JP6720913B2 - 不飽和結合含有ビスシリル化合物およびその製造方法 - Google Patents
不飽和結合含有ビスシリル化合物およびその製造方法 Download PDFInfo
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- JP6720913B2 JP6720913B2 JP2017081700A JP2017081700A JP6720913B2 JP 6720913 B2 JP6720913 B2 JP 6720913B2 JP 2017081700 A JP2017081700 A JP 2017081700A JP 2017081700 A JP2017081700 A JP 2017081700A JP 6720913 B2 JP6720913 B2 JP 6720913B2
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- Prior art keywords
- dimethylvinylsilyl
- unsaturated bond
- carbon atoms
- atom
- bis
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims description 36
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 25
- -1 amine compound Chemical class 0.000 claims description 23
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 17
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 14
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 12
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 11
- 150000002430 hydrocarbons Chemical group 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 239000007983 Tris buffer Substances 0.000 description 8
- 125000000524 functional group Chemical group 0.000 description 8
- 239000003607 modifier Substances 0.000 description 7
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 125000005842 heteroatom Chemical group 0.000 description 6
- 238000002329 infrared spectrum Methods 0.000 description 6
- 230000004048 modification Effects 0.000 description 6
- 238000012986 modification Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000001294 propane Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 5
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 5
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 5
- 229920000098 polyolefin Polymers 0.000 description 5
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- RHXBJEHRDMJSAG-UHFFFAOYSA-N N,N,N',N'-tetraethyl-1-[2-(2-methylprop-1-enylsilyl)ethylsilyl]methanediamine Chemical compound CC(=C[SiH2]CC[SiH2]C(N(CC)CC)N(CC)CC)C RHXBJEHRDMJSAG-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 238000001819 mass spectrum Methods 0.000 description 4
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 4
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical group CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- PAVVLKKFDHAYME-UHFFFAOYSA-N N-[diethylamino-[2-[[ethenyl(dimethyl)silyl]oxy-dimethylsilyl]ethyl]-methylsilyl]-N-ethylethanamine Chemical compound C(=C)[Si](O[Si](CC[Si](N(CC)CC)(N(CC)CC)C)(C)C)(C)C PAVVLKKFDHAYME-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 3
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000012433 hydrogen halide Substances 0.000 description 3
