JP2005336160A - ビスフェニル−2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルホスフィンオキシド誘導体およびその製造方法 - Google Patents
ビスフェニル−2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルホスフィンオキシド誘導体およびその製造方法 Download PDFInfo
- Publication number
- JP2005336160A JP2005336160A JP2004376435A JP2004376435A JP2005336160A JP 2005336160 A JP2005336160 A JP 2005336160A JP 2004376435 A JP2004376435 A JP 2004376435A JP 2004376435 A JP2004376435 A JP 2004376435A JP 2005336160 A JP2005336160 A JP 2005336160A
- Authority
- JP
- Japan
- Prior art keywords
- tetrafluoro
- represented
- oxide
- trifluoromethylphenylphosphine
- polyimide
- 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.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 22
- 229920001721 polyimide Polymers 0.000 claims abstract description 47
- 239000004642 Polyimide Substances 0.000 claims abstract description 46
- 239000000126 substance Substances 0.000 claims abstract description 34
- 239000000178 monomer Substances 0.000 claims abstract description 24
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 14
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000006243 chemical reaction Methods 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 19
- -1 3-nitrophenyl Chemical group 0.000 claims description 16
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 12
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 11
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 claims description 10
- MEAQATOLIZVMBQ-UHFFFAOYSA-N 1-diphenylphosphoryl-2,3,5,6-tetrafluoro-4-(trifluoromethyl)benzene Chemical compound FC1=C(C(F)(F)F)C(F)=C(F)C(P(=O)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1F MEAQATOLIZVMBQ-UHFFFAOYSA-N 0.000 claims description 7
- 150000004985 diamines Chemical class 0.000 claims description 7
- 150000003949 imides Chemical class 0.000 claims description 6
- 238000006116 polymerization reaction Methods 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 5
- 229910052763 palladium Inorganic materials 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 4
- QPQGTZMAQRXCJW-UHFFFAOYSA-N [chloro(phenyl)phosphoryl]benzene Chemical compound C=1C=CC=CC=1P(=O)(Cl)C1=CC=CC=C1 QPQGTZMAQRXCJW-UHFFFAOYSA-N 0.000 claims description 4
- 229910017604 nitric acid Inorganic materials 0.000 claims description 4
- DONVNRFILRLHJB-UHFFFAOYSA-N 1-bromo-2,3,5,6-tetrafluoro-4-(trifluoromethyl)benzene Chemical compound FC1=C(F)C(C(F)(F)F)=C(F)C(F)=C1Br DONVNRFILRLHJB-UHFFFAOYSA-N 0.000 claims description 3
- JCCUQYPRSYNESZ-UHFFFAOYSA-N FC1=C(C(=C(C(=C1[PH2]=O)F)F)C(F)(F)F)F Chemical compound FC1=C(C(=C(C(=C1[PH2]=O)F)F)C(F)(F)F)F JCCUQYPRSYNESZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- 238000006396 nitration reaction Methods 0.000 claims description 3
- 238000006467 substitution reaction Methods 0.000 claims description 3
- LJGHYPLBDBRCRZ-UHFFFAOYSA-N 3-(3-aminophenyl)sulfonylaniline Chemical group NC1=CC=CC(S(=O)(=O)C=2C=C(N)C=CC=2)=C1 LJGHYPLBDBRCRZ-UHFFFAOYSA-N 0.000 claims description 2
- 238000003747 Grignard reaction Methods 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- ATPGNTDARNWVLL-UHFFFAOYSA-N methylphosphonoylbenzene Chemical class CP(=O)C1=CC=CC=C1 ATPGNTDARNWVLL-UHFFFAOYSA-N 0.000 claims 1
- 238000005481 NMR spectroscopy Methods 0.000 description 21
- 238000004458 analytical method Methods 0.000 description 12
