JP4162615B2 - ４，４’’’−ジヒドロキシ−ｐ−クォ―ターフェニル類の製造方法。 - Google Patents
４，４’’’−ジヒドロキシ−ｐ−クォ―ターフェニル類の製造方法。 Download PDFInfo
- Publication number
- JP4162615B2 JP4162615B2 JP2004064056A JP2004064056A JP4162615B2 JP 4162615 B2 JP4162615 B2 JP 4162615B2 JP 2004064056 A JP2004064056 A JP 2004064056A JP 2004064056 A JP2004064056 A JP 2004064056A JP 4162615 B2 JP4162615 B2 JP 4162615B2
- Authority
- JP
- Japan
- Prior art keywords
- general formula
- dihydroxy
- hydroxyphenyl
- bicyclohexene
- reaction
- 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 - Fee Related
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 239000003054 catalyst Substances 0.000 claims description 36
- 239000002904 solvent Substances 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 150000005846 sugar alcohols Polymers 0.000 claims description 3
- DQMHOURLYZPBCN-UHFFFAOYSA-N 4-[2-(4-hydroxycyclohexen-1-yl)cyclohexen-1-yl]phenol Chemical compound OC1=CC=C(C=C1)C1=C(CCCC1)C1=CCC(CC1)O DQMHOURLYZPBCN-UHFFFAOYSA-N 0.000 claims description 2
- 150000001934 cyclohexanes Chemical class 0.000 claims 1
- 150000001911 terphenyls Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 38
- -1 etc. Substances 0.000 description 33
- 238000006356 dehydrogenation reaction Methods 0.000 description 20
- 238000004458 analytical method Methods 0.000 description 16
- 239000002994 raw material Substances 0.000 description 16
- NDJYHEREZVSKQN-UHFFFAOYSA-N 4-[1-(4,4-dihydroxycyclohexyl)cyclohexyl]cyclohexa-2,4-diene-1,1-diol Chemical group OC1(CC=C(C=C1)C1(CCCCC1)C1CCC(CC1)(O)O)O NDJYHEREZVSKQN-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 238000005979 thermal decomposition reaction Methods 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 14
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 13
- 239000011541 reaction mixture Substances 0.000 description 13
- 239000000047 product Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 229920001223 polyethylene glycol Polymers 0.000 description 11
- 238000004128 high performance liquid chromatography Methods 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000001914 filtration Methods 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 239000003513 alkali Substances 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000002002 slurry Substances 0.000 description 7
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000013078 crystal Substances 0.000 description 6
- 238000004455 differential thermal analysis Methods 0.000 description 6
- 238000004949 mass spectrometry Methods 0.000 description 6
- 229910052763 palladium Inorganic materials 0.000 description 6
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 4
- 229910017052 cobalt Inorganic materials 0.000 description 4
- 239000010941 cobalt Substances 0.000 description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- ZULOKAVWRNAZOO-UHFFFAOYSA-N 4-[4-[4,4-bis(4-hydroxy-3,5-dimethylphenyl)cyclohexyl]-1-(4-hydroxy-3,5-dimethylphenyl)cyclohexyl]-2,6-dimethylphenol Chemical compound CC1=C(O)C(C)=CC(C2(CCC(CC2)C2CCC(CC2)(C=2C=C(C)C(O)=C(C)C=2)C=2C=C(C)C(O)=C(C)C=2)C=2C=C(C)C(O)=C(C)C=2)=C1 ZULOKAVWRNAZOO-UHFFFAOYSA-N 0.000 description 3
- XNWPNSZLCWLHBT-UHFFFAOYSA-N 4-[4-[4,4-bis(4-hydroxy-3-methylphenyl)cyclohexyl]-1-(4-hydroxy-3-methylphenyl)cyclohexyl]-2-methylphenol Chemical compound C1=C(O)C(C)=CC(C2(CCC(CC2)C2CCC(CC2)(C=2C=C(C)C(O)=CC=2)C=2C=C(C)C(O)=CC=2)C=2C=C(C)C(O)=CC=2)=C1 XNWPNSZLCWLHBT-UHFFFAOYSA-N 0.000 description 3
- CTTHICAWOGBDFM-UHFFFAOYSA-N 4-[4-[4,4-bis(4-hydroxy-3-propan-2-ylphenyl)cyclohexyl]-1-(4-hydroxy-3-propan-2-ylphenyl)cyclohexyl]-2-propan-2-ylphenol Chemical compound C1=C(O)C(C(C)C)=CC(C2(CCC(CC2)C2CCC(CC2)(C=2C=C(C(O)=CC=2)C(C)C)C=2C=C(C(O)=CC=2)C(C)C)C=2C=C(C(O)=CC=2)C(C)C)=C1 CTTHICAWOGBDFM-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 3