- 229910000039 hydrogen halide Inorganic materials 0.000 description 3
- 229940098779 methanesulfonic acid Drugs 0.000 description 3
- 125000004430 oxygen atom Chemical group O* 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 2
- 125000003386 piperidinyl group Chemical group 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 125000004434 sulfur atom Chemical group 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- IPFUYZQNYKZRDS-UHFFFAOYSA-N 2-(2-methylprop-1-enylsilyl)ethyl-trimorpholin-4-ylsilane Chemical compound CC(=C[SiH2]CC[Si](N1CCOCC1)(N1CCOCC1)N1CCOCC1)C IPFUYZQNYKZRDS-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- AACXKYQXVGVXGE-UHFFFAOYSA-N 2-[diiodo(methyl)silyl]ethyl-[ethenyl(dimethyl)silyl]oxy-dimethylsilane Chemical compound C(=C)[Si](O[Si](CC[Si](I)(I)C)(C)C)(C)C AACXKYQXVGVXGE-UHFFFAOYSA-N 0.000 description 1
- FRCQJOOGTPYQHV-UHFFFAOYSA-N 2-[dimethyl(morpholin-4-yl)silyl]ethyl-[ethenyl(dimethyl)silyl]oxy-dimethylsilane Chemical compound C(=C)[Si](O[Si](CC[Si](N1CCOCC1)(C)C)(C)C)(C)C FRCQJOOGTPYQHV-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- CTZOSVFZWMDVRL-UHFFFAOYSA-N 2-silylethyl(silyloxy)silane Chemical compound [SiH3]CC[SiH2]O[SiH3] CTZOSVFZWMDVRL-UHFFFAOYSA-N 0.000 description 1
- XREQGSSLHLIPDH-UHFFFAOYSA-N 3-(2-methylprop-1-enylsilyl)propyl-trimorpholin-4-ylsilane Chemical compound CC(=C[SiH2]CCC[Si](N1CCOCC1)(N1CCOCC1)N1CCOCC1)C XREQGSSLHLIPDH-UHFFFAOYSA-N 0.000 description 1
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 description 1
- RGANRAZACTWQNK-UHFFFAOYSA-N 8-(2-methylprop-1-enylsilyl)octyl-trimorpholin-4-ylsilane Chemical compound CC(=C[SiH2]CCCCCCCC[Si](N1CCOCC1)(N1CCOCC1)N1CCOCC1)C RGANRAZACTWQNK-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- SAIKULLUBZKPDA-UHFFFAOYSA-N Bis(2-ethylhexyl) amine Chemical compound CCCCC(CC)CNCC(CC)CCCC SAIKULLUBZKPDA-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical compound C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- YPOSUKITWUSSRS-UHFFFAOYSA-N N,N,N',N'-tetrabutyl-1-(2-methylprop-1-enylsilylmethylsilyl)methanediamine Chemical compound CC(=C[SiH2]C[SiH2]C(N(CCCC)CCCC)N(CCCC)CCCC)C YPOSUKITWUSSRS-UHFFFAOYSA-N 0.000 description 1
- ATPQNJPYXCEHHK-UHFFFAOYSA-N N,N,N',N'-tetrabutyl-1-[2-(2-methylprop-1-enylsilyl)ethylsilyl]methanediamine Chemical compound CC(=C[SiH2]CC[SiH2]C(N(CCCC)CCCC)N(CCCC)CCCC)C ATPQNJPYXCEHHK-UHFFFAOYSA-N 0.000 description 1
- JXPVOGQJLHLHGJ-UHFFFAOYSA-N N,N,N',N'-tetrabutyl-1-[3-(2-methylprop-1-enylsilyl)propylsilyl]methanediamine Chemical compound CC(=C[SiH2]CCC[SiH2]C(N(CCCC)CCCC)N(CCCC)CCCC)C JXPVOGQJLHLHGJ-UHFFFAOYSA-N 0.000 description 1
- DWTYHHSWUGLKLD-UHFFFAOYSA-N N,N,N',N'-tetrabutyl-1-[8-(2-methylprop-1-enylsilyl)octylsilyl]methanediamine Chemical compound CC(=C[SiH2]CCCCCCCC[SiH2]C(N(CCCC)CCCC)N(CCCC)CCCC)C DWTYHHSWUGLKLD-UHFFFAOYSA-N 0.000 description 1
- ZVJMSVRFYCWAGQ-UHFFFAOYSA-N N,N,N',N'-tetraethyl-1-[8-(2-methylprop-1-enylsilyl)octylsilyl]methanediamine Chemical compound CC(=C[SiH2]CCCCCCCC[SiH2]C(N(CC)CC)N(CC)CC)C ZVJMSVRFYCWAGQ-UHFFFAOYSA-N 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- CRVZATQDIYJZDA-UHFFFAOYSA-N N-[2-[[ethenyl(dimethyl)silyl]oxy-dimethylsilyl]ethyl-dimethylsilyl]-N-ethylethanamine Chemical compound C(=C)[Si](O[Si](CC[Si](N(CC)CC)(C)C)(C)C)(C)C CRVZATQDIYJZDA-UHFFFAOYSA-N 0.000 description 1
- FQPQYBNGLLSPJZ-UHFFFAOYSA-N N-[bis(dibutylamino)-(2-methylprop-1-enylsilylmethyl)silyl]-N-butylbutan-1-amine Chemical compound CC(=C[SiH2]C[Si](N(CCCC)CCCC)(N(CCCC)CCCC)N(CCCC)CCCC)C FQPQYBNGLLSPJZ-UHFFFAOYSA-N 0.000 description 1
- APXOQDBQLZHVLG-UHFFFAOYSA-N N-[bis(dibutylamino)-[2-(2-methylprop-1-enylsilyl)ethyl]silyl]-N-butylbutan-1-amine Chemical compound CC(=C[SiH2]CC[Si](N(CCCC)CCCC)(N(CCCC)CCCC)N(CCCC)CCCC)C APXOQDBQLZHVLG-UHFFFAOYSA-N 0.000 description 1
- QOHBKZHSQMMIJR-UHFFFAOYSA-N N-[bis(dibutylamino)-[2-[[ethenyl(dimethyl)silyl]oxy-dimethylsilyl]ethyl]silyl]-N-butylbutan-1-amine Chemical compound C(=C)[Si](O[Si](CC[Si](N(CCCC)CCCC)(N(CCCC)CCCC)N(CCCC)CCCC)(C)C)(C)C QOHBKZHSQMMIJR-UHFFFAOYSA-N 0.000 description 1
- GZVDUOIEQXSAQS-UHFFFAOYSA-N N-[bis(dibutylamino)-[3-(2-methylprop-1-enylsilyl)propyl]silyl]-N-butylbutan-1-amine Chemical compound CC(=C[SiH2]CCC[Si](N(CCCC)CCCC)(N(CCCC)CCCC)N(CCCC)CCCC)C GZVDUOIEQXSAQS-UHFFFAOYSA-N 0.000 description 1
- FENMAVFBSGINQQ-UHFFFAOYSA-N N-[bis(dibutylamino)-[8-(2-methylprop-1-enylsilyl)octyl]silyl]-N-butylbutan-1-amine Chemical compound CC(=C[SiH2]CCCCCCCC[Si](N(CCCC)CCCC)(N(CCCC)CCCC)N(CCCC)CCCC)C FENMAVFBSGINQQ-UHFFFAOYSA-N 0.000 description 1
- DWWIZHDPPTZYKW-UHFFFAOYSA-N N-[bis(diethylamino)-[2-[[ethenyl(dimethyl)silyl]oxy-dimethylsilyl]ethyl]silyl]-N-ethylethanamine Chemical compound C(=C)[Si](O[Si](CC[Si](N(CC)CC)(N(CC)CC)N(CC)CC)(C)C)(C)C DWWIZHDPPTZYKW-UHFFFAOYSA-N 0.000 description 1
- XPDXNUPQYBHWEU-UHFFFAOYSA-N N-[bis(diethylamino)-[3-(2-methylprop-1-enylsilyl)propyl]silyl]-N-ethylethanamine Chemical compound CC(=C[SiH2]CCC[Si](N(CC)CC)(N(CC)CC)N(CC)CC)C XPDXNUPQYBHWEU-UHFFFAOYSA-N 0.000 description 1
- QOJSCUWKJMAUHO-UHFFFAOYSA-N N-[bis(diethylamino)-[8-(2-methylprop-1-enylsilyl)octyl]silyl]-N-ethylethanamine Chemical compound CC(=C[SiH2]CCCCCCCC[Si](N(CC)CC)(N(CC)CC)N(CC)CC)C QOJSCUWKJMAUHO-UHFFFAOYSA-N 0.000 description 1
- DJAKHQUUBIHYCG-UHFFFAOYSA-N N-[bis(dimethylamino)-(2-methylprop-1-enylsilylmethyl)silyl]-N-methylmethanamine Chemical compound CC(=C[SiH2]C[Si](N(C)C)(N(C)C)N(C)C)C DJAKHQUUBIHYCG-UHFFFAOYSA-N 0.000 description 1
- DZUXJVVROBBOOR-UHFFFAOYSA-N N-[dimethyl-[2-(2-methylprop-1-enylsilyl)ethyl]silyl]-N-ethylethanamine Chemical compound CC(=C[SiH2]CC[Si](C)(C)N(CC)CC)C DZUXJVVROBBOOR-UHFFFAOYSA-N 0.000 description 1
- AJVDEJDJTOOWSN-UHFFFAOYSA-N N-[dimethyl-[3-(2-methylprop-1-enylsilyl)propyl]silyl]-N-ethylethanamine Chemical compound CC(=C[SiH2]CCC[Si](C)(C)N(CC)CC)C AJVDEJDJTOOWSN-UHFFFAOYSA-N 0.000 description 1
- FDDQWDZSONZNTO-UHFFFAOYSA-N N-[dimethyl-[8-(2-methylprop-1-enylsilyl)octyl]silyl]-N-ethylethanamine Chemical compound CC(=C[SiH2]CCCCCCCC[Si](C)(C)N(CC)CC)C FDDQWDZSONZNTO-UHFFFAOYSA-N 0.000 description 1
- XKCMZALRWDYOKD-UHFFFAOYSA-N N-butyl-N-[(dibutylamino)-[2-[[ethenyl(dimethyl)silyl]oxy-dimethylsilyl]ethyl]-methylsilyl]butan-1-amine Chemical compound C(=C)[Si](O[Si](CC[Si](N(CCCC)CCCC)(N(CCCC)CCCC)C)(C)C)(C)C XKCMZALRWDYOKD-UHFFFAOYSA-N 0.000 description 1
- CYLFLSBWZPOZBG-UHFFFAOYSA-N N-butyl-N-[2-[[ethenyl(dimethyl)silyl]oxy-dimethylsilyl]ethyl-dimethylsilyl]butan-1-amine Chemical compound C(=C)[Si](O[Si](CC[Si](N(CCCC)CCCC)(C)C)(C)C)(C)C CYLFLSBWZPOZBG-UHFFFAOYSA-N 0.000 description 1
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000005369 trialkoxysilyl group Chemical group 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- JYTLRNFTVQDKHP-UHFFFAOYSA-N tribromo(2-methylprop-1-enylsilylmethyl)silane Chemical compound CC(=C[SiH2]C[Si](Br)(Br)Br)C JYTLRNFTVQDKHP-UHFFFAOYSA-N 0.000 description 1
- OSZGHKRBCSLXFZ-UHFFFAOYSA-N tribromo-[2-(2-methylprop-1-enylsilyl)ethyl]silane Chemical compound CC(=C[SiH2]CC[Si](Br)(Br)Br)C OSZGHKRBCSLXFZ-UHFFFAOYSA-N 0.000 description 1
- ZBWDKHQYLBCZTF-UHFFFAOYSA-N tribromo-[3-(2-methylprop-1-enylsilyl)propyl]silane Chemical compound CC(=C[SiH2]CCC[Si](Br)(Br)Br)C ZBWDKHQYLBCZTF-UHFFFAOYSA-N 0.000 description 1
- RKZSRYWPBYJGJU-UHFFFAOYSA-N tribromo-[8-(2-methylprop-1-enylsilyl)octyl]silane Chemical compound CC(=C[SiH2]CCCCCCCC[Si](Br)(Br)Br)C RKZSRYWPBYJGJU-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- MXRHVYYCVDJLDF-UHFFFAOYSA-N trichloro(2-methylprop-1-enylsilylmethyl)silane Chemical compound CC(=C[SiH2]C[Si](Cl)(Cl)Cl)C MXRHVYYCVDJLDF-UHFFFAOYSA-N 0.000 description 1
- MIXFQWAVZKSDIR-UHFFFAOYSA-N trichloro-[2-(2-methylprop-1-enylsilyl)ethyl]silane Chemical compound CC(=C[SiH2]CC[Si](Cl)(Cl)Cl)C MIXFQWAVZKSDIR-UHFFFAOYSA-N 0.000 description 1
- PRGGAOBWBODJJV-UHFFFAOYSA-N trichloro-[2-[[ethenyl(dimethyl)silyl]oxy-dimethylsilyl]ethyl]silane Chemical compound C(=C)[Si](O[Si](CC[Si](Cl)(Cl)Cl)(C)C)(C)C PRGGAOBWBODJJV-UHFFFAOYSA-N 0.000 description 1