- 239000002904 solvent Substances 0.000 description 11
- 238000005160 1H NMR spectroscopy Methods 0.000 description 10
- QQGYZOYWNCKGEK-UHFFFAOYSA-N 5-[(1,3-dioxo-2-benzofuran-5-yl)oxy]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(OC=2C=C3C(=O)OC(C3=CC=2)=O)=C1 QQGYZOYWNCKGEK-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 239000007795 chemical reaction product Substances 0.000 description 10
- OYCLAICJOKGVKJ-UHFFFAOYSA-N 3-[(3-aminophenyl)-[2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl]phosphoryl]aniline Chemical class NC1=CC=CC(P(=O)(C=2C=C(N)C=CC=2)C=2C(=C(F)C(=C(F)C=2F)C(F)(F)F)F)=C1 OYCLAICJOKGVKJ-UHFFFAOYSA-N 0.000 description 9
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 238000005259 measurement Methods 0.000 description 8
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 229910052731 fluorine Inorganic materials 0.000 description 6
- 239000011737 fluorine Substances 0.000 description 6
- 230000009477 glass transition Effects 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 4
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
- 239000007818 Grignard reagent Substances 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 150000004795 grignard reagents Chemical class 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000004065 semiconductor Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- ZPRUMUVRIQQUIF-UHFFFAOYSA-N 1-bis(3-nitrophenyl)phosphoryl-2,3,5,6-tetrafluoro-4-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC=CC(P(=O)(C=2C=C(C=CC=2)[N+]([O-])=O)C=2C(=C(F)C(=C(F)C=2F)C(F)(F)F)F)=C1 ZPRUMUVRIQQUIF-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OERXHVXHIKSJSK-UHFFFAOYSA-N [O-][N+](C1=CC=CC(P(C2=CC([N+]([O-])=O)=CC=C2)C(C(F)=C(C(C(F)(F)F)=C2F)F)=C2F)=C1)=O Chemical compound [O-][N+](C1=CC=CC(P(C2=CC([N+]([O-])=O)=CC=C2)C(C(F)=C(C(C(F)(F)F)=C2F)F)=C2F)=C1)=O OERXHVXHIKSJSK-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical group 0.000 description 3
- 239000012776 electronic material Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- APXJLYIVOFARRM-UHFFFAOYSA-N 4-[2-(3,4-dicarboxyphenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl]phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(C(O)=O)C(C(O)=O)=C1 APXJLYIVOFARRM-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 125000006267 biphenyl group Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000010292 electrical insulation Methods 0.000 description 2
- 150000002222 fluorine compounds Chemical class 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000005462 imide group Chemical group 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- VNKSKFJVASDGBE-UHFFFAOYSA-N 3-[(3-aminophenyl)-phenylphosphoryl]aniline Chemical group NC1=CC=CC(P(=O)(C=2C=CC=CC=2)C=2C=C(N)C=CC=2)=C1 VNKSKFJVASDGBE-UHFFFAOYSA-N 0.000 description 1
- VQVIHDPBMFABCQ-UHFFFAOYSA-N 5-(1,3-dioxo-2-benzofuran-5-carbonyl)-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)=O)=C1 VQVIHDPBMFABCQ-UHFFFAOYSA-N 0.000 description 1