- QFLWZFQWSBQYPS-AWRAUJHKSA-N (3S)-3-[[(2S)-2-[[(2S)-2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-[1-bis(4-chlorophenoxy)phosphorylbutylamino]-4-oxobutanoic acid Chemical compound CCCC(NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12)C(C)C)P(=O)(Oc1ccc(Cl)cc1)Oc1ccc(Cl)cc1 QFLWZFQWSBQYPS-AWRAUJHKSA-N 0.000 description 2
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- QVHMSMOUDQXMRS-UHFFFAOYSA-N PPG n4 Chemical class CC(O)COC(C)COC(C)COC(C)CO QVHMSMOUDQXMRS-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-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
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 229940125773 compound 10 Drugs 0.000 description 2
- 229940125782 compound 2 Drugs 0.000 description 2
- 229940126214 compound 3 Drugs 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical compound C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- JLFNLZLINWHATN-UHFFFAOYSA-N pentaethylene glycol Chemical compound OCCOCCOCCOCCOCCO JLFNLZLINWHATN-UHFFFAOYSA-N 0.000 description 2
- 235000011181 potassium carbonates Nutrition 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- MGAXYKDBRBNWKT-UHFFFAOYSA-N (5-oxooxolan-2-yl)methyl 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)OCC1OC(=O)CC1 MGAXYKDBRBNWKT-UHFFFAOYSA-N 0.000 description 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
- OQIDYCVWAFZRTR-UHFFFAOYSA-N 4-(4-oxocyclohexyl)cyclohexan-1-one Chemical compound C1CC(=O)CCC1C1CCC(=O)CC1 OQIDYCVWAFZRTR-UHFFFAOYSA-N 0.000 description 1
- QZZFXLNHQRTWPY-UHFFFAOYSA-N 4-[4-[4,4-bis(4-hydroxy-2,3,5-trimethylphenyl)cyclohexyl]-1-(4-hydroxy-2,3,5-trimethylphenyl)cyclohexyl]-2,3,6-trimethylphenol Chemical compound CC1=C(O)C(C)=CC(C2(CCC(CC2)C2CCC(CC2)(C=2C(=C(C)C(O)=C(C)C=2)C)C=2C(=C(C)C(O)=C(C)C=2)C)C=2C(=C(C)C(O)=C(C)C=2)C)=C1C QZZFXLNHQRTWPY-UHFFFAOYSA-N 0.000 description 1
- JWBMCESOJREHAA-UHFFFAOYSA-N 4-[4-[4,4-bis(4-hydroxy-2,3,6-trimethylphenyl)cyclohexyl]-1-(4-hydroxy-2,3,6-trimethylphenyl)cyclohexyl]-2,3,5-trimethylphenol Chemical compound CC1=CC(O)=C(C)C(C)=C1C1(C=2C(=C(C)C(O)=CC=2C)C)CCC(C2CCC(CC2)(C=2C(=C(C)C(O)=CC=2C)C)C=2C(=C(C)C(O)=CC=2C)C)CC1 JWBMCESOJREHAA-UHFFFAOYSA-N 0.000 description 1
- OFBSMXAMCFSVSJ-UHFFFAOYSA-N 4-[4-[4,4-bis(4-hydroxy-2,5-dimethylphenyl)cyclohexyl]-1-(4-hydroxy-2,5-dimethylphenyl)cyclohexyl]-2,5-dimethylphenol Chemical compound C1=C(O)C(C)=CC(C2(CCC(CC2)C2CCC(CC2)(C=2C(=CC(O)=C(C)C=2)C)C=2C(=CC(O)=C(C)C=2)C)C=2C(=CC(O)=C(C)C=2)C)=C1C OFBSMXAMCFSVSJ-UHFFFAOYSA-N 0.000 description 1
- UBRCLLJDFNIILT-UHFFFAOYSA-N 4-[4-[4,4-bis(4-hydroxy-2-methylphenyl)cyclohexyl]-1-(4-hydroxy-2-methylphenyl)cyclohexyl]-3-methylphenol Chemical compound CC1=CC(O)=CC=C1C1(C=2C(=CC(O)=CC=2)C)CCC(C2CCC(CC2)(C=2C(=CC(O)=CC=2)C)C=2C(=CC(O)=CC=2)C)CC1 UBRCLLJDFNIILT-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical class OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- GXDVEXJTVGRLNW-UHFFFAOYSA-N [Cr].[Cu] Chemical compound [Cr].[Cu] GXDVEXJTVGRLNW-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- HBEQXAKJSGXAIQ-UHFFFAOYSA-N oxopalladium Chemical compound [Pd]=O HBEQXAKJSGXAIQ-UHFFFAOYSA-N 0.000 description 1
- 229910003445 palladium oxide Inorganic materials 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- ZGJADVGJIVEEGF-UHFFFAOYSA-M potassium;phenoxide Chemical compound [K+].[O-]C1=CC=CC=C1 ZGJADVGJIVEEGF-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004064056A JP4162615B2 (ja) | 2004-03-08 | 2004-03-08 | ４，４’’’−ジヒドロキシ−ｐ−クォ―ターフェニル類の製造方法。 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004064056A JP4162615B2 (ja) | 2004-03-08 | 2004-03-08 | ４，４’’’−ジヒドロキシ−ｐ−クォ―ターフェニル類の製造方法。 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008148964A Division JP4829927B2 (ja) | 2008-06-06 | 2008-06-06 | ４，４’’’−ジヒドロキシ−ｐ−クォーターフェニル類及びその製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005247809A JP2005247809A (ja) | 2005-09-15 |
