerisation {(isomerisation induced by hydrogenation C11C3/12)} · CPC title
Iridium · CPC title
Bi- or polynuclear complexes, i.e. comprising two or more metal coordination centres, without metal-metal bonds, e.g. Cp(Lx)Zr-imidazole-Zr(Lx)Cp · CPC title
Ruthenium · CPC title
using catalysts based principally on other metals or derivates · CPC title
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