- QRCQQSHCWIURRK-UHFFFAOYSA-M Fc1c(F)c(c(F)c(F)c1[Mg]Br)C(F)(F)F Chemical compound Fc1c(F)c(c(F)c(F)c1[Mg]Br)C(F)(F)F QRCQQSHCWIURRK-UHFFFAOYSA-M 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000009529 body temperature measurement Methods 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000006575 electron-withdrawing group Chemical group 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000006358 imidation reaction Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- WKGDNXBDNLZSKC-UHFFFAOYSA-N oxido(phenyl)phosphanium Chemical class O=[PH2]c1ccccc1 WKGDNXBDNLZSKC-UHFFFAOYSA-N 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 238000001394 phosphorus-31 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920005575 poly(amic acid) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 description 1
- 239000003643 water by type 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/53—Organo-phosphine oxides; Organo-phosphine thioxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0246—Polyamines containing other atoms than carbon, hydrogen, nitrogen or oxygen in the main chain
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/53—Organo-phosphine oxides; Organo-phosphine thioxides
- C07F9/5325—Aromatic phosphine oxides or thioxides (P-C aromatic linkage)
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/5537—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom the heteroring containing the structure -C(=O)-N-C(=O)- (both carbon atoms belong to the heteroring)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
【解決手段】 一分子内に過フッ素化されたベンゼン置換体とホスフィンオキシドとが同時に置換された新規構造物質であって、ポリイミド本然の優れた熱的・機械的特性を保持するだけでなく、低い誘電常数と優れた接着性を有するポリイミド重合用単量体として有用なビスフェニル−2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルホスフィンオキシド誘導体およびその製造方法を提供する。
【選択図】図1
Description
M. F. Martinez-Nuez et al., Polymer Preprint, 35, p.709(1994)
a)有機溶媒およびマグネシウムの存在下で、前記化学式(2)で表される2,3,5,6−テトラフルオロ−4−トリフルオロメチルブロモベンゼンとジフェニルホスフィン酸クロリドとをグリニャール反応させて上記化学式(4)で表される2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルジフェニルホスフィンオキシド(7FPPO)を製造する段階、
b)上記化学式(4)で表される化合物(7FPPO)に硫酸と硝酸とでニトロ化させて上記化学式(5)で表されるビス(3−ニトロフェニル)−2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルホスフィンオキシド(DN7FPPO)を製造する段階、
c)上記化学式(5)で表される化合物(DN7FPPO)をパラジウム触媒の存在下で水素化させて上記化学式(6)で表されるビス(3−アミノフェニル)−2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルホスフィンオキシド(DA7FPPO)を製造する段階。
磁石攪拌機(magnetic stirrer)、添加用漏斗(addition funnel)、凝縮機(condenser)および窒素注入口(nitrogen inlet)付きの500mlの3つ口丸底フラスコを準備した。マグネシウムパウダー(Mg powder)(Aldrich社製)1.47gと蒸留精製されたテトラヒドロフラン(THF)(Aldrich社製)150mlを反応器に添加した。氷/塩水浴を用いて反応混合物の温度を−5℃以下に下げた後、2,3,5,6−テトラフルオロ−4−トリフルオロメチルブロモベンゼン(Fluorochem社製)15gを添加用漏斗を用いて徐々に約3時間にわたって添加し、溶液を常温に至らせた。反応物を常温で24時間さらに反応させてグリニャール試薬(Grignard reagent)である2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルマグネシウムブロミドを得た。
磁石攪拌機(magnetic stirrer)、添加用漏斗(addition funnel)、凝縮機(condenser)および窒素注入口(nitrogen inlet)付きの250mlの3つ口丸底フラスコを準備し、前記実施例1に係る方法で合成した化合物(7FPPO)7gと硫酸70mlを入れた後、常温で約30分間溶かした。次いで、氷/塩水浴(ice/salt bath)を用いて反応物が−10〜−5℃範囲の温度になるようにした後、硝酸2.4mlと硫酸10.5mlの混合溶液を添加用漏斗を通じて2時間にわたって徐々に添加した。反応物を常温に放置し、常温に至ると8時間さらに反応させた。反応が終結した後、反応生成物を1Kgの氷水に混合した後、混合物が常温に至ると重炭酸ナトリウム(NaHCO3)を用いて中和した後、クロロホルムと水を用いて抽出した。抽出物を沸騰無水エタノールに溶かして再結晶することによって、目的とするジニトロ化合物(DN7FPPO)7.5g(収率89%)を得た。
前記実施例2で合成されたジニトロ化合物(DN7FPPO)12g、無水エタノール150mlおよび10% Pd/C15mgを高圧反応器(high pressure reactor)に入れた後、100psi水素圧および50℃の反応条件で24時間反応させた。反応生成物をセライト(celite)を用いてプラジウム(Pd/C)をろ過した後、溶媒を蒸発させ、これをさらにカラムクロマトグラフィー方法で精製して目的とするジアミン化合物(DA7FPPO;収率83%)を得た。
機械的攪拌機(Mechanical stirrer)、凝縮機(condenser)および窒素注入口(nitrogen inlet)付きの250mlの3つ口丸底フラスコを準備した。前記実施例3で得られたジアミン化合物(DA7FPPO)6.1g(13.64mmol)と蒸留精製された1−メチル−2−ピロリドン(NMP)[Fluka社製]50mlを反応器に入れた。DA7FPPOを完全に溶かした後、無水フタル酸 (PA)[Aldrich社製]0.16g(1.10mmol)と2,2−ビス(3,4−ジカルボキシフェニル)ヘキサフルオロプロパン二無水物(6FDA)[Chriskev社製]5.82g(13.09mmol)を順次反応器に添加した後、反応物を常温で24時間反応させた。
