JP4333471B2 - ジカルボン酸ジエステルの製造方法 - Google Patents
ジカルボン酸ジエステルの製造方法 Download PDFInfo
- Publication number
- JP4333471B2 JP4333471B2 JP2004141152A JP2004141152A JP4333471B2 JP 4333471 B2 JP4333471 B2 JP 4333471B2 JP 2004141152 A JP2004141152 A JP 2004141152A JP 2004141152 A JP2004141152 A JP 2004141152A JP 4333471 B2 JP4333471 B2 JP 4333471B2
- Authority
- JP
- Japan
- Prior art keywords
- tetrahydrophthalate
- hexahydrophthalate
- phthalate
- alcohol
- isobutyl
- 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
- -1 dicarboxylic acid diester Chemical class 0.000 title claims description 183
- 238000004519 manufacturing process Methods 0.000 title claims description 31
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 117
- 239000002994 raw material Substances 0.000 claims description 37
- 238000011084 recovery Methods 0.000 claims description 37
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 28
- 239000002253 acid Substances 0.000 claims description 18
- 238000005886 esterification reaction Methods 0.000 claims description 16
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 claims description 14
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 13
- 238000001704 evaporation Methods 0.000 claims description 10
- 230000008020 evaporation Effects 0.000 claims description 10
- QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 claims description 9
- 150000002978 peroxides Chemical class 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 6
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 claims description 5
- 230000032050 esterification Effects 0.000 claims description 5
- GEWZPNMYMLQKGF-UHFFFAOYSA-N 2-o-(2-ethylhexyl) 1-o-(2-methylpropyl) benzene-1,2-dicarboxylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C GEWZPNMYMLQKGF-UHFFFAOYSA-N 0.000 claims description 4
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 claims description 4
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 claims description 4
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 4
- DIMOQAGSNHTROK-UHFFFAOYSA-N bis(2-ethylhexyl) cyclohexane-1,2-dicarboxylate Chemical compound CCCCC(CC)COC(=O)C1CCCCC1C(=O)OCC(CC)CCCC DIMOQAGSNHTROK-UHFFFAOYSA-N 0.000 claims description 4
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims description 4
- JMXKSZRRTHPKDL-UHFFFAOYSA-N titanium ethoxide Chemical compound [Ti+4].CC[O-].CC[O-].CC[O-].CC[O-] JMXKSZRRTHPKDL-UHFFFAOYSA-N 0.000 claims description 4
- HSRUUIXSSLZEHN-UHFFFAOYSA-N 1-O-(2-ethylhexyl) 2-O-(2-methylpropyl) cyclohex-3-ene-1,2-dicarboxylate Chemical compound C(C1C(C(=O)OCC(CCCC)CC)CCC=C1)(=O)OCC(C)C HSRUUIXSSLZEHN-UHFFFAOYSA-N 0.000 claims description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- 150000008064 anhydrides Chemical class 0.000 claims description 3
- HORIEOQXBKUKGQ-UHFFFAOYSA-N bis(7-methyloctyl) cyclohexane-1,2-dicarboxylate Chemical compound CC(C)CCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCC(C)C HORIEOQXBKUKGQ-UHFFFAOYSA-N 0.000 claims description 3
- XRFYGUOAWVKOCQ-UHFFFAOYSA-N bis(8-methylnonyl) cyclohex-4-ene-1,2-dicarboxylate Chemical compound CC(C)CCCCCCCOC(=O)C1CC=CCC1C(=O)OCCCCCCCC(C)C XRFYGUOAWVKOCQ-UHFFFAOYSA-N 0.000 claims description 3
