JP2009039613A - 触媒組成物及びそれを用いたクロスカップリング化合物の製造方法 - Google Patents
触媒組成物及びそれを用いたクロスカップリング化合物の製造方法 Download PDFInfo
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- JP2009039613A JP2009039613A JP2007205231A JP2007205231A JP2009039613A JP 2009039613 A JP2009039613 A JP 2009039613A JP 2007205231 A JP2007205231 A JP 2007205231A JP 2007205231 A JP2007205231 A JP 2007205231A JP 2009039613 A JP2009039613 A JP 2009039613A
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- 239000003054 catalyst Substances 0.000 title claims abstract description 39
- 239000000203 mixture Substances 0.000 title claims abstract description 32
- 150000001875 compounds Chemical class 0.000 title claims abstract description 31
- 238000006880 cross-coupling reaction Methods 0.000 title claims abstract description 28
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 9
- -1 amine compound Chemical class 0.000 claims abstract description 80
- 125000004185 ester group Chemical group 0.000 claims abstract description 33
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims abstract description 28
- 150000002816 nickel compounds Chemical class 0.000 claims abstract description 17
- 238000006243 chemical reaction Methods 0.000 claims abstract description 16
- 125000001072 heteroaryl group Chemical group 0.000 claims description 30
- 125000003118 aryl group Chemical group 0.000 claims description 28
- 125000003342 alkenyl group Chemical group 0.000 claims description 22
- 125000004122 cyclic group Chemical group 0.000 claims description 21
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 20
- 125000005843 halogen group Chemical group 0.000 claims description 19
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 125000003277 amino group Chemical group 0.000 claims description 10
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 10
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 8
- 229910052796 boron Inorganic materials 0.000 claims description 8
- AFVFQIVMOAPDHO-UHFFFAOYSA-M methanesulfonate group Chemical group CS(=O)(=O)[O-] AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 claims description 8
- 125000005490 tosylate group Chemical group 0.000 claims description 8
- 125000002827 triflate group Chemical group FC(S(=O)(=O)O*)(F)F 0.000 claims description 6
- 150000001491 aromatic compounds Chemical class 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- TXXWBTOATXBWDR-UHFFFAOYSA-N n,n,n',n'-tetramethylhexane-1,6-diamine Chemical compound CN(C)CCCCCCN(C)C TXXWBTOATXBWDR-UHFFFAOYSA-N 0.000 claims description 2