| JP2005247809A5 JP2005247809A5 (enExample) | 2006-12-07 |
| JP4162615B2 true JP4162615B2 (ja) | 2008-10-08 |
Family
ID=35028641
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004064056A Expired - Fee Related JP4162615B2 (ja) | 2004-03-08 | 2004-03-08 | ４，４’’’−ジヒドロキシ−ｐ−クォ―ターフェニル類の製造方法。 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4162615B2 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5377935B2 (ja) * | 2008-11-11 | 2013-12-25 | 本州化学工業株式会社 | 新規なジヒドロキシクォーターフェニル化合物及びその原料化合物 |
| JP5551151B2 (ja) * | 2009-02-24 | 2014-07-16 | 本州化学工業株式会社 | 新規なエポキシ化合物 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0943873A (ja) * | 1995-07-26 | 1997-02-14 | Canon Inc | 電子写真感光体、及び該感光体を有する電子写真装置 |
| JP4041655B2 (ja) * | 2001-02-08 | 2008-01-30 | 本州化学工業株式会社 | ４，４”−ジヒドロキシ−ｐ−ターフェニル類の製造方法 |
-
2004
- 2004-03-08 JP JP2004064056A patent/JP4162615B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2005247809A (ja) | 2005-09-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4108946B2 (ja) | 新規な１，４−ビス（４−ヒドロキシフェニル）−１−シクロヘキセン類 | |
| JP4041655B2 (ja) | ４，４”−ジヒドロキシ−ｐ−ターフェニル類の製造方法 | |
| JP4162615B2 (ja) | ４，４’’’−ジヒドロキシ−ｐ−クォ―ターフェニル類の製造方法。 | |
| JP4829927B2 (ja) | ４，４’’’−ジヒドロキシ−ｐ−クォーターフェニル類及びその製造方法 | |
| JP5377935B2 (ja) | 新規なジヒドロキシクォーターフェニル化合物及びその原料化合物 | |
| EP0287290B1 (en) | Preparation process of 4,4'-biphenol, precursor of same and preparation process of precursor | |
| JP4115450B2 (ja) | 新規な４，４’−ジヒドロキシフェニル−ビシクロヘキセン類 | |
| JP4246427B2 (ja) | 新規な４，４”−ジヒドロキシ−ｐ−ターフェニル類 | |
| JP5752361B2 (ja) | １−（４−ヒドロキシフェニル）−１−シクロヘキセン類の製造方法 | |
| JP4757282B2 (ja) | ４，４”−ジヒドロキシ−ｐ−ターフェニル類 | |
| JP3001862B2 (ja) | テトラアルキルジフェノールの新規な製造方法 | |
| JP4693332B2 (ja) | 新規な４−置換フェニルフェノール類 | |
| JP4388839B2 (ja) | ４，４’’’−ジアルコキシ−ｐ−クォーターフェニル類及びその製造方法 | |
| KR890003786B1 (ko) | 4-히드록시바이페닐-4-카르복실산의 제조방법 | |
| JP2503038B2 (ja) | ４，４’−ビフェノ―ルの製造方法及びその前駆体並びに前駆体の製造方法 | |
| JP4786082B2 (ja) | 新規な４−置換シクロヘキシルフェノール類 | |
| JP4022381B2 (ja) | 新規な４−置換シクロヘキセニルフェノール類 | |
| JPS63190853A (ja) | ４’−ヒドロキシビフエニル−４−カルボン酸の製造方法 | |
| JP4959915B2 (ja) | 新規な４，４”−置換オキシ−ｐ−ターフェニル類 | |
| JP2516230B2 (ja) | ３，４’−ジヒドロキシビフェニルの製造方法 | |
| JP4022387B2 (ja) | 新規な４−置換シクロヘキシリデンビスフェノール類 | |
| JP2533565B2 (ja) | ３―（４―ヒドロキシフェニル）―シクロヘキサンカルボン酸及び４’―ヒドロキシビフェニル―３―カルボン酸の製造方法 | |
| JPS632938A (ja) | ４，４’−ビフエノ−ルの製造方法 | |
| JPS6314756A (ja) | ４′−ヒドロキシビフエニル−４−カルボン酸の製造方法 | |
| JPH01160930A (ja) | ４−（４−ヒドロキシフェニル）−シクロヘキサノール及び４，４’−ビフェノールの製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20061017 Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20061017 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20061017 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20071225 |
|
| A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20080222 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20080408 |
|
| A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20080606 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20080708 |
|
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
| A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20080606 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20080722 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110801 Year of fee payment: 3 |
|
| R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 Ref document number: 4162615 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20140801 Year of fee payment: 6 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |