ES2657652T3 - Procedimiento para la preparación de ácidos ciclohexanodicarboxílicos y sus derivados - Google Patents
Procedimiento para la preparación de ácidos ciclohexanodicarboxílicos y sus derivados Download PDFInfo
- Publication number
- ES2657652T3 ES2657652T3 ES02701282.2T ES02701282T ES2657652T3 ES 2657652 T3 ES2657652 T3 ES 2657652T3 ES 02701282 T ES02701282 T ES 02701282T ES 2657652 T3 ES2657652 T3 ES 2657652T3
- Authority
- ES
- Spain
- Prior art keywords
- acid anhydride
- mixture
- butadiene
- conversion
- cyclohexanedicarboxylic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims abstract description 56
- 230000008569 process Effects 0.000 title claims abstract description 47
- 238000002360 preparation method Methods 0.000 title claims abstract description 32
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical class OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 title claims abstract description 30
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims abstract description 134
- 239000000203 mixture Substances 0.000 claims abstract description 128
- 238000006243 chemical reaction Methods 0.000 claims abstract description 70
- 150000002148 esters Chemical class 0.000 claims abstract description 36
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims abstract description 34
- LNPQMDSMIGLHSR-UHFFFAOYSA-N 2-oxaspiro[3.5]non-5-ene-1,3-dione Chemical compound O=C1OC(=O)C11C=CCCC1 LNPQMDSMIGLHSR-UHFFFAOYSA-N 0.000 claims abstract description 29
- FFPOAADRIDYUKW-UHFFFAOYSA-N buta-1,3-diene;furan-2,5-dione Chemical compound C=CC=C.O=C1OC(=O)C=C1 FFPOAADRIDYUKW-UHFFFAOYSA-N 0.000 claims abstract description 28
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 27
- 230000003647 oxidation Effects 0.000 claims abstract description 27
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 27
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 21
- 150000005690 diesters Chemical class 0.000 claims abstract description 21
- HHCHLHOEAKKCAB-UHFFFAOYSA-N 2-oxaspiro[3.5]nonane-1,3-dione Chemical compound O=C1OC(=O)C11CCCCC1 HHCHLHOEAKKCAB-UHFFFAOYSA-N 0.000 claims abstract description 19
- 150000001934 cyclohexanes Chemical class 0.000 claims abstract description 10
- 125000000596 cyclohexenyl group Chemical class C1(=CCCCC1)* 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 39
- 150000001993 dienes Chemical class 0.000 claims description 30
- -1 cyclohexanedicarboxylic acid ester esters Chemical class 0.000 claims description 24
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 23
- 239000004014 plasticizer Substances 0.000 claims description 22
- 229920003023 plastic Polymers 0.000 claims description 20
- 239000004033 plastic Substances 0.000 claims description 20
- 239000002253 acid Substances 0.000 claims description 9
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 9
- 239000004800 polyvinyl chloride Substances 0.000 claims description 8
- WXYTXCXWNITTLN-UHFFFAOYSA-N 3-methylcyclohexane-1,2-dicarboxylic acid Chemical compound CC1CCCC(C(O)=O)C1C(O)=O WXYTXCXWNITTLN-UHFFFAOYSA-N 0.000 claims description 7
- YWVFNWVZBAWOOY-UHFFFAOYSA-N 4-methylcyclohexane-1,2-dicarboxylic acid Chemical compound CC1CCC(C(O)=O)C(C(O)=O)C1 YWVFNWVZBAWOOY-UHFFFAOYSA-N 0.000 claims description 6
- 238000005336 cracking Methods 0.000 claims description 6
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 6
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims description 4
- 150000001735 carboxylic acids Chemical class 0.000 claims description 2
- 150000008065 acid anhydrides Chemical class 0.000 abstract description 2
- 239000003054 catalyst Substances 0.000 description 30
- 229930195733 hydrocarbon Natural products 0.000 description 21
- 150000002430 hydrocarbons Chemical class 0.000 description 21
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 12
- 239000012071 phase Substances 0.000 description 12
- 239000000047 product Substances 0.000 description 10
- 239000004805 Cyclohexane-1,2-dicarboxylic acid Substances 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 7
- 238000005698 Diels-Alder reaction Methods 0.000 description 7
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 7
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 7
- 150000001298 alcohols Chemical class 0.000 description 7
- 239000012045 crude solution Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 150000008064 anhydrides Chemical class 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 6
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 6
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 5
- QDTDKYHPHANITQ-UHFFFAOYSA-N 7-methyloctan-1-ol Chemical compound CC(C)CCCCCCO QDTDKYHPHANITQ-UHFFFAOYSA-N 0.000 description 5
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 5
- 230000032050 esterification Effects 0.000 description 5
- 238000005886 esterification reaction Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 5
- 125000005498 phthalate group Chemical class 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 4
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- 238000007670 refining Methods 0.000 description 4
- OEMSKMUAMXLNKL-UHFFFAOYSA-N 5-methyl-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C(C)=CCC2C(=O)OC(=O)C12 OEMSKMUAMXLNKL-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000001273 butane Substances 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecanol group Chemical group C(CCCCCCCCCCC)O LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 3
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical class CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000012442 inert solvent Substances 0.000 description 3
- 235000013847 iso-butane Nutrition 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pentene-2 Natural products CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 3
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 2
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 2
- XPEKVUUBSDFMDR-UHFFFAOYSA-N 4-methyl-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound CC1C=CCC2C(=O)OC(=O)C12 XPEKVUUBSDFMDR-UHFFFAOYSA-N 0.000 description 2
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 2
- 238000006261 Adler reaction Methods 0.000 description 2
- 241000132092 Aster Species 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920001944 Plastisol Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical class OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000006471 dimerization reaction Methods 0.000 description 2
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 210000002824 peroxisome Anatomy 0.000 description 2
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- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000035755 proliferation Effects 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- YLQLIQIAXYRMDL-UHFFFAOYSA-N propylheptyl alcohol Chemical compound CCCCCC(CO)CCC YLQLIQIAXYRMDL-UHFFFAOYSA-N 0.000 description 2
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- 239000000126 substance Substances 0.000 description 2
- QSAWQNUELGIYBC-OLQVQODUSA-N (1s,2r)-cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)[C@H]1CCCC[C@H]1C(O)=O QSAWQNUELGIYBC-OLQVQODUSA-N 0.000 description 1
- NMRPBPVERJPACX-UHFFFAOYSA-N (3S)-octan-3-ol Natural products CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 1
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- IIOYAXLMGNWCQN-UHFFFAOYSA-N 1-methylcyclohex-4-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1(C)CC=CCC1C(O)=O IIOYAXLMGNWCQN-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- MUZDXNQOSGWMJJ-UHFFFAOYSA-N 2-methylprop-2-enoic acid;prop-2-enoic acid Chemical class OC(=O)C=C.CC(=C)C(O)=O MUZDXNQOSGWMJJ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
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- 241001465754 Metazoa Species 0.000 description 1
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- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical class [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
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- 238000004806 packaging method and process Methods 0.000 description 1
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- 235000012239 silicon dioxide Nutrition 0.000 description 1
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- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-N sodium;hydron;carbonate Chemical compound [Na+].OC(O)=O UIIMBOGNXHQVGW-UHFFFAOYSA-N 0.000 description 1
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- 238000003786 synthesis reaction Methods 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/54—Preparation of carboxylic acid anhydrides
- C07C51/567—Preparation of carboxylic acid anhydrides by reactions not involving carboxylic acid anhydride groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/12—Esters; Ether-esters of cyclic polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10107366 | 2001-02-16 | ||
| DE10107366 | 2001-02-16 | ||
| DE10131260 | 2001-06-29 | ||
| DE2001131260 DE10131260A1 (de) | 2001-06-29 | 2001-06-29 | Verfahren zur Herstellung von Cyclohexandicarbonsäuren deren Derivaten |
| DE10161010 | 2001-12-12 | ||
| DE2001161010 DE10161010A1 (de) | 2001-12-12 | 2001-12-12 | Verfahren zur Herstellung von Cyclohexandicarbonsäuren und deren Derivaten |
| PCT/EP2002/001661 WO2002066412A1 (de) | 2001-02-16 | 2002-02-15 | Verfahren zur herstellung von cyclohexandicarbonsäuren und deren derivaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2657652T3 true ES2657652T3 (es) | 2018-03-06 |
Family
ID=27214298
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES02701282.2T Expired - Lifetime ES2657652T3 (es) | 2001-02-16 | 2002-02-15 | Procedimiento para la preparación de ácidos ciclohexanodicarboxílicos y sus derivados |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7319161B2 (enExample) |
| EP (1) | EP1363868B1 (enExample) |
| JP (1) | JP4898079B2 (enExample) |
| KR (1) | KR100634254B1 (enExample) |
| CN (3) | CN101024704B (enExample) |
| AU (1) | AU2002234635A1 (enExample) |
| ES (1) | ES2657652T3 (enExample) |
| PL (1) | PL207365B1 (enExample) |
| WO (1) | WO2002066412A1 (enExample) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0227087D0 (en) * | 2002-11-20 | 2002-12-24 | Exxonmobil Chem Patents Inc | Hydrogenation of benzene polycarboxylic acids or derivatives thereof |
| DE102004063673A1 (de) * | 2004-12-31 | 2006-07-13 | Oxeno Olefinchemie Gmbh | Verfahren zur kontinuierlichen katalytischen Hydrierung von hydrierbaren Verbindungen an festen, im Festbett angeordneten Katalysatoren mit einem wasserstoffhaltigen Gas |
| US20090149584A1 (en) * | 2006-04-21 | 2009-06-11 | Klemens Massonne | Use of hexahydrophthalimide combinations as softener |
| CN1962736B (zh) * | 2006-11-16 | 2010-10-06 | 南亚塑胶工业股份有限公司 | 一种环己烷-1,2-二羧酸异壬酯增塑剂的制造方法 |
| US20100028528A1 (en) * | 2006-12-19 | 2010-02-04 | Basf Se | Use of cyclohexane polycarbonic acid esters for the production of coating materials for the coil coating method and the production of coated coils |
| CN101990560A (zh) * | 2007-12-21 | 2011-03-23 | 埃克森美孚化学专利公司 | 助增塑剂体系 |
| DE102008001655A1 (de) * | 2008-05-08 | 2009-11-12 | Kuraray Europe Gmbh | Weichmacherhaltige Folien aus Polyvinylacetal mit Cyclohexan-1,2-dicarbon-säureestern als Weichmacher |
| US20100113664A1 (en) * | 2008-06-11 | 2010-05-06 | Ferro Corporation | Asymmetric Cyclic Diester Compounds |
| CN101343381B (zh) * | 2008-08-27 | 2011-12-21 | 南亚塑胶工业股份有限公司 | 一种六氢邻苯二甲酸酯化合物及其制备方法 |
| WO2010148081A2 (en) | 2009-06-16 | 2010-12-23 | Draths Corporation | Novel terephthalic and trimellitic based acids and carboxylate derivatives thereof |
| US8367859B2 (en) | 2009-06-16 | 2013-02-05 | Amyris, Inc. | Cyclohexane 1,4 carboxylates |
| WO2010148070A2 (en) | 2009-06-16 | 2010-12-23 | Draths Corporation | Biobased polyesters |
| US8426639B2 (en) * | 2009-06-16 | 2013-04-23 | Amyris, Inc. | Preparation of trans, trans muconic acid and trans, trans muconates |
| CN101696200B (zh) * | 2009-10-30 | 2011-09-07 | 濮阳惠成化工有限公司 | 内亚甲基六氢邻苯二甲酸酐及其生产方法 |
| MX2012007944A (es) | 2010-01-08 | 2012-08-15 | Amyris Inc | Metodos para producir isomeros de acido muconico y sales de muconato. |
| CN101863768B (zh) * | 2010-05-14 | 2013-06-05 | 中国林业科学研究院林产化学工业研究所 | 半干性油或干性油全质利用制备增塑剂及润滑剂的方法 |
| DE102010061867A1 (de) | 2010-11-24 | 2012-05-24 | Evonik Oxeno Gmbh | Verwendung von Di(isononyl)cyclohexansäureester (DINCH) in verschäumbaren PVC-Formulierungen |
| EP2655511B1 (de) | 2010-12-23 | 2016-04-06 | INEOS Styrolution Europe GmbH | Thermoplastische elastomer-zusammensetzung und verfahren zu deren herstellung |
| WO2012158250A1 (en) | 2011-05-13 | 2012-11-22 | Amyris, Inc. | Plasticizers |
| US20130171385A1 (en) * | 2011-12-29 | 2013-07-04 | Exxonmobil Research And Engineering Company | Reacting cyclopentadiene and maleic anhydride for the production of plasticizers |
| ITMI20120634A1 (it) | 2012-04-17 | 2013-10-18 | Bio On S R L | Composizione comprendente almeno un polimero biodegradabile e almeno un plastificante |
| WO2016099062A1 (ko) * | 2014-12-18 | 2016-06-23 | 한화케미칼 주식회사 | 스트리핑 방법 |
| KR101833982B1 (ko) | 2014-12-18 | 2018-04-13 | 한화케미칼 주식회사 | 스트리핑 방법 |
| EP3405518B1 (de) | 2016-01-20 | 2019-11-06 | Basf Se | Weichmacher-zusammensetzung, die aliphatische dicarbonsäureester und diester, die unter 1,2-cyclohexandicarbonsäureestern und terephthalsäureestern ausgewählt sind, enthält |
| KR102090294B1 (ko) * | 2016-04-22 | 2020-03-17 | 주식회사 엘지화학 | 가소제 조성물 및 이를 포함하는 수지 조성물 |
| JP7242635B2 (ja) * | 2018-03-27 | 2023-03-20 | 出光興産株式会社 | 潤滑油基油、該潤滑油基油を含有する潤滑油組成物、及び該潤滑油組成物を用いた無段変速機 |
| RU2691739C1 (ru) * | 2018-05-08 | 2019-06-18 | Сергей Николаевич Лакеев | Способ получения нефталатного смесевого пластификатора |
| KR102122003B1 (ko) * | 2018-11-26 | 2020-06-11 | 상명대학교산학협력단 | 스크린 타입의 노보난 유도체 화합물, 이의 제조 방법 및 이의 용도 |
| RU2754913C1 (ru) * | 2020-12-08 | 2021-09-08 | Общество с ограниченной ответственностью "Экологичная нефтехимия" | Способ селективного получения экзо,экзо- и эндо,эндо-ди(2-этилгексил)норборнен-2,3-дикарбоксилатов из с5 фракции жидких продуктов пиролиза |
| CN112851920B (zh) * | 2020-12-31 | 2021-12-07 | 东胜化学(上海)有限公司 | 一种醇酸树脂及其制备方法 |
| WO2024256670A1 (de) | 2023-06-15 | 2024-12-19 | Basf Se | Weichmacher-zusammensetzung |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2794811A (en) * | 1954-06-03 | 1957-06-04 | Allied Chem & Dye Corp | Production of cis-cyclohexane-1, 2-dicarboxylic anhydride |
| US3308086A (en) * | 1963-08-30 | 1967-03-07 | Union Carbide Corp | Ethylene copolymers with vinyl esters plasticized with phosphate and carboxylic esters |
| DE2823165A1 (de) * | 1978-05-26 | 1979-11-29 | Bayer Ag | Verfahren zur herstellung von cycloaliphatischen carbonsaeureestern |
| JP3142651B2 (ja) | 1992-07-14 | 2001-03-07 | 東燃ゼネラル石油株式会社 | 飽和脂環式ジカルボン酸無水物の製造法 |
| JP3106411B2 (ja) * | 1992-12-21 | 2000-11-06 | 東和化成工業株式会社 | １，４−シクロヘキサンジカルボン酸の製造方法 |
| US5399742A (en) * | 1993-06-15 | 1995-03-21 | Eastman Chemical Company | Low pressure process for the manufacture of cyclohexanedicarboxylate esters |
| JPH10212285A (ja) | 1997-01-30 | 1998-08-11 | Yuka Shell Epoxy Kk | 無水カルボン酸の製造方法 |
| CA2315223C (en) * | 1997-12-19 | 2010-02-09 | Basf Aktiengesellschaft | Method for hydrogenating benzene polycarboxylic acids or derivatives thereof by using a catalyst containing macropores |
| DE19927978A1 (de) | 1999-06-18 | 2000-12-21 | Basf Ag | Ausgewählte Cyclohexan-1,3- und 1,4-dicarbonsäureester |
| DE19927977A1 (de) * | 1999-06-18 | 2000-12-21 | Basf Ag | Verwendung von Cyclohexanpolycarbonsäuren als Weichmacher zur Herstellung toxikologisch günstig zu bewertender Kunststoffe |
-
2002
- 2002-02-15 CN CN2007100913715A patent/CN101024704B/zh not_active Expired - Fee Related
- 2002-02-15 WO PCT/EP2002/001661 patent/WO2002066412A1/de not_active Ceased
- 2002-02-15 CN CN200710091372XA patent/CN101024705B/zh not_active Expired - Fee Related
- 2002-02-15 ES ES02701282.2T patent/ES2657652T3/es not_active Expired - Lifetime
- 2002-02-15 KR KR1020037010716A patent/KR100634254B1/ko not_active Expired - Fee Related
- 2002-02-15 EP EP02701282.2A patent/EP1363868B1/de not_active Expired - Lifetime
- 2002-02-15 JP JP2002565930A patent/JP4898079B2/ja not_active Expired - Fee Related
- 2002-02-15 PL PL371671A patent/PL207365B1/pl unknown
- 2002-02-15 AU AU2002234635A patent/AU2002234635A1/en not_active Abandoned
- 2002-02-15 US US10/467,234 patent/US7319161B2/en not_active Expired - Fee Related
- 2002-02-15 CN CNB028050991A patent/CN1318372C/zh not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN101024704B (zh) | 2010-08-18 |
| KR20030078919A (ko) | 2003-10-08 |
| CN101024705B (zh) | 2012-06-20 |
| KR100634254B1 (ko) | 2006-10-16 |
| CN1318372C (zh) | 2007-05-30 |
| JP4898079B2 (ja) | 2012-03-14 |
| US20040054220A1 (en) | 2004-03-18 |
| PL371671A1 (en) | 2005-06-27 |
| EP1363868B1 (de) | 2017-11-01 |
| WO2002066412A1 (de) | 2002-08-29 |
| JP2004538252A (ja) | 2004-12-24 |
| CN1501905A (zh) | 2004-06-02 |
| CN101024704A (zh) | 2007-08-29 |
| PL207365B1 (pl) | 2010-12-31 |
| AU2002234635A1 (en) | 2002-09-04 |
| EP1363868A1 (de) | 2003-11-26 |
| US7319161B2 (en) | 2008-01-15 |
| CN101024705A (zh) | 2007-08-29 |
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