複屈折率(△n )=nTE−nTM
(式中、nTEはrefractive index of in-plane、nTMはrefractive index of out-of-planeである。)
Claims (3)
- 下記の製造段階が含まれることを特徴とするビスフェニル−2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルホスフィンオキシド誘導体の製造方法。
a)有機溶媒およびマグネシウムの存在下で、下記化学反応式の化学式(2)で表される2,3,5,6−テトラフルオロ−4−トリフルオロメチルブロモベンゼンと下記化学反応式の化学式(3)で表されるジフェニルホスフィン酸クロリドとをグリニャール反応させて下記化学反応式の化学式(4)で表される2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルジフェニルホスフィンオキシド(7FPPO)を製造する段階、
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020040038476A KR100591983B1 (ko) | 2004-05-28 | 2004-05-28 | 비스페닐-2,3,5,6-테트라플루오로-4-트리플루오로메틸페닐포스핀 옥사이드 유도체와 이의 제조방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2005336160A true JP2005336160A (ja) | 2005-12-08 |
JP4176074B2 JP4176074B2 (ja) | 2008-11-05 |
Family
ID=35426277
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004376435A Expired - Fee Related JP4176074B2 (ja) | 2004-05-28 | 2004-12-27 | ビスフェニル−2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルホスフィンオキシド誘導体およびその製造方法 |
Country Status (4)
Country | Link |
---|---|
US (1) | US7169879B2 (ja) |
JP (1) | JP4176074B2 (ja) |
KR (1) | KR100591983B1 (ja) |
DE (1) | DE102004063360B4 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009221309A (ja) * | 2008-03-14 | 2009-10-01 | Manac Inc | 含リンエステル基含有テトラカルボン酸またはその二無水物及び含リンポリエステルイミド |
JP2011173806A (ja) * | 2010-02-23 | 2011-09-08 | Manac Inc | リン含有ジアミン化合物および難燃性ポリイミド |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100731125B1 (ko) * | 2005-12-28 | 2007-06-22 | 동부일렉트로닉스 주식회사 | 씨모스 이미지 센서 |
CN104356383B (zh) * | 2014-10-17 | 2017-01-18 | 常州大学 | 一类同时含四大取代侧基和扭曲非共平面结构聚酰亚胺及其制备方法 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5482596A (en) * | 1994-01-27 | 1996-01-09 | Albemarle Corporation | Mixed ligand catalyst for preparing aryl-substituted aliphatic carboxylic esters |
DE4447068A1 (de) * | 1994-12-29 | 1996-07-04 | Hoechst Ag | Verfahren zur Herstellung aromatischer Olefine |
DE19647582A1 (de) * | 1996-11-18 | 1998-05-20 | Hoechst Ag | Verfahren zur Herstellung von aromatischen Olefinen mittels Katalyse durch Palladaphosphacyclobutane |
KR100329283B1 (ko) * | 1999-11-16 | 2002-03-18 | 김효근 | 불소 함유 치환체를 가진 트리아릴포스핀 옥사이드 유도체 |
KR100419854B1 (ko) * | 2001-01-15 | 2004-02-25 | 광주과학기술원 | 불소 치환체를 함유한 트리아릴포스핀옥사이드 유도체 및그 제조방법 |
-
2004
- 2004-05-28 KR KR1020040038476A patent/KR100591983B1/ko not_active IP Right Cessation
- 2004-12-17 US US11/016,293 patent/US7169879B2/en not_active Expired - Fee Related
- 2004-12-27 JP JP2004376435A patent/JP4176074B2/ja not_active Expired - Fee Related
- 2004-12-30 DE DE102004063360A patent/DE102004063360B4/de not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009221309A (ja) * | 2008-03-14 | 2009-10-01 | Manac Inc | 含リンエステル基含有テトラカルボン酸またはその二無水物及び含リンポリエステルイミド |
JP2011173806A (ja) * | 2010-02-23 | 2011-09-08 | Manac Inc | リン含有ジアミン化合物および難燃性ポリイミド |
Also Published As
Publication number | Publication date |
---|---|
KR100591983B1 (ko) | 2006-06-20 |
DE102004063360B4 (de) | 2007-04-26 |
US20050267317A1 (en) | 2005-12-01 |
KR20050112999A (ko) | 2005-12-01 |
JP4176074B2 (ja) | 2008-11-05 |
US7169879B2 (en) | 2007-01-30 |
DE102004063360A1 (de) | 2005-12-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Jeong et al. | Synthesis and characterization of novel polyimides containing fluorine and phosphine oxide moieties | |
Liu et al. | Poly (aryl ether ketone) s with (3‐methyl) phenyl and (3‐trifluoromethyl) phenyl side groups | |
CN113412299B (zh) | 聚酰胺酸和聚酰亚胺、光学薄膜和显示装置、以及它们的制造方法 | |
JP2007091701A (ja) | フルオレニル基およびエステル基を含有するテトラカルボン酸類、フルオレニル基含有ポリエステルイミド前駆体、およびフルオレニル基含有ポリエステルイミド、ならびにこれらの製造方法 | |
JP6635506B2 (ja) | フルオレン骨格を有するジアミン、ポリアミック酸、及びポリイミド | |
Myung et al. | Synthesis and characterization of novel polyimides with 2, 2‐bis [4 (4‐aminophenoxy) phenyl] phthalein‐3′, 5′‐bis (trifluoromethyl) anilide | |
Wang et al. | New fluorinated poly (ether sulfone imide) s with high thermal stability and low dielectric constant | |
Wu et al. | Novel soluble and optically active polyimides containing axially asymmetric 9, 9′-spirobifluorene units: synthesis, thermal, optical and chiral properties | |
JP7096931B2 (ja) | フッ素化アミド化合物、フッ素化含窒素複素環含有化合物およびフッ素化化合物 | |
Kwak et al. | Synthesis and characterization of polyimides from bis (3‐aminophenyl)‐4‐(1‐adamantyl) phenoxyphenyl phosphine oxide | |
Zhang et al. | Polyimides with low dielectric constants and dissipation factors at high frequency derived from novel aromatic diamines with bistrifluoromethyl pendant groups | |
JP5546210B2 (ja) | 芳香族ジアミン化合物及びその製造方法並びに合成樹脂 | |
US6342638B1 (en) | Triarylphosphine oxide derivatives containing fluorine substituents | |
Jiang et al. | Synthesis and characterization of organo‐soluble polyimides derived from a new spirobifluorene diamine | |
JP4176074B2 (ja) | ビスフェニル−2,3,5,6−テトラフルオロ−4−トリフルオロメチルフェニルホスフィンオキシド誘導体およびその製造方法 | |
Lee et al. | Synthesis and characterization of polyimides from bis (3-aminophenyl)-2, 3, 5, 6-tetrafluoro-4-trifluoromethylphenyl phosphine oxide (mDA7FPPO) | |
JP6268959B2 (ja) | 含フッ素重合性単量体およびそれを用いた高分子化合物 | |
Kausar et al. | Facile synthesis and properties of a new generation of soluble and thermally stable polyimides | |
WO2022030447A1 (ja) | 含フッ素ジアミンまたはその塩、含フッ素ジアミンまたはその塩の製造方法、ポリアミド、ポリアミドの製造方法、ポリアミド溶液、ポリアミド環化体、ポリアミド環化体の製造方法、高周波電子部品用絶縁材、高周波電子部品用絶縁材の製造方法、高周波電子部品、高周波機器および高周波電子部品製造用絶縁材料 | |
JP2947691B2 (ja) | 芳香族ジアミンおよびポリイミド、ならびにこれらの製造方法 | |
KR100542296B1 (ko) | 포스핀옥사이드와 아다만탄이 동시에 치환되어 있는비스페닐-1-아다만틸포스핀옥사이드 유도체와 이의 제조방법 | |
JP3867983B2 (ja) | フェニルエチニル基を有するジアミンモノマー | |
KR100594566B1 (ko) | 아다만탄과 포스핀 옥사이드를 함유하는 비스페닐 아다만틸페녹시페닐 포스핀 옥사이드 유도체와 이의 제조방법 | |
JP6462236B2 (ja) | ポリイミドおよび耐熱性フィルム | |
KR101509316B1 (ko) | 폴리이미드, 이의 제조방법 및 상기 폴리이미드를 포함하는 필름 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20041227 |
|
RD01 | Notification of change of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7426 Effective date: 20050105 |
|
A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20050105 |
|
TRDD | Decision of grant or rejection written | ||
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20080723 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20080729 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20080819 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110829 Year of fee payment: 3 |
|
R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120829 Year of fee payment: 4 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120829 Year of fee payment: 4 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130829 Year of fee payment: 5 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
LAPS | Cancellation because of no payment of annual fees |