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 claims description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 3
- DHLISFIIKWLXID-UHFFFAOYSA-N 2-o-(2-ethylhexyl) 1-o-(2-methylpropyl) cyclohexane-1,2-dicarboxylate Chemical compound CCCCC(CC)COC(=O)C1CCCCC1C(=O)OCC(C)C DHLISFIIKWLXID-UHFFFAOYSA-N 0.000 claims description 2
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 claims description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 claims description 2
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 claims description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 claims description 2
- 229940098779 methanesulfonic acid Drugs 0.000 claims description 2
- ITNVWQNWHXEMNS-UHFFFAOYSA-N methanolate;titanium(4+) Chemical compound [Ti+4].[O-]C.[O-]C.[O-]C.[O-]C ITNVWQNWHXEMNS-UHFFFAOYSA-N 0.000 claims description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 2
- HKJYVRJHDIPMQB-UHFFFAOYSA-N propan-1-olate;titanium(4+) Chemical compound CCCO[Ti](OCCC)(OCCC)OCCC HKJYVRJHDIPMQB-UHFFFAOYSA-N 0.000 claims description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 2
- 229910001887 tin oxide Inorganic materials 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 description 36
- 238000003860 storage Methods 0.000 description 34
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 26
- 238000000034 method Methods 0.000 description 22
- QDTDKYHPHANITQ-UHFFFAOYSA-N 7-methyloctan-1-ol Chemical compound CC(C)CCCCCCO QDTDKYHPHANITQ-UHFFFAOYSA-N 0.000 description 15
- 230000006837 decompression Effects 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 9
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 238000004040 coloring Methods 0.000 description 8
- 238000011010 flushing procedure Methods 0.000 description 8
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
- 150000005690 diesters Chemical class 0.000 description 7
- 238000004821 distillation Methods 0.000 description 7
- 239000012535 impurity Substances 0.000 description 6
- 239000001361 adipic acid Substances 0.000 description 5
- 235000011037 adipic acid Nutrition 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 239000011261 inert gas Substances 0.000 description 5
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 5
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 5
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 4
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 4
- OAKAPFPXXUWHMV-UHFFFAOYSA-N 2-methoxycarbonylcyclohex-3-ene-1-carboxylic acid Chemical compound COC(=O)C1C=CCCC1C(O)=O OAKAPFPXXUWHMV-UHFFFAOYSA-N 0.000 description 4
- BOVPVRGRPPYECC-UHFFFAOYSA-N 2-methoxycarbonylcyclohexane-1-carboxylic acid Chemical compound COC(=O)C1CCCCC1C(O)=O BOVPVRGRPPYECC-UHFFFAOYSA-N 0.000 description 4
- QVEYQQSQRKMZMZ-UHFFFAOYSA-N CCCCCCCCCCCCCCOC(=O)C1C=CCCC1C(=O)O Chemical compound CCCCCCCCCCCCCCOC(=O)C1C=CCCC1C(=O)O QVEYQQSQRKMZMZ-UHFFFAOYSA-N 0.000 description 4
- 239000002841 Lewis acid Substances 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 4
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 4
- 150000007517 lewis acids Chemical class 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- FJVPOHVUIZGYAJ-UHFFFAOYSA-N 2-(8-methylnonoxycarbonyl)cyclohex-3-ene-1-carboxylic acid Chemical compound CC(C)CCCCCCCOC(=O)C1C=CCCC1C(=O)O FJVPOHVUIZGYAJ-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical class [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 239000006103 coloring component Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- KNDQHSIWLOJIGP-UMRXKNAASA-N (3ar,4s,7r,7as)-rel-3a,4,7,7a-tetrahydro-4,7-methanoisobenzofuran-1,3-dione Chemical compound O=C1OC(=O)[C@@H]2[C@H]1[C@]1([H])C=C[C@@]2([H])C1 KNDQHSIWLOJIGP-UMRXKNAASA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- IKTVAFFOQDDQGF-UHFFFAOYSA-N 1-o-nonyl 2-o-tridecyl cyclohexane-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCCCC IKTVAFFOQDDQGF-UHFFFAOYSA-N 0.000 description 2
- ACBFJMAXNZVRRX-UHFFFAOYSA-N 1-o-nonyl 2-o-undecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC ACBFJMAXNZVRRX-UHFFFAOYSA-N 0.000 description 2
- YPVOJEHTJJVISZ-UHFFFAOYSA-N 1-o-nonyl 2-o-undecyl cyclohexane-1,2-dicarboxylate Chemical compound CCCCCCCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCCCC YPVOJEHTJJVISZ-UHFFFAOYSA-N 0.000 description 2
- RAIHSVAQOXCZBG-UHFFFAOYSA-N 2-(2,2,4-trimethylheptadecan-7-yloxycarbonyl)benzoic acid Chemical compound CCCCCCCCCCC(CCC(C)CC(C)(C)C)OC(=O)C1=CC=CC=C1C(=O)O RAIHSVAQOXCZBG-UHFFFAOYSA-N 0.000 description 2
- LWGSMDGFHGSQRK-UHFFFAOYSA-N 2-(2-methylheptadecan-8-yloxycarbonyl)cyclohexane-1-carboxylic acid Chemical compound CCCCCCCCCC(CCCCCC(C)C)OC(=O)C1CCCCC1C(=O)O LWGSMDGFHGSQRK-UHFFFAOYSA-N 0.000 description 2
- VDGKBWSGLJVZSZ-UHFFFAOYSA-N 2-butoxycarbonylcyclohex-3-ene-1-carboxylic acid Chemical compound CCCCOC(=O)C1C=CCCC1C(O)=O VDGKBWSGLJVZSZ-UHFFFAOYSA-N 0.000 description 2
- SBNWXJRZMRVSGZ-UHFFFAOYSA-N 2-decoxycarbonylcyclohex-3-ene-1-carboxylic acid Chemical compound CCCCCCCCCCOC(=O)C1C=CCCC1C(=O)O SBNWXJRZMRVSGZ-UHFFFAOYSA-N 0.000 description 2
- YVASAEJWOHFMGI-UHFFFAOYSA-N 2-decoxycarbonylcyclohexane-1-carboxylic acid Chemical compound CCCCCCCCCCOC(=O)C1CCCCC1C(O)=O YVASAEJWOHFMGI-UHFFFAOYSA-N 0.000 description 2
- GRNPHLNWVXFPAJ-UHFFFAOYSA-N 2-docosan-10-yloxycarbonyl-2-methylcyclohex-3-ene-1-carboxylic acid Chemical compound CCCCCCCCCCCCC(CCCCCCCCC)OC(=O)C1(C=CCCC1C(=O)O)C GRNPHLNWVXFPAJ-UHFFFAOYSA-N 0.000 description 2
- JZUNESAWBYKDII-UHFFFAOYSA-N 2-henicosan-10-yloxycarbonyl-2-methylcyclohex-3-ene-1-carboxylic acid Chemical compound CCCCCCCCCCCC(CCCCCCCCC)OC(=O)C1(C=CCCC1C(=O)O)C JZUNESAWBYKDII-UHFFFAOYSA-N 0.000 description 2
- WGTNCUSZKDCDAW-UHFFFAOYSA-N 2-icosan-10-yloxycarbonyl-2-methylcyclohex-3-ene-1-carboxylic acid Chemical compound CCCCCCCCCCC(CCCCCCCCC)OC(=O)C1(C=CCCC1C(=O)O)C WGTNCUSZKDCDAW-UHFFFAOYSA-N 0.000 description 2
- MCGQBCVQNUIWMV-UHFFFAOYSA-N 2-methyl-2-tricosan-10-yloxycarbonylcyclohex-3-ene-1-carboxylic acid Chemical compound CCCCCCCCCCCCCC(CCCCCCCCC)OC(=O)C1(C=CCCC1C(=O)O)C MCGQBCVQNUIWMV-UHFFFAOYSA-N 0.000 description 2
- ODGCZQFTJDEYNI-UHFFFAOYSA-N 2-methylcyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1(C)C=CCCC1C(O)=O ODGCZQFTJDEYNI-UHFFFAOYSA-N 0.000 description 2
- AFLFNFIJYCRIOK-UHFFFAOYSA-N 2-nonoxycarbonylcyclohexane-1-carboxylic acid Chemical compound CCCCCCCCCOC(=O)C1CCCCC1C(O)=O AFLFNFIJYCRIOK-UHFFFAOYSA-N 0.000 description 2
- NSZKIDSVINDASL-UHFFFAOYSA-N 2-o-decyl 1-o-nonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC NSZKIDSVINDASL-UHFFFAOYSA-N 0.000 description 2
- LVAGMBHLXLZJKZ-UHFFFAOYSA-N 2-o-decyl 1-o-octyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC LVAGMBHLXLZJKZ-UHFFFAOYSA-N 0.000 description 2
- KITBCBPQQPIMKK-UHFFFAOYSA-N 2-o-dodecyl 1-o-nonyl cyclohexane-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCCCC KITBCBPQQPIMKK-UHFFFAOYSA-N 0.000 description 2
- RYNNDYHGXGHFKB-UHFFFAOYSA-N 2-octadecoxycarbonylcyclohex-3-ene-1-carboxylic acid Chemical compound C(C1C(C(=O)O)CCC=C1)(=O)OCCCCCCCCCCCCCCCCCC RYNNDYHGXGHFKB-UHFFFAOYSA-N 0.000 description 2
- BODRLKRKPXBDBN-UHFFFAOYSA-N 3,5,5-Trimethyl-1-hexanol Chemical compound OCCC(C)CC(C)(C)C BODRLKRKPXBDBN-UHFFFAOYSA-N 0.000 description 2
- DTNRPTWRRFPOIM-UHFFFAOYSA-N 6-(2-methylheptadecan-8-yloxy)-6-oxohexanoic acid Chemical compound CCCCCCCCCC(CCCCCC(C)C)OC(=O)CCCCC(=O)O DTNRPTWRRFPOIM-UHFFFAOYSA-N 0.000 description 2
- XBKNNCFMOICKQC-UHFFFAOYSA-N 6-O-decyl 1-O-nonyl hexanedioate Chemical compound C(CCCCC(=O)OCCCCCCCCCC)(=O)OCCCCCCCCC XBKNNCFMOICKQC-UHFFFAOYSA-N 0.000 description 2
- PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 description 2
- XDCFILGIMITQSO-UHFFFAOYSA-N C(C1C(C(=O)OCCCCCCCCCCCCC)CCC=C1)(=O)OCCCCCCCCC Chemical compound C(C1C(C(=O)OCCCCCCCCCCCCC)CCC=C1)(=O)OCCCCCCCCC XDCFILGIMITQSO-UHFFFAOYSA-N 0.000 description 2
- NKHNZOAIHMSMKX-UHFFFAOYSA-N C(C1C(C(=O)OCCCCCCCCCCCCCC)CCC=C1)(=O)OCCCCCCCCC Chemical compound C(C1C(C(=O)OCCCCCCCCCCCCCC)CCC=C1)(=O)OCCCCCCCCC NKHNZOAIHMSMKX-UHFFFAOYSA-N 0.000 description 2
- FMKDEQASIKRLHG-UHFFFAOYSA-N C(C1C(C(=O)OCCCCCCCCCCCCCCCCCC)CCC=C1)(=O)OCCCCCCCCC Chemical compound C(C1C(C(=O)OCCCCCCCCCCCCCCCCCC)CCC=C1)(=O)OCCCCCCCCC FMKDEQASIKRLHG-UHFFFAOYSA-N 0.000 description 2
- BEGBVVOCVNYABJ-UHFFFAOYSA-N CC(C)COC(C(CCC=C1)C1(C)C(OCC(C)C)=O)=O Chemical compound CC(C)COC(C(CCC=C1)C1(C)C(OCC(C)C)=O)=O BEGBVVOCVNYABJ-UHFFFAOYSA-N 0.000 description 2
- ZJDSDRLWTRIJFZ-UHFFFAOYSA-N CCCCCCCCCCCCCCCCCCOC(C1=CC=CC=C1C(OCCCCCCC(C)C)=O)=O Chemical compound CCCCCCCCCCCCCCCCCCOC(C1=CC=CC=C1C(OCCCCCCC(C)C)=O)=O ZJDSDRLWTRIJFZ-UHFFFAOYSA-N 0.000 description 2
- HNUZAMUPCKRAFI-UHFFFAOYSA-N CCCCCCCCCCCCCCOC(=O)C1CCC=CC1C(=O)OCCCCCCCCCCCCCC Chemical compound CCCCCCCCCCCCCCOC(=O)C1CCC=CC1C(=O)OCCCCCCCCCCCCCC HNUZAMUPCKRAFI-UHFFFAOYSA-N 0.000 description 2
- SFRPPKYCNAJOQO-UHFFFAOYSA-N CCCCCCCCCCCCOC(C1=CC=CC=C1C(OCCCCCCC(C)C)=O)=O Chemical compound CCCCCCCCCCCCOC(C1=CC=CC=C1C(OCCCCCCC(C)C)=O)=O SFRPPKYCNAJOQO-UHFFFAOYSA-N 0.000 description 2
- KVQPXHHEFCCUIX-UHFFFAOYSA-N CCCCCCCCCOC(=O)C1C=CCCC1C(=O)O Chemical compound CCCCCCCCCOC(=O)C1C=CCCC1C(=O)O KVQPXHHEFCCUIX-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- 238000005698 Diels-Alder reaction Methods 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
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- GYFBKUFUJKHFLZ-UHFFFAOYSA-N dioctadecyl hexanedioate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCCCCCCCC GYFBKUFUJKHFLZ-UHFFFAOYSA-N 0.000 description 1
- NSTQBBLISXXLSM-UHFFFAOYSA-N dioctyl 1-methylcyclohexane-1,2-dicarboxylate Chemical compound CCCCCCCCOC(=O)C1CCCCC1(C)C(=O)OCCCCCCCC NSTQBBLISXXLSM-UHFFFAOYSA-N 0.000 description 1
- FUXJJBJXVZIIMV-UHFFFAOYSA-N dioctyl cyclohexane-1,2-dicarboxylate Chemical compound CCCCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCCC FUXJJBJXVZIIMV-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- RBYVYSLRBYOECN-UHFFFAOYSA-N ditetradecyl 1-methylcyclohexane-1,2-dicarboxylate Chemical compound CC1(C(=O)OCCCCCCCCCCCCCC)C(C(=O)OCCCCCCCCCCCCCC)CCCC1 RBYVYSLRBYOECN-UHFFFAOYSA-N 0.000 description 1
- IELTYMMIWIGNKN-UHFFFAOYSA-N ditetradecyl 2-methylcyclohex-3-ene-1,2-dicarboxylate Chemical compound CC1(C(=O)OCCCCCCCCCCCCCC)C(C(=O)OCCCCCCCCCCCCCC)CCC=C1 IELTYMMIWIGNKN-UHFFFAOYSA-N 0.000 description 1
- UVXWTPCEYFWVDZ-UHFFFAOYSA-N ditetradecyl cyclohexane-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCCCCCCCCC UVXWTPCEYFWVDZ-UHFFFAOYSA-N 0.000 description 1
- QZQPCVVMCYMSFX-UHFFFAOYSA-N ditetradecyl hexanedioate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCCCC QZQPCVVMCYMSFX-UHFFFAOYSA-N 0.000 description 1
- KXMMAQISHMLTHI-UHFFFAOYSA-N ditridecyl 1-methylcyclohexane-1,2-dicarboxylate Chemical compound CC1(C(=O)OCCCCCCCCCCCCC)C(C(=O)OCCCCCCCCCCCCC)CCCC1 KXMMAQISHMLTHI-UHFFFAOYSA-N 0.000 description 1
- YCZJVRCZIPDYHH-UHFFFAOYSA-N ditridecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCC YCZJVRCZIPDYHH-UHFFFAOYSA-N 0.000 description 1
- QBNKOOBQDPEETD-UHFFFAOYSA-N ditridecyl cyclohexane-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCCCCCCCC QBNKOOBQDPEETD-UHFFFAOYSA-N 0.000 description 1
- LZJUZSYHFSVIGJ-UHFFFAOYSA-N ditridecyl hexanedioate Chemical compound CCCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCCC LZJUZSYHFSVIGJ-UHFFFAOYSA-N 0.000 description 1
- QQVHEQUEHCEAKS-UHFFFAOYSA-N diundecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCC QQVHEQUEHCEAKS-UHFFFAOYSA-N 0.000 description 1
- OACQFHLGZUHNQE-UHFFFAOYSA-N diundecyl cyclohexane-1,2-dicarboxylate Chemical compound CCCCCCCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCCCCCC OACQFHLGZUHNQE-UHFFFAOYSA-N 0.000 description 1
- WIZIPYVLMUMDQT-UHFFFAOYSA-N diundecyl hexanedioate Chemical compound CCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCC WIZIPYVLMUMDQT-UHFFFAOYSA-N 0.000 description 1
- TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical compound O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- XVQUOJBERHHONY-UHFFFAOYSA-N isometheptene Chemical group CNC(C)CCC=C(C)C XVQUOJBERHHONY-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- VYKXQOYUCMREIS-UHFFFAOYSA-N methylhexahydrophthalic anhydride Chemical compound C1CCCC2C(=O)OC(=O)C21C VYKXQOYUCMREIS-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- DFFZOPXDTCDZDP-UHFFFAOYSA-N naphthalene-1,5-dicarboxylic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1C(O)=O DFFZOPXDTCDZDP-UHFFFAOYSA-N 0.000 description 1
- JSKSILUXAHIKNP-UHFFFAOYSA-N naphthalene-1,7-dicarboxylic acid Chemical compound C1=CC=C(C(O)=O)C2=CC(C(=O)O)=CC=C21 JSKSILUXAHIKNP-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- ZJHUBLNWMCWUOV-UHFFFAOYSA-N oxocane-2,8-dione Chemical compound O=C1CCCCCC(=O)O1 ZJHUBLNWMCWUOV-UHFFFAOYSA-N 0.000 description 1
- JQCXWCOOWVGKMT-UHFFFAOYSA-N phthalic acid diheptyl ester Natural products CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- RLJWTAURUFQFJP-UHFFFAOYSA-N propan-2-ol;titanium Chemical compound [Ti].CC(C)O.CC(C)O.CC(C)O.CC(C)O RLJWTAURUFQFJP-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 150000003608 titanium Chemical class 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000003799 water insoluble solvent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
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- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Description
本発明に用いられる原料アルコールとしては、そのままアルコール原料として使用しても色相の優れたジカルボン酸ジエステルが得られない熱及び/又は酸化劣化した低品質原料アルコールが例示される。
タル酸ジイソブチル、メチルテトラヒドロフタル酸イソブチル2−エチルヘキシル、メチルテトラヒドロフタル酸イソブチルn−オクチル、メチルテトラヒドロフタル酸イソブチルn−ノニル、メチルテトラヒドロフタル酸イソブチルイソノニル、メチルテトラヒドロフタル酸イソブチル3,5,5−トリメチルヘキシル、メチルテトラヒドロフタル酸イソブチルn−デシル、メチルテトラヒドロフタル酸イソブチルイソデシル、メチルテトラヒドロフタル酸イソブチルウンデシル、メチルテトラヒドロフタル酸イソブチルドデシル、メチルテトラヒドロフタル酸イソブチルトリデシル、メチルテトラヒドロフタル酸イソブチルテトラデシル、メチルテトラヒドロフタル酸イソブチルオクタデシル、メチルテトラヒドロフタル酸n−オクチルn−ノニル、メチルテトラヒドロフタル酸n−オクチルイソノニル、メチルテトラヒドロフタル酸n−オクチル3,5,5−トリメチルヘキシル、メチルテトラヒドロフタル酸n−オクチルn−デシル、メチルテトラヒドロフタル酸n−オクチルイソデシル、メチルテトラヒドロフタル酸n−オクチルウンデシル、メチルテトラヒドロフタル酸n−オクチルドデシル、メチルテトラヒドロフタル酸n−オクチルトリデシル、メチルテトラヒドロフタル酸n−オクチルテトラデシル、メチルテトラヒドロフタル酸n−オクチルオクタデシル、メチルテトラヒドロフタル酸n−ノニルイソノニル、メチルテトラヒドロフタル酸n−ノニル3,5,5−トリメチルヘキシル、メチルテトラヒドロフタル酸n−ノニルn−デシル、メチルテトラヒドロフタル酸n−ノニルイソデシル、メチルテトラヒドロフタル酸n−ノニルウンデシル、メチルテトラヒドロフタル酸n−ノニルドデシル、メチルテトラヒドロフタル酸n−ノニルトリデシル、メチルテトラヒドロフタル酸n−ノニルテトラデシル、メチルテトラヒドロフタル酸n−ノニルオクタデシル、メチルテトラヒドロフタル酸n−ノニルイソノニル、メチルテトラヒドロフタル酸n−ノニル3,5,5−トリメチルヘキシル、メチルテトラヒドロフタル酸n−ノニルn−デシル、メチルテトラヒドロフタル酸n−ノニルイソデシル、メチルテトラヒドロフタル酸n−ノニルウンデシル、メチルテトラヒドロフタル酸n−ノニルドデシル、メチルテトラヒドロフタル酸n−ノニルトリデシル、メチルテトラヒドロフタル酸n−ノニルテトラデシル、メチルテトラヒドロフタル酸n−ノニルオクタデシル、メチルテトラヒドロフタル酸イソノニル3,5,5−トリメチルヘキシル、メチルテトラヒドロフタル酸イソノニルn−デシル、メチルテトラヒドロフタル酸イソノニルイソデシル、メチルテトラヒドロフタル酸イソノニルウンデシル、メチルテトラヒドロフタル酸イソノニルドデシル、メチルテトラヒドロフタル酸イソノニルトリデシル、メチルテトラヒドロフタル酸イソノニルテトラデシル、メチルテトラヒドロフタル酸イソノニルオクタデシル、メチルテトラヒドロフタル酸3,5,5−トリメチルヘキシルn−デシル、メチルテトラヒドロフタル酸3,5,5−トリメチルヘキシルイソデシル、メチルテトラヒドロフタル酸3,5,5−トリメチルヘキシルウンデシル、メチルテトラヒドロフタル酸3,5,5−トリメチルヘキシルドデシル、メチルテトラヒドロフタル酸3,5,5−トリメチルヘキシルトリデシル、メチルテトラヒドロフタル酸3,5,5−トリメチルヘキシルテトラデシル、メチルテトラヒドロフタル酸3,5,5−トリメチルヘキシルオクタデシル、メチルテトラヒドロフタル酸n−デシルイソデシル、メチルテトラヒドロフタル酸n−デシルウンデシル、メチルテトラヒドロフタル酸n−デシルドデシル、メチルテトラヒドロフタル酸n−デシルトリデシル、メチルテトラヒドロフタル酸n−デシルテトラデシル、メチルテトラヒドロフタル酸n−デシルオクタデシル、メチルテトラヒドロフタル酸イソデシルウンデシル、メチルテトラヒドロフタル酸イソデシルドデシル、メチルテトラヒドロフタル酸イソデシルトリデシル、メチルテトラヒドロフタル酸イソデシルテトラデシル、メチルテトラヒドロフタル酸イソデシルオクタデシル、メチルテトラヒドロフタル酸ウンデシルドデシル、メチルテトラヒドロフタル酸ウンデシルトリデシル、メチルテトラヒドロフタル酸ウンデシルテトラデシル、メチルテトラヒドロフタル酸ウンデシルオクタデシル、メチルテトラヒドロフタル酸ドデシルトリデシル、メチルテトラヒドロフタル酸ドデシルテトラデシル、メチルテトラヒドロフタル酸ドデシルオクタデシル、メチルテトラヒドロフタル酸トリデシルテトラデシル、メチルテトラヒドロフタル酸トリデシルオクタデシル、メチルテトラヒドロフタル酸テトラデシルオクタデシル、メチルヘキサヒドロフタル酸ジn−ブチル、メチルヘキサヒドロフタル酸n−ブチル2−エチルヘキシル、メチルヘキサヒドロフタル酸ジ2−エチルヘキシル、メチルヘキサヒドロフタル酸n−ブチルn−オクチル、メチルヘキサヒドロフタル酸ジn−オクチル、メチルヘキサヒドロフタル酸n−ブチルn−ノニル、メチルヘキサヒドロフタル酸ジn−ノニル、メチルヘキサヒドロフタル酸n−ブチルイソノニル、メチルヘキサヒドロフタル酸ジイソノニル、メチルヘキサヒドロフタル酸n−ブチル3,5,5−トリメチルヘキシル、メチルヘキサヒドロフタル酸ジ3,5,5−トリメチルヘキシル、メチルヘキサヒドロフタル酸n−ブチルn−デシル、メチルヘキサヒドロフタル酸ジn−デシル、メチルヘキサヒドロフタル酸n−ブチルイソデシル、メチルヘキサヒドロフタル酸ジイソデシル、メチルヘキサヒドロフタル酸n−ブチルウンデシル、メチルヘキサヒドロフタル酸ジウンデシル、メチルヘキサヒドロフタル酸n−ブチルドデシル、メチルヘキサヒドロフタル酸ジドデシル、メチルヘキサヒドロフタル酸n−ブチルトリデシル、メチルヘキサヒドロフタル酸ジトリデシル、メチルヘキサヒドロフタル酸n−ブチルテトラデシル、メチルヘキサヒドロフタル酸ジテトラデシル、メチルヘキサヒドロフタル酸n−ブチルオクタデシル、メチルヘキサヒドロフタル酸ジオクタデシル、メチルヘキサヒドロフタル酸ジイソブチル、メチルヘキサヒドロフタル酸イソブチル2−エチルヘキシル、メチルヘキサヒドロフタル酸イソブチルn−オクチル、メチルヘキサヒドロフタル酸イソブチルn−ノニル、メチルヘキサヒドロフタル酸イソブチルイソノニル、メチルヘキサヒドロフタル酸イソブチル3,5,5−トリメチルヘキシル、メチルヘキサヒドロフタル酸イソブチルn−デシル、メチルヘキサヒドロフタル酸イソブチルイソデシル、メチルヘキサヒドロフタル酸イソブチルウンデシル、メチルヘキサヒドロフタル酸イソブチルドデシル、メチルヘキサヒドロフタル酸イソブチルトリデシル、メチルヘキサヒドロフタル酸イソブチルテトラデシル、メチルヘキサヒドロフタル酸イソブチルオクタデシル、メチルヘキサヒドロフタル酸n−オクチルn−ノニル、メチルヘキサヒドロフタル酸n−オクチルイソノニル、メチルヘキサヒドロフタル酸n−オクチル3,5,5−トリメチルヘキシル、メチルヘキサヒドロフタル酸n−オクチルn−デシル、メチルヘキサヒドロフタル酸n−オクチルイソデシル、メチルヘキサヒドロフタル酸n−オクチルウンデシル、メチルヘキサヒドロフタル酸n−オクチルドデシル、メチルヘキサヒドロフタル酸n−オクチルトリデシル、メチルヘキサヒドロフタル酸n−オクチルテトラデシル、メチルヘキサヒドロフタル酸n−オクチルオクタデシル、メチルヘキサヒドロフタル酸n−ノニルイソノニル、メチルヘキサヒドロフタル酸n−ノニル3,5,5−トリメチルヘキシル、メチルヘキサヒドロフタル酸n−ノニルn−デシル、メチルヘキサヒドロフタル酸n−ノニルイソデシル、メチルヘキサヒドロフタル酸n−ノニルウンデシル、メチルヘキサヒドロフタル酸n−ノニルドデシル、メチルヘキサヒドロフタル酸n−ノニルトリデシル、メチルヘキサヒドロフタル酸n−ノニルテトラデシル、メチルヘキサヒドロフタル酸n−ノニルオクタデシル、メチルヘキサヒドロフタル酸n−ノニルイソノニル、メチルヘキサヒドロフタル酸n−ノニル3,5,5−トリメチルヘキシル、メチルヘキサヒドロフタル酸n−ノニルn−デシル、メチルヘキサヒドロフタル酸n−ノニルイソデシル、メチルヘキサヒドロフタル酸n−ノニルウンデシル、メチルヘキサヒドロフタル酸n−ノニルドデシル、メチルヘキサヒドロフタル酸n−ノニルトリデシル、メチルヘキサヒドロフタル酸n−ノニルテトラデシル、メチルヘキサヒドロフタル酸n−ノニルオクタデシル、メチルヘキサヒドロフタル酸イソノニル3,5,5−トリメチルヘキシル、メチルヘキサヒドロフタル酸イソノニルn−デシル、メチルヘキサヒドロフタル酸イソノニルイソデシル、メチルヘキサヒドロフタル酸イソノニルウンデシル、メチルヘキサヒドロフタル酸イソノニルドデシル、メチルヘキサヒドロフタル酸イソノニルトリデシル、メチルヘキサヒドロフタル酸イソノニルテトラデシル、メチルヘキサヒドロフタル酸イソノニルオクタデシル、メチルヘキサヒドロフタル酸3,5,5−トリメチルヘキシルn−デシル、メチルヘキサヒドロフタル酸3,5,5−トリメチルヘキシルイソデシル、メチルヘキサヒドロフタル酸3,5,5−トリメチルヘキシルウンデシル、メチルヘキサヒドロフタル酸3,5,5−トリメチルヘキシルドデシル、メチルヘキサヒドロフタル酸3,5,5−トリメチルヘキシルトリデシル、メチルヘキサヒドロフタル酸3,5,5−トリメチルヘキシルテトラデシル、メチルヘキサヒドロフタル酸3,5,5−トリメチルヘキシルオクタデシル、メチルヘキサヒドロフタル酸n−デシルイソデシル、メチルヘキサヒドロフタル酸n−デシルウンデシル、メチルヘキサヒドロフタル酸n−デシルドデシル、メチルヘキサヒドロフタル酸n−デシルトリデシル、メチルヘキサヒドロフタル酸n−デシルテトラデシル、メチルヘキサヒドロフタル酸n−デシルオクタデシル、メチルヘキサヒドロフタル酸イソデシルウンデシル、メチルヘキサヒドロフタル酸イソデシルドデシル、メチルヘキサヒドロフタル酸イソデシルトリデシル、メチルヘキサヒドロフタル酸イソデシルテトラデシル、メチルヘキサヒドロフタル酸イソデシルオクタデシル、メチルヘキサヒドロフタル酸ウンデシルドデシル、メチルヘキサヒドロフタル酸ウンデシルトリデシル、メチルヘキサヒドロフタル酸ウンデシルテトラデシル、メチルヘキサヒドロフタル酸ウンデシルオクタデシル、メチルヘキサヒドロフタル酸ドデシルトリデシル、メチルヘキサヒドロフタル酸ドデシルテトラデシル、メチルヘキサヒドロフタル酸ドデシルオクタデシル、メチルヘキサヒドロフタル酸トリデシルテトラデシル、メチルヘキサヒドロフタル酸トリデシルオクタデシル、メチルヘキサヒドロフタル酸テトラデシルオクタデシル等の脂環式ジカルボン酸ジエステルが挙げられる。
JIS K 1525に記載の方法に準拠し測定した。
(2)過酸化物価(POV)
基準油脂分析試験法に記載の方法に準拠して測定した。
(3)硫酸呈色
濃硫酸で洗浄し、更に蒸留水ですすぎを行い、乾燥後の300mlの共栓付き平底フラスコに試料200mlを入れ、マグネティックスターラーで撹拌しながら氷浴で30℃以下の温度で98wt%の濃硫酸17.5mlを25mlビュレットにて3.5ml/分の速度で加える。共栓をして98±2℃のオイルバスに1時間浸す。冷却後試料の色相(ハーゼン)をJIS K−0071の方法に準拠して測定した。
(4)色相(ハーゼン)
ジカルボン酸ジエステルの色相はJIS K−0071の方法で測定した。
さらに、実施例1において、COVが0.38mgKOH/g、POVが5.22meq/kgの回収2−エチルヘキサノールを用いた以外は実施例1と同様の処理を行ったところ得られたカルボン酸ジエステルの色相は15であった。
さらに、実施例6において、COVが0.42mgKOH/g、POVが7.44meq/kgの回収イソノナノールを用いた以外は実施例6と同様の処理を行ったところ得られたカルボン酸ジエステルの色相は15であった。
実施例1においてアルコールのフラッシュ処理を行わずに、実施例1と同様にジエステル化のみを行ったところ、得られたジカルボン酸ジエステルの色相は30であった。
実施例1においてアルコールにCOV0.04mgKOH/g、POVは0.27meq/kg、硫酸呈色がハーゼンで20の2−エチルヘキサノールを用い、フラッシュ処理を行わずに、実施例1と同様にジエステル化のみを行ったところ、得られたジカルボン酸ジエステルの色相は10であった。
実施例6においてアルコールのフラッシュ処理を行わずに、実施例1と同様にジエステル化のみを行ったところ、得られたジカルボン酸ジエステルの色相は40であった。
実施例1において原料アルコールにCOV0.09mgKOH/g、POVは0.78meq/kg、硫酸呈色がハーゼンで10のイソノナノールを用い、フラッシュ処理を行わずに、実施例1と同様にジエステル化のみを行ったところ、得られたジカルボン酸ジエステルの色相は10であった。
実施例6においてアルコールの加熱ユニット1の出口温度を180℃、減圧チャンバー6内の圧力を4.0×103Paに変えてフラッシュ処理を行ったところ、アルコール回収貯槽8内に得られたイソノナノールは2.88kg、着色成分回収貯槽11には0.12kgで歩留まりは96.0%であった。さらに実施例1と同様にジエステル化を行ったところ、得られたジカルボン酸ジエステルの色相は30であった。
実施例6においてアルコールの加熱ユニット1の出口温度を165℃、減圧チャンバー6内の圧力を2.0×103Paに変えてフラッシュ処理を行ったところ、アルコール回収貯槽8内に得られたイソノナノールは2.83kg、着色成分回収貯槽11には0.17kgで歩留まりは94.3%であった。さらに実施例1と同様にジエステル化を行ったところ、得られたジカルボン酸ジエステルの色相は10であった。
実施例6において減圧チャンバー6内の圧力を26.7×103Paに変えてフラッシュ処理を行ったところ、アルコール回収貯槽8内に得られたイソノナノールは2.99kg、着色成分回収貯槽11には0.01kgで歩留まりは99.7%であった。さらに実施例1と同様にジエステル化を行ったところ、得られたジカルボン酸ジエステルの色相は40であった。
比較例3において無水フタル酸の代わりにテトラヒドロフタル酸無水物76.0g(0.5モル)を用いて実施例1と同様にジエステル化を行ったところ、得られたジカルボン酸ジエステルの色相は40であった。
実施例3において無水フタル酸の代わりにヘキサヒドロフタル酸無水物77.0g(0.5モル)を用いて実施例1と同様にジエステル化を行ったところ、得られたジカルボン酸ジエステルの色相は30であった。
実施例3において無水フタル酸の代わりにアジピン酸73.0g(0.5モル)を用いて実施例1と同様にジエステル化を行ったところ、得られたジカルボン酸ジエステルの色相は40であった。
2・・・ポンプ
3・・・加熱チャンバー
4・・・コイル式加熱管
5・・・原料アルコール回収ユニット
6・・・減圧チャンバー
7・・・目皿式分散板
8・・・アルコール回収貯相
9・・・着色原因成分捕集ユニット
10・・・コンデンサ
11・・・着色原因成分回収貯槽
12・・・真空ポンプ
Claims (5)
- ジカルボン酸又はその無水物とアルコールとをパラトルエンスルホン酸、メタンスルホン酸、硫酸、テトラメチルチタネート、テトラエチルチタネート、テトラ−n−プロピルチタネート、テトライソプロピルチタネート、テトラ−n−ブチルチタネート、ジブチル錫ジラウレート、ジブチル錫オキサイド、ジブチル錫ジアセテート、オクチル酸錫及び酸化錫から選ばれるエステル化触媒存在下にエステル化反応させジカルボン酸ジエステルを製造する方法であって、カルボニル価が0.1〜1.0mgKOH/gであり、過酸化物価が0.5〜10.0meq/kgであり、硫酸呈色がハーゼン30〜250の原料アルコールを温度80〜165℃に加熱し、その原料アルコールをフラッシュ缶の缶内圧力4.0×10 3 〜13.3×10 3 Paでフラッシュ蒸発させて得られる該アルコールを用いることを特徴とするジカルボン酸ジエステルの製造方法。
- 原料アルコールが、ジカルボン酸ジエステルの製造の際に発生する回収アルコールを含有する請求項1に記載の製造方法。
- エステル化反応の直前に原料アルコールをフラッシュ蒸発させる、請求項1又は請求項2に記載の製造方法。
- フラッシュ蒸発させる工程における蒸発量が、原料アルコールに対して、0.5〜5重量%となるよう原料アルコールをフラッシュ蒸発させる、請求項1〜3のいずれかに記載の製造方法。
- ジカルボン酸ジエステルが、フタル酸ジ2−エチルヘキシル、フタル酸ジイソノニル、フタル酸ジイソデシル、フタル酸イソブチル2−エチルヘキシル、フタル酸イソブチルイソノニル、テトラヒドロフタル酸ジ2−エチルヘキシル、テトラヒドロフタル酸ジイソノニル、テトラヒドロフタル酸ジイソデシル、テトラヒドロフタル酸イソブチル2−エチルヘキシル、テトラヒドロフタル酸イソブチルイソノニル、ヘキサヒドロフタル酸ジ2−エチルヘキシル、ヘキサヒドロフタル酸ジイソノニル、ヘキサヒドロフタル酸ジイソデシル、ヘキサヒドロフタル酸イソブチル2−エチルヘキシル、又はヘキサヒドロフタル酸イソブチルイソノニルである請求項1〜4のいずれかに記載のジカルボン酸ジエステルの製造方法。
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KR20210025808A (ko) * | 2019-08-28 | 2021-03-10 | 주식회사 거영 | 디부틸 테트라하이드로프탈레이트의 제조방법 및 이로부터 제조된 디부틸 테트라하이드로프탈레이트 |
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EP1953135A1 (en) * | 2007-02-05 | 2008-08-06 | Nan Ya Plastics Corporation | Method of preparing cyclohexanepolycarobxylic acid ester without phthalatic and plasticizer prepared by the same |
JP2008239582A (ja) * | 2007-03-28 | 2008-10-09 | Nan Ya Plast Corp | フタル酸非含有シクロヘキサンポリカルボン酸エステルの調製方法及びそれにより調製した可塑剤 |
JP5245298B2 (ja) * | 2007-06-15 | 2013-07-24 | 川崎化成工業株式会社 | リンゴ酸ジアルキルエステル及びその製造方法 |
CA2908710A1 (en) | 2013-05-20 | 2014-11-27 | Saudi Basic Industries Corporation | Method for the purification of acetic acid and acrylic acid |
AU2014276475B2 (en) | 2013-06-07 | 2017-01-12 | Saudi Basic Industries Corporation | Method for purifying dioctyl phthalate |
KR101939160B1 (ko) * | 2015-05-14 | 2019-01-16 | 주식회사 엘지화학 | 에스테르계 화합물, 이를 포함하는 조성물, 이의 제조방법, 및 이를 포함하는 수지 조성물 |
CN111073440B (zh) * | 2019-12-02 | 2021-11-30 | 昆山爱克树脂有限公司 | 一种能够除甲醛的建筑用装饰涂料及其制备方法 |
CN114605258B (zh) * | 2022-02-24 | 2023-12-15 | 丹阳市助剂化工厂有限公司 | 一种高产邻苯二甲酸二异丁酯制备方法 |
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KR102356046B1 (ko) * | 2019-08-28 | 2022-01-26 | 주식회사 거영 | 디부틸 테트라하이드로프탈레이트의 제조방법 및 이로부터 제조된 디부틸 테트라하이드로프탈레이트 |
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