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims description 2
- 150000001721 carbon Chemical group 0.000 claims 4
- 239000007809 chemical reaction catalyst Substances 0.000 claims 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 26
- 238000003786 synthesis reaction Methods 0.000 abstract description 5
- 230000000694 effects Effects 0.000 abstract description 4
- 150000002366 halogen compounds Chemical class 0.000 abstract 1
- 239000002904 solvent Substances 0.000 description 16
- 229910052757 nitrogen Inorganic materials 0.000 description 15
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000002585 base Substances 0.000 description 7
- 238000006069 Suzuki reaction reaction Methods 0.000 description 5
- GEEGPFGTMRWCID-UHFFFAOYSA-N 1-n,1-n,1-n',1-n'-tetramethylbutane-1,1-diamine Chemical compound CCCC(N(C)C)N(C)C GEEGPFGTMRWCID-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- 238000005859 coupling reaction Methods 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 4
- JRTIUDXYIUKIIE-KZUMESAESA-N (1z,5z)-cycloocta-1,5-diene;nickel Chemical compound [Ni].C\1C\C=C/CC\C=C/1.C\1C\C=C/CC\C=C/1 JRTIUDXYIUKIIE-KZUMESAESA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 3
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- QULYNCCPRWKEMF-UHFFFAOYSA-N parachlorobenzotrifluoride Chemical compound FC(F)(F)C1=CC=C(Cl)C=C1 QULYNCCPRWKEMF-UHFFFAOYSA-N 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- QZKVVOXAEBCLPZ-UHFFFAOYSA-N (2-ethoxycarbonylphenyl)boronic acid Chemical compound CCOC(=O)C1=CC=CC=C1B(O)O QZKVVOXAEBCLPZ-UHFFFAOYSA-N 0.000 description 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- HVRUGFJYCAFAAN-UHFFFAOYSA-N 1-bromo-2-ethylbenzene Chemical compound CCC1=CC=CC=C1Br HVRUGFJYCAFAAN-UHFFFAOYSA-N 0.000 description 2
- URFPRAHGGBYNPW-UHFFFAOYSA-N 1-bromo-4-ethylbenzene Chemical compound CCC1=CC=C(Br)C=C1 URFPRAHGGBYNPW-UHFFFAOYSA-N 0.000 description 2
- LULAYUGMBFYYEX-UHFFFAOYSA-N 3-chlorobenzoic acid Chemical compound OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000003905 agrochemical Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 125000003828 azulenyl group Chemical group 0.000 description 2
- 150000007514 bases Chemical group 0.000 description 2
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 125000002704 decyl group Chemical group [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])* 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- GWSVBHPDADKLEQ-UHFFFAOYSA-N ethyl 2-[4-(trifluoromethyl)phenyl]benzoate Chemical compound CCOC(=O)C1=CC=CC=C1C1=CC=C(C(F)(F)F)C=C1 GWSVBHPDADKLEQ-UHFFFAOYSA-N 0.000 description 2
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 2
- 125000001041 indolyl group Chemical group 0.000 description 2
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- VOKXPKSMYJLAIW-UHFFFAOYSA-N nickel;phosphane Chemical compound P.[Ni] VOKXPKSMYJLAIW-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 125000005581 pyrene group Chemical group 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 description 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 2
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LKWVHTKYVYPVBE-UHFFFAOYSA-N (2-acetyloxyphenyl)boronic acid Chemical compound CC(=O)OC1=CC=CC=C1B(O)O LKWVHTKYVYPVBE-UHFFFAOYSA-N 0.000 description 1
- BEHBHYYPTOHUHX-UHFFFAOYSA-N (2-bromophenyl) acetate Chemical compound CC(=O)OC1=CC=CC=C1Br BEHBHYYPTOHUHX-UHFFFAOYSA-N 0.000 description 1
- CJPVPOYTTALCNX-UHFFFAOYSA-N (2-chlorophenyl) acetate Chemical compound CC(=O)OC1=CC=CC=C1Cl CJPVPOYTTALCNX-UHFFFAOYSA-N 0.000 description 1
- SNIVHZRVLQLTLY-UHFFFAOYSA-N (2-iodophenyl) acetate Chemical compound CC(=O)OC1=CC=CC=C1I SNIVHZRVLQLTLY-UHFFFAOYSA-N 0.000 description 1
- ODAXNYMENLFYMY-UHFFFAOYSA-N (2-methoxycarbonylphenyl)boronic acid Chemical compound COC(=O)C1=CC=CC=C1B(O)O ODAXNYMENLFYMY-UHFFFAOYSA-N 0.000 description 1
- UPJNXMMBLATBOH-UHFFFAOYSA-N (2-phenylmethoxycarbonylphenyl)boronic acid Chemical compound OB(O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 UPJNXMMBLATBOH-UHFFFAOYSA-N 0.000 description 1
- CDLTWXBTYNNYLN-UHFFFAOYSA-N (3-bromophenyl) acetate Chemical compound CC(=O)OC1=CC=CC(Br)=C1 CDLTWXBTYNNYLN-UHFFFAOYSA-N 0.000 description 1
- GQTKYLQYHPTULY-UHFFFAOYSA-N (3-chlorophenyl) acetate Chemical compound CC(=O)OC1=CC=CC(Cl)=C1 GQTKYLQYHPTULY-UHFFFAOYSA-N 0.000 description 1
- LWGMUQGQHHKINA-UHFFFAOYSA-N (3-iodophenyl) acetate Chemical compound CC(=O)OC1=CC=CC(I)=C1 LWGMUQGQHHKINA-UHFFFAOYSA-N 0.000 description 1
- XEXHCQJRVMVJMY-UHFFFAOYSA-N (4-bromophenyl) acetate Chemical compound CC(=O)OC1=CC=C(Br)C=C1 XEXHCQJRVMVJMY-UHFFFAOYSA-N 0.000 description 1
- KEUPLGRNURQXAR-UHFFFAOYSA-N (4-chlorophenyl) acetate Chemical compound CC(=O)OC1=CC=C(Cl)C=C1 KEUPLGRNURQXAR-UHFFFAOYSA-N 0.000 description 1
- MXHYFISNECFQHA-UHFFFAOYSA-N (4-iodophenyl) acetate Chemical compound CC(=O)OC1=CC=C(I)C=C1 MXHYFISNECFQHA-UHFFFAOYSA-N 0.000 description 1