- KSQQZDDNHZEXTG-UHFFFAOYSA-N trichloro-[3-(2-methylprop-1-enylsilyl)propyl]silane Chemical compound CC(=C[SiH2]CCC[Si](Cl)(Cl)Cl)C KSQQZDDNHZEXTG-UHFFFAOYSA-N 0.000 description 1
- SOMZYQLROOWLNO-UHFFFAOYSA-N trichloro-[8-(2-methylprop-1-enylsilyl)octyl]silane Chemical compound CC(=C[SiH2]CCCCCCCC[Si](Cl)(Cl)Cl)C SOMZYQLROOWLNO-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- XPXGAXKUTNLCSC-UHFFFAOYSA-N triiodo(2-methylprop-1-enylsilylmethyl)silane Chemical compound CC(=C[SiH2]C[Si](I)(I)I)C XPXGAXKUTNLCSC-UHFFFAOYSA-N 0.000 description 1
- ZTKJRJAIAQACTO-UHFFFAOYSA-N triiodo-[2-(2-methylprop-1-enylsilyl)ethyl]silane Chemical compound CC(=C[SiH2]CC[Si](I)(I)I)C ZTKJRJAIAQACTO-UHFFFAOYSA-N 0.000 description 1
- TUWSMVWLHJXDIW-UHFFFAOYSA-N triiodo-[3-(2-methylprop-1-enylsilyl)propyl]silane Chemical compound CC(=C[SiH2]CCC[Si](I)(I)I)C TUWSMVWLHJXDIW-UHFFFAOYSA-N 0.000 description 1
- WTKCFRCDXXYJTQ-UHFFFAOYSA-N triiodo-[8-(2-methylprop-1-enylsilyl)octyl]silane Chemical compound CC(=C[SiH2]CCCCCCCC[Si](I)(I)I)C WTKCFRCDXXYJTQ-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- FIRONMRRDKENKJ-UHFFFAOYSA-N tris(4-methylpiperazin-1-yl)-(2-methylprop-1-enylsilylmethyl)silane Chemical compound CC(=C[SiH2]C[Si](N1CCN(CC1)C)(N1CCN(CC1)C)N1CCN(CC1)C)C FIRONMRRDKENKJ-UHFFFAOYSA-N 0.000 description 1
- PDQDSHADQYAAOY-UHFFFAOYSA-N tris(4-methylpiperazin-1-yl)-[2-(2-methylprop-1-enylsilyl)ethyl]silane Chemical compound CC(=C[SiH2]CC[Si](N1CCN(CC1)C)(N1CCN(CC1)C)N1CCN(CC1)C)C PDQDSHADQYAAOY-UHFFFAOYSA-N 0.000 description 1
- PKIBKYZWOKIVLO-UHFFFAOYSA-N tris(4-methylpiperazin-1-yl)-[8-(2-methylprop-1-enylsilyl)octyl]silane Chemical compound CC(=C[SiH2]CCCCCCCC[Si](N1CCN(CC1)C)(N1CCN(CC1)C)N1CCN(CC1)C)C PKIBKYZWOKIVLO-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/0825—Preparations of compounds not comprising Si-Si or Si-cyano linkages
- C07F7/0827—Syntheses with formation of a Si-C bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/0825—Preparations of compounds not comprising Si-Si or Si-cyano linkages
- C07F7/083—Syntheses without formation of a Si-C bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
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Description
上記官能基導入方法の一つとして、目的の官能基と不飽和結合を有する化合物を高分子改質剤として用いて、高分子化合物に当該官能基を導入する方法が知られており、例えば、ビニルトリメトキシシランを用いてポリオレフィンを変性する方法が挙げられる(特許文献1)。
その他、特許文献1記載の無水マレイン酸を用いてポリオレフィンを変性する方法(特許文献2)、ポリオレフィンをN−ビニルアルキルアミド化合物を用いて変性する方法(特許文献3)、アクリルアミド化合物を用いて熱可塑性エラストマーを変性する方法(特許文献4)などが挙げられる。
最近では高分子化合物の使用目的の多様化に伴い、更なる高分子化合物の特性向上が望まれており、変性による特性向上をより図ることができる高分子改質剤が求められている。
1. 下記一般式(1)で表される不飽和結合含有ビスシリル化合物、
2. 下記一般式(2)
で表される不飽和結合含有ハロシラン化合物と、下記一般式(3)
R8R9NH (3)
(式中、R8およびR9は、前記と同じ意味を表す。)
で表されるアミン化合物とを反応させる1の不飽和結合含有ビスシリル化合物の製造方法
を提供する。
本発明に係る不飽和結合含有ビスシリル化合物は、下記一般式(1)で示される。
上記1価炭化水素基としては、直鎖状、分岐鎖状または環状のいずれでもよく、その具体例としては、メチル、エチル、プロピル、ブチル、ペンチル、ヘキシル、ヘプチル、オクチル、デシル、ドデシル、テトラデシル、ヘキサデシル、オクタデシル、イコシル基等の直鎖状のアルキル基;イソプロピル、イソブチル、sec−ブチル、tert−ブチル、テキシル、2−エチルヘキシル基等の分岐鎖状のアルキル基;シクロペンチル、シクロヘキシル基等の環状のアルキル基;ビニル、アリル、ブテニル、ペンテニル基等のアルケニル基;フェニル、トリル基等のアリール基;ベンジル基等のアラルキル基などが挙げられる。
これらの中でも、特に原料の入手容易性や、生成物の有用性の観点から、R1〜R3としては水素原子が好ましく、R4、R5およびR7としては、メチル、エチル、プロピル基等の炭素数1〜3のアルキル基;アリル、ブテニル、ペンテニル基等の炭素数1〜5のアルケニル基が好ましい。
なお、上記ヘテロ原子は2種以上含まれていてもよく、また、アルキレン鎖末端にヘテロ原子が存在していてもよく、そのような2価の基としては、−O−Si(CH3)2−CH2−CH2−等が挙げられる。
R8およびR9の炭素数1〜20の置換または非置換の1価炭化水素基の具体例としては、上記R1〜R5およびR7で例示した基と同様のものが挙げられる。
一方、R8およびR9が互いに結合して窒素原子と共に形成する炭素数2〜20の環構造としては、アジリジン環、アゼチジン環、ピロリジン環、ピペリジン環、ピペラジン環、4−メチルピペラジン環、モルホリン環、アゼパン環等が挙げられ、中でも、原料の入手容易性や、生成物の有用性の観点から、ピロリジン環、ピペリジン環、4−メチルピペラジン環、モルホリン環が好ましい。
(式中、R8およびR9は、上記と同じ意味を表す。)
その他の含窒素化合物の具体例としては、トリメチルアミン、トリエチルアミン、トリプロピルアミン、トリブチルアミン、エチルジイソプロピルアミン、ピリジン、ジメチルアミノピリジン、ジメチルアニリン、メチルイミダゾール、テトラメチルエチレンジアミン、1,8−ジアザビシクロ[5.4.0]ウンデセン−7等が挙げられる。
その他の含窒素化合物の使用量は特に限定されないが、反応性、生産性の点から、上記一般式(2)で示される不飽和結合含有ハロシラン化合物1molに対し、0.3〜10.0mol、特に0.5〜5.0molの範囲が好ましい。
このような触媒の具体例としては、硫酸、メタンスルホン酸、ベンゼンスルホン酸、トルエンスルホン酸、ドデシルベンゼンスルホン酸、トリフルオロメタンスルホン酸等のスルホン酸化合物、塩酸、硝酸、およびこれらの酸の塩が挙げられる。
触媒の使用量は特に限定されないが、反応性、生産性の点から、上記一般式(2)で示される化合物1molに対し、0.0001〜0.1mol、特に0.001〜0.05molの範囲が好ましい。
反応雰囲気は窒素、アルゴン等の不活性ガス雰囲気とすることが好ましい。
使用可能な溶媒の具体例としては、ペンタン、ヘキサン、シクロヘキサン、ヘプタン、イソオクタン、ベンゼン、トルエン、キシレン等の炭化水素系溶媒;ジエチルエーテル、テトラヒドロフラン、ジオキサン等のエーテル系溶媒;酢酸エチル、酢酸ブチル等のエステル系溶媒;アセトニトリル、N,N−ジメチルホルムアミド、N−メチルピロリドン等の非プロトン性極性溶媒;ジクロロメタン、クロロホルム等の塩素化炭化水素系溶媒などが挙げられ、これらの溶媒は1種を単独で使用してもよく、あるいは2種以上を混合して使用してもよい。
以上のようにして塩を除去した反応液からは、蒸留、低沸点化合物留去等の通常の方法で目的物を回収することができる。
撹拌機、還流器、滴下ロートおよび温度計を備えたフラスコに、1−(ジメチルビニルシリル)−2−(ジクロロメチルシリル)エタン45.5g(0.2mol)、メタンスルホン酸0.4g(0.004mol)、トルエン120mlを仕込み、50℃に加熱した。内温が安定した後、ジエチルアミン61.4g(0.84mol)を1時間かけて滴下し、その温度で10時間撹拌した。室温まで冷却後、20質量%水酸化ナトリウム水溶液90gを加え、下層を除去した。上層である有機層を蒸留し、沸点123℃/0.4kPaの留分35.3gを得た。
質量スペクトル
m/z 300,285,228,212,187,116
撹拌機、還流器、滴下ロートおよび温度計を備えたフラスコに、1−ビニル−1,1,3,3,6−ペンタメチル−6,6−ジクロロ−2−オキサ−1,3,6−トリシラヘキサン75.4g(0.25mol)、メタンスルホン酸0.5g(0.005mol)、トルエン150mlを仕込み、50℃に加熱した。内温が安定した後、ジエチルアミン76.8g(1.05mol)を1時間かけて滴下し、その温度で8時間撹拌した。室温まで冷却後、生じた塩をろ過により除去した。ろ液を蒸留し、沸点142−143℃/0.4kPaの留分82.5gを得た。
質量スペクトル
m/z 374,302,286,231,187,116
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EP18166048.1A EP3392255B1 (en) | 2017-04-18 | 2018-04-06 | Unsaturated bond-containing bissilyl compound and making method |
KR1020180043053A KR102326216B1 (ko) | 2017-04-18 | 2018-04-13 | 불포화 결합 함유 비스실릴 화합물 및 그의 제조 방법 |
TW107113010A TWI724294B (zh) | 2017-04-18 | 2018-04-17 | 含有不飽和鍵結之雙甲矽烷基化合物及其製造方法 |
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