- FBECTVVCBRAZRM-MDZDMXLPSA-N (E)-1-chlorodec-1-ene Chemical compound CCCCCCCC\C=C\Cl FBECTVVCBRAZRM-MDZDMXLPSA-N 0.000 description 1
- SYSZENVIJHPFNL-UHFFFAOYSA-N (alpha-D-mannosyl)7-beta-D-mannosyl-diacetylchitobiosyl-L-asparagine, isoform B (protein) Chemical compound COC1=CC=C(I)C=C1 SYSZENVIJHPFNL-UHFFFAOYSA-N 0.000 description 1
- IUXHPSPHPKXTPA-ONEGZZNKSA-N (e)-1-bromobut-1-ene Chemical compound CC\C=C\Br IUXHPSPHPKXTPA-ONEGZZNKSA-N 0.000 description 1
- PWJJHLRABLZGCK-MDZDMXLPSA-N (e)-1-bromodec-1-ene Chemical compound CCCCCCCC\C=C\Br PWJJHLRABLZGCK-MDZDMXLPSA-N 0.000 description 1
- XNCAEAZUROUZKT-VOTSOKGWSA-N (e)-1-bromohept-1-ene Chemical compound CCCCC\C=C\Br XNCAEAZUROUZKT-VOTSOKGWSA-N 0.000 description 1
- FBUZNPORDKVYFD-AATRIKPKSA-N (e)-1-bromohex-1-ene Chemical compound CCCC\C=C\Br FBUZNPORDKVYFD-AATRIKPKSA-N 0.000 description 1
- WSXIDSNEEOYBFA-SNAWJCMRSA-N (e)-1-bromopent-1-ene Chemical compound CCC\C=C\Br WSXIDSNEEOYBFA-SNAWJCMRSA-N 0.000 description 1
- DUDKKPVINWLFBI-ONEGZZNKSA-N (e)-1-chlorobut-1-ene Chemical compound CC\C=C\Cl DUDKKPVINWLFBI-ONEGZZNKSA-N 0.000 description 1
- CLFJXJXGJWCBSU-VOTSOKGWSA-N (e)-1-chlorohept-1-ene Chemical compound CCCCC\C=C\Cl CLFJXJXGJWCBSU-VOTSOKGWSA-N 0.000 description 1
- NKNYZKFBNQUWTM-SNAWJCMRSA-N (e)-1-chloropent-1-ene Chemical compound CCC\C=C\Cl NKNYZKFBNQUWTM-SNAWJCMRSA-N 0.000 description 1
- XULQQNDHGTXWAD-VOTSOKGWSA-N (e)-1-iodohept-1-ene Chemical compound CCCCC\C=C\I XULQQNDHGTXWAD-VOTSOKGWSA-N 0.000 description 1
- TUAPXMNNQGXDDV-AATRIKPKSA-N (e)-1-iodohex-1-ene Chemical compound CCCC\C=C\I TUAPXMNNQGXDDV-AATRIKPKSA-N 0.000 description 1
- SJZDDNSUIVLYIN-BQYQJAHWSA-N (e)-1-iodooct-1-ene Chemical compound CCCCCC\C=C\I SJZDDNSUIVLYIN-BQYQJAHWSA-N 0.000 description 1
- WQONPSCCEXUXTQ-UHFFFAOYSA-N 1,2-dibromobenzene Chemical compound BrC1=CC=CC=C1Br WQONPSCCEXUXTQ-UHFFFAOYSA-N 0.000 description 1
- ZPQOPVIELGIULI-UHFFFAOYSA-N 1,3-dichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1 ZPQOPVIELGIULI-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- SWJPEBQEEAHIGZ-UHFFFAOYSA-N 1,4-dibromobenzene Chemical compound BrC1=CC=C(Br)C=C1 SWJPEBQEEAHIGZ-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical group C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 1
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 1
- BSIMCZKQHTVQBG-UHFFFAOYSA-N 1-(1-ethoxyethoxy)-2-iodobenzene Chemical compound CCOC(C)OC1=CC=CC=C1I BSIMCZKQHTVQBG-UHFFFAOYSA-N 0.000 description 1
- WSHAUVRKJZSMOA-UHFFFAOYSA-N 1-(1-ethoxyethoxy)-3-iodobenzene Chemical compound CCOC(C)OC1=CC=CC(I)=C1 WSHAUVRKJZSMOA-UHFFFAOYSA-N 0.000 description 1
- LWKXEKLPISSDFY-UHFFFAOYSA-N 1-(1-ethoxyethoxy)-4-iodobenzene Chemical compound CCOC(C)OC1=CC=C(I)C=C1 LWKXEKLPISSDFY-UHFFFAOYSA-N 0.000 description 1
- ZDOYHCIRUPHUHN-UHFFFAOYSA-N 1-(2-chlorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC=C1Cl ZDOYHCIRUPHUHN-UHFFFAOYSA-N 0.000 description 1
- XDXCBCXNCQGZPG-UHFFFAOYSA-N 1-(2-iodophenyl)ethanone Chemical compound CC(=O)C1=CC=CC=C1I XDXCBCXNCQGZPG-UHFFFAOYSA-N 0.000 description 1
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- UUWJBXKHMMQDED-UHFFFAOYSA-N 1-(3-chlorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(Cl)=C1 UUWJBXKHMMQDED-UHFFFAOYSA-N 0.000 description 1
- IWLHOUBDKCKJJQ-UHFFFAOYSA-N 1-(3-iodophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(I)=C1 IWLHOUBDKCKJJQ-UHFFFAOYSA-N 0.000 description 1
- WYECURVXVYPVAT-UHFFFAOYSA-N 1-(4-bromophenyl)ethanone Chemical compound CC(=O)C1=CC=C(Br)C=C1 WYECURVXVYPVAT-UHFFFAOYSA-N 0.000 description 1
- BUZYGTVTZYSBCU-UHFFFAOYSA-N 1-(4-chlorophenyl)ethanone Chemical compound CC(=O)C1=CC=C(Cl)C=C1 BUZYGTVTZYSBCU-UHFFFAOYSA-N 0.000 description 1
- JZJWCDQGIPQBAO-UHFFFAOYSA-N 1-(4-iodophenyl)ethanone Chemical compound CC(=O)C1=CC=C(I)C=C1 JZJWCDQGIPQBAO-UHFFFAOYSA-N 0.000 description 1
- ZXNZSVMDZXRCJW-UHFFFAOYSA-N 1-N,1-N,1-N',1-N'-tetraethyldodecane-1,1-diamine Chemical compound C(C)N(CC)C(CCCCCCCCCCC)N(CC)CC ZXNZSVMDZXRCJW-UHFFFAOYSA-N 0.000 description 1
- XTKLFCLOKULKOU-UHFFFAOYSA-N 1-N,1-N,1-N',1-N'-tetraethylnonane-1,1-diamine Chemical compound CCCCCCCCC(N(CC)CC)N(CC)CC XTKLFCLOKULKOU-UHFFFAOYSA-N 0.000 description 1
- LJDNTGATLKJQNN-UHFFFAOYSA-N 1-N,1-N,1-N',1-N'-tetraethyloctane-1,1-diamine Chemical compound CCCCCCCC(N(CC)CC)N(CC)CC LJDNTGATLKJQNN-UHFFFAOYSA-N 0.000 description 1
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical group C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 1
- AEEVVWXVCMROBH-UHFFFAOYSA-N 1-bromo-2-(1-ethoxyethoxy)benzene Chemical compound CCOC(C)OC1=CC=CC=C1Br AEEVVWXVCMROBH-UHFFFAOYSA-N 0.000 description 1
- RWXUNIMBRXGNEP-UHFFFAOYSA-N 1-bromo-2-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1Br RWXUNIMBRXGNEP-UHFFFAOYSA-N 0.000 description 1
- JBSSNSQYEIJWJT-UHFFFAOYSA-N 1-bromo-2-[(2-methylpropan-2-yl)oxy]benzene Chemical compound CC(C)(C)OC1=CC=CC=C1Br JBSSNSQYEIJWJT-UHFFFAOYSA-N 0.000 description 1
- UEVKWTASYVIROP-UHFFFAOYSA-N 1-bromo-2-butylbenzene Chemical compound CCCCC1=CC=CC=C1Br UEVKWTASYVIROP-UHFFFAOYSA-N 0.000 description 1
- QBELEDRHMPMKHP-UHFFFAOYSA-N 1-bromo-2-chlorobenzene Chemical compound ClC1=CC=CC=C1Br QBELEDRHMPMKHP-UHFFFAOYSA-N 0.000 description 1
- JVEQWIQHHWNMQX-UHFFFAOYSA-N 1-bromo-2-ethoxybenzene Chemical compound CCOC1=CC=CC=C1Br JVEQWIQHHWNMQX-UHFFFAOYSA-N 0.000 description 1
- IPWBFGUBXWMIPR-UHFFFAOYSA-N 1-bromo-2-fluorobenzene Chemical compound FC1=CC=CC=C1Br IPWBFGUBXWMIPR-UHFFFAOYSA-N 0.000 description 1
- HTDQSWDEWGSAMN-UHFFFAOYSA-N 1-bromo-2-methoxybenzene Chemical compound COC1=CC=CC=C1Br HTDQSWDEWGSAMN-UHFFFAOYSA-N 0.000 description 1
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- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- GRJHONXDTNBDTC-UHFFFAOYSA-N phenyl trifluoromethanesulfonate Chemical compound FC(F)(F)S(=O)(=O)OC1=CC=CC=C1 GRJHONXDTNBDTC-UHFFFAOYSA-N 0.000 description 1
- NIXKBAZVOQAHGC-UHFFFAOYSA-M phenylmethanesulfonate Chemical compound [O-]S(=O)(=O)CC1=CC=CC=C1 NIXKBAZVOQAHGC-UHFFFAOYSA-M 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000005412 pyrazyl group Chemical group 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000005063 tetradecenyl group Chemical group C(=CCCCCCCCCCCCC)* 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000005040 tridecenyl group Chemical group C(=CCCCCCCCCCCC)* 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
- TWQULNDIKKJZPH-UHFFFAOYSA-K trilithium;phosphate Chemical compound [Li+].[Li+].[Li+].[O-]P([O-])([O-])=O TWQULNDIKKJZPH-UHFFFAOYSA-K 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
- 235000019798 tripotassium phosphate Nutrition 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 125000005065 undecenyl group Chemical group C(=CCCCCCCCCC)* 0.000 description 1
- 125000002948 undecyl 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])[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
【解決手段】 0価のニッケル化合物、特定のアミン化合物及びトリフェニルホスフィンを含んでなる触媒組成物を用いて、塩基の存在下に、オルト位に少なくとも1つのエステル基を有する芳香族ホウ素化合物とハロゲン化合物等とを反応させることによりクロスカップリング化合物を得る。
【選択図】 なし
Description
以下、本発明について詳細に説明する。
上記したニッケル化合物は単独または混合物として使用してもよい。なお、反応性及び収率の観点からは、ビス(1,5−シクロオクタジエン)ニッケルを用いることが好ましい。
一般式(2)で示される第三級の二座アミン化合物の具体例としては、例えば、N,N,N’,N’−テトラメチルブタンジアミン、N,N,N’,N’−テトラエチルブタンジアミン、N,N,N’,N’−テトラシクロヘキシルブタンジアミン、N,N,N’,N’−テトラフェニルブタンジアミン、N,N,N’,N’−テトラメチルペンタンジアミン、N,N,N’,N’−テトラエチルペンタンジアミン、N,N,N’,N’−テトラシクロヘキシルペンタンジアミン、N,N,N’,N’−テトラフェニルペンタンジアミン、N,N,N’,N’−テトラメチルヘキサンジアミン、N,N,N’,N’−テトラエチルヘキサンジアミン、N,N,N’,N’−テトラシクロヘキシルヘキサンジアミン、N,N,N’,N’−テトラフェニルペンタヘキサンジアミン、N,N,N’,N’−テトラメチルヘプタンジアミン、N,N,N’,N’−テトラエチルヘプタンジアミン、N,N,N’,N’−テトラシクロヘキシルヘプタンジアミン、N,N,N’,N’−テトラフェニルヘプタンジアミン、N,N,N’,N’−テトラメチルオクタンジアミン、N,N,N’,N’−テトラエチルオクタンジアミン、N,N,N’,N’−テトラシクロヘキシルオクタンジアミン、N,N,N’,N’−テトラフェニルオクタンジアミン、N,N,N’,N’−テトラメチルノナンジアミン、N,N,N’,N’−テトラエチルノナンジアミン、N,N,N’,N’−テトラシクロヘキシルノナンジアミン、N,N,N’,N’−テトラフェニルノナンジアミン、N,N,N’,N’−テトラメチルデカンジアミン、N,N,N’,N’−テトラエチルデカンジアミン、N,N,N’,N’−テトラシクロヘキシルデカンジアミン、N,N,N’,N’−テトラフェニルデカンジアミン、N,N,N’,N’−テトラメチルドデカンジアミン、N,N,N’,N’−テトラエチルドデカンジアミン、N,N,N’,N’−テトラシクロヘキシルドデカンジアミン、N,N,N’,N’−テトラフェニルドデカンジアミン等が挙げられる。収率の観点からはnが6〜8の第三級の二座アミン化合物を用いることが望ましく、また、化合物入手の観点からはnが6のN,N,N’,N’−テトラメチルヘキサンジアミンを用いることが好ましい。
本発明の方法において使用されるオルト位に少なくとも1つのエステル基を有する芳香族ホウ素化合物は、上記式(3)で示される化合物である。式中、R5はホウ素原子が結合する炭素原子のオルト位に少なくとも1つのエステル基を有する、置換もしくは無置換のアリール基、置換もしくは無置換のヘテロアリール基を表す。
芳香族ホウ素化合物のより好ましい例は、下記式(6)で示されるオルト位に少なくとも1つのエステル基を有する化合物である。
上記式(6)で示されるオルト位に少なくとも1つのエステル基を有する芳香族ホウ素化合物の具体例としては特に限定されないが、例えば、2−アセトキシフェニルボロン酸、2−メトキシカルボニルフェニルボロン酸、2,4−ビス(メトキシカルボニル)フェニルボロン酸、2−エトキシカルボニルフェニルボロン酸、2,4−ビス(エトキシカルボニル)フェニルボロン酸、2−ベンジルオキシカルボニルフェニルボロン酸等が挙げられる。
上記式(7)で示される芳香族化合物の具体例としては特に限定されないが、例えば、フッ化ベンゼン、塩化ベンゼン、臭化ベンゼン、ヨウ化ベンゼン、フェニルメタンスルホナート、フェニルトリフルオロメタンスルホナート、o−クロロトルエン、m−クロロトルエン、p−クロロトルエン、o−ブロモトルエン、m−ブロモトルエン、p−ブロモトルエン、o−ヨードトルエン、m−ヨードトルエン、p−ヨードトルエン、2−エチルクロロベンゼン、3−エチルクロロベンゼン、4−エチルクロロベンゼン、2−エチルブロモベンゼン、3−エチルブロモベンゼン、4−エチルブロモベンゼン、2−エチルヨードベンゼン、3−エチルヨードベンゼン、4−エチルヨードベンゼン、2−プロピルクロロベンゼン、3−プロピルクロロベンゼン、4−プロピルクロロベンゼン、2−プロピルブロモベンゼン、3−プロピルブロモベンゼン、4−プロピルブロモベンゼン、2−プロピルヨードベンゼン、3−プロピルヨードベンゼン、4−プロピルヨードベンゼン、2−ブチルクロロベンゼン、3−ブチルクロロベンゼン、4−ブチルクロロベンゼン、2−ブチルブロモベンゼン、3−ブチルブロモベンゼン、4−ブチルブロモベンゼン、2−ブチルヨードベンゼン、3−ブチルヨードベンゼン、4−ブチルヨードベンゼン、1−クロロナフタレン、2−クロロナフタレン、1−ブロモナフタレン、2−ブロモナフタレン、1−ヨードナフタレン、2−ヨードナフタレン、o−ジクロロベンゼン、m−ジクロロベンゼン、p−ジクロロベンゼン、o−ジブロモベンゼン、m−ジブロモベンゼン、p−ジブロモベンゼン、o−ブロモクロロベンゼン、m−ブロモクロロベンゼン、p−ブロモクロロベンゼン、o−クロロフルオロベンゼン、m−クロロフルオロベンゼン、p−クロロフルオロベンゼン、o−ブロモフルオロベンゼン、m−ブロモフルオロベンゼン、p−ブロモフルオロベンゼン、o−クロロアニソール、m−クロロアニソール、p−クロロアニソール、o−ブロモアニソール、m−ブロモアニソール、p−ブロモアニソール、o−ヨードアニソール、m−ヨードアニソール、p−ヨードアニソール、o−クロロフェネトール、m−クロロフェネトール、p−クロロフェネトール、o−ブロモフェネトール、m−ブロモフェネトール、p−ブロモフェネトール、o−ヨードフェネトール、m−ヨードフェネトール、p−ヨードフェネトール、o−n−ブトキシクロロベンゼン、m−n−ブトキシクロロベンゼン、p−n−ブトキシクロロベンゼン、o−n−ブトキシブロモベンゼン、m−n−ブトキシブロモベンゼン、p−n−ブトキシブロモベンゼン、o−n−ブトキシヨードベンゼン、m−n−ブトキシヨードベンゼン、p−n−ブトキシヨードベンゼン、o−t−ブトキシクロロベンゼン、m−t−ブトキシクロロベンゼン、p−t−ブトキシクロロベンゼン、o−t−ブトキシフェニルブロマイド、m−t−ブトキシフェニルブロマイド、p−t−ブトキシフェニルブロマイド、o−t−ブトキシヨードベンゼン、m−t−ブトキシヨードベンゼン、p−t−ブトキシヨードベンゼン、2−クロロベンゾニトリル、3−クロロベンゾニトリル、4−クロロベンゾニトリル、2−ブロモベンゾニトリル、3−ブロモベンゾニトリル、4−ブロモベンゾニトリル、2−ヨードベンゾニトリル、3−ヨードベンゾニトリル、4−ヨードベンゾニトリル、o−(1−エトキシエトキシ)クロロベンゼン、m−(1−エトキシエトキシ)クロロベンゼン、p−(1−エトキシエトキシ)クロロベンゼン、o−(1−エトキシエトキシ)ブロモベンゼン、m−(1−エトキシエトキシ)ブロモベンゼン、p−(1−エトキシエトキシ)ブロモベンゼン、o−(1−エトキシエトキシ)ヨードベンゼン、m−(1−エトキシエトキシ)ヨードベンゼン、p−(1−エトキシエトキシ)ヨードベンゼン、o−アセチルクロロベンゼン、m−アセチルクロロベンゼン、p−アセチルクロロベンゼン、o−アセチルブロモベンゼン、m−アセチルブロモベンゼン、p−アセチルブロモベンゼン、o−アセチルヨードベンゼン、m−アセチルヨードベンゼン、p−アセチルヨードベンゼン、o−アセトキシクロロベンゼン、m−アセトキシクロロベンゼン、p−アセトキシクロロベンゼン、o−アセトキシブロモベンゼン、m−アセトキシブロモベンゼン、p−アセトキシブロモベンゼン、o−アセトキシヨードベンゼン、m−アセトキシヨードベンゼン、p−アセトキシヨードベンゼン、2−トリフルオロメチルクロロベンゼン、3−トリフルオロメチルクロロベンゼン、4−トリフルオロメチルクロロベンゼン、2−トリフルオロメチルブロモベンゼン、3−トリフルオロメチルブロモベンゼン、4−トリフルオロメチルブロモベンゼン、2−トリフルオロメチルヨードベンゼン、3−トリフルオロメチルヨードベンゼン、4−トリフルオロメチルヨードベンゼン、2−クロロ安息香酸、3−クロロ安息香酸、4−クロロ安息香酸、2−ブロモ安息香酸、3−ブロモ安息香酸、4−ブロモ安息香酸、2−ヨード安息香酸、3−ヨード安息香酸、4−ヨード安息香酸、2−クロロ安息香酸メチル、3−クロロ安息香酸メチル、4−クロロ安息香酸メチル、2−ブロモ安息香酸メチル、3−ブロモ安息香酸メチル、4−ブロモ安息香酸メチル、2−ヨード安息香酸メチル、3−ヨード安息香酸メチル、4−ヨード安息香酸メチル、2−クロロアニリン、3−クロロアニリン、4−クロロアニリン、2−ブロモアニリン、3−ブロモアニリン、4−ブロモアニリン、2−ヨードアニリン、3−ヨードアニリン、4−ヨードアニリン、2−クロロホルミルベンゼン、3−クロロホルミルベンゼン、4−クロロホルミルベンゼン、2−ブロモホルミルベンゼン、3−ブロモホルミルベンゼン、4−ブロモホルミルベンゼン等が挙げられる。
窒素ガスで置換された30ml反応管に、p−トリフルオロメチルクロロベンゼン 0.54g(3.0mmol)、2−エトキシカルボニルフェニルボロン酸 0.70g(3.6mmol)、ビス(1,5−シクロオクタジエン)ニッケル(Ni(cod)2) 41mg(0.15mmol)、N,N,N’,N’−テトラメチルブタンジアミン 24.5mg(0.17mmol)、トリフェニルホスフィン(PPh3) 120mg(0.45mmol)、1,4−ジオキサン 5.0g、無水リン酸三カリウム(K3PO4) 1.91g(9.0mmol)を加えて、溶媒還流温度にて12時間攪拌した。反応終了後、5%HCl水溶液を加えて後処理し、分液操作にて得られた有機層をさらに飽和NaCl水溶液で洗浄した。得られた有機層をn−ドデカンを内部標準物質とするガスクロマトグラフィー定量分析にて分析した結果、目的物である4’−トリフルオロメチル−2−ビフェニルカルボン酸エチルが、収率59%(p−トリフルオロメチルクロロベンゼン基準)の割合で生成していた。結果を表1に示す。
実施例1において、N,N,N’,N’−テトラメチルブタンジアミン 24.5mg(0.17mmol)の代わりに、表1に示したアミン化合物を用いた以外は、実施例1に準拠して反応を行った。結果を表1に示す。
実施例1において、ビス(1,5−シクロオクタジエン)ニッケル(Ni(cod)2) 41mg(0.15mmol)、N,N,N’,N’−テトラメチルブタンジアミン 24.5mg(0.17mmol)の代わりに、N,N,N’,N’−テトラメチルエチレンジアミンジクロロニッケル錯体(NiCl2(tmeda))を使用した以外は、実施例1に準拠して反応を行った。結果を表1に示す。
Claims (6)
- 0価のニッケル化合物、下記式(2)で示されるアミン化合物及びトリフェニルホスフィンを含んでなるクロスカップリング反応用触媒組成物において、下記式(3)で示されるオルト位に少なくとも1つのエステル基を有する芳香族ホウ素化合物と下記式(4)で示される化合物との反応に用いることを特徴とするクロスカップリング反応用触媒組成物。
- アミン化合物のメチレン単位を表すnが6〜8であることを特徴とする請求項1〜2に記載のクロスカップリング反応用触媒組成物。
- アミン化合物が、N,N,N’,N’−テトラメチルヘキサンジアミンであることを特徴とする請求項1に記載のクロスカップリング反応用触媒組成物。
- 下記式(3)で示されるオルト位に少なくとも1つのエステル基を有する芳香族ホウ素化合物と下記式(4)で示される化合物とを、塩基及び請求項1〜3のいずれか一項に記載の触媒組成物の存在下に、クロスカップリング反応させることを特徴とする下記式(5)で示されるクロスカップリング化合物の製造方法。
- 式(3)で示されるオルト位に少なくとも1つのエステル基を有する芳香族ホウ素化合物が、下記式(6)で示される化合物であることを特徴とする請求項4に記載のクロスカップリング化合物の製造方法。
- 式(4)で示される化合物が、下記式(7)で示される芳香族化合物、もしくは下記式(8)で示されるアルケニル化合物であることを特徴とする請求項4〜5に記載のクロスカップリング化合物の製造方法。
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