CN1771087A - Method for preparing bisphenol catalysts and bisphenols - Google Patents
Method for preparing bisphenol catalysts and bisphenols Download PDFInfo
- Publication number
- CN1771087A CN1771087A CN03826406.4A CN03826406A CN1771087A CN 1771087 A CN1771087 A CN 1771087A CN 03826406 A CN03826406 A CN 03826406A CN 1771087 A CN1771087 A CN 1771087A
- Authority
- CN
- China
- Prior art keywords
- carbon atoms
- contain
- functional group
- ring
- phenol
- 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
- 229930185605 Bisphenol Natural products 0.000 title claims abstract description 72
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 title claims abstract description 67
- 239000003054 catalyst Substances 0.000 title claims abstract description 27
- 238000000034 method Methods 0.000 title claims description 93
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 title abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 56
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000002253 acid Substances 0.000 claims abstract description 14
- 239000011973 solid acid Substances 0.000 claims abstract description 10
- 239000002952 polymeric resin Substances 0.000 claims abstract 3
- 229920003002 synthetic resin Polymers 0.000 claims abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 308
- 125000000524 functional group Chemical group 0.000 claims description 116
- 125000001931 aliphatic group Chemical group 0.000 claims description 107
- -1 aromatic hydroxy compound Chemical class 0.000 claims description 76
- 125000003118 aryl group Chemical group 0.000 claims description 74
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 60
- 229910052799 carbon Inorganic materials 0.000 claims description 58
- 229910052739 hydrogen Inorganic materials 0.000 claims description 55
- 239000001257 hydrogen Substances 0.000 claims description 55
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 48
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 47
- 125000005587 carbonate group Chemical group 0.000 claims description 43
- 150000002148 esters Chemical group 0.000 claims description 43
- 125000001743 benzylic group Chemical group 0.000 claims description 41
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 38
- 150000001875 compounds Chemical class 0.000 claims description 38
- 150000001721 carbon Chemical group 0.000 claims description 37
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 34
- 125000002723 alicyclic group Chemical group 0.000 claims description 26
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims description 26
- 229920005989 resin Polymers 0.000 claims description 21
- 239000011347 resin Substances 0.000 claims description 21
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 20
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 17
- 239000005864 Sulphur Substances 0.000 claims description 15
- 125000001072 heteroaryl group Chemical group 0.000 claims description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 14
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 13
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 13
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 13
- 125000004104 aryloxy group Chemical group 0.000 claims description 13
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 13
- 229910052794 bromium Inorganic materials 0.000 claims description 13
- 239000000460 chlorine Substances 0.000 claims description 13
- 229910052801 chlorine Inorganic materials 0.000 claims description 13
- 229910052731 fluorine Inorganic materials 0.000 claims description 13
- 239000011737 fluorine Substances 0.000 claims description 13
- 229920002554 vinyl polymer Polymers 0.000 claims description 13
- 238000006555 catalytic reaction Methods 0.000 claims description 10
- 150000002576 ketones Chemical class 0.000 claims description 9
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- 150000001299 aldehydes Chemical class 0.000 claims description 7
- 125000002883 imidazolyl group Chemical group 0.000 claims description 7
- ZRALSGWEFCBTJO-UHFFFAOYSA-N guanidine group Chemical group NC(=N)N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 150000002460 imidazoles Chemical class 0.000 claims description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 150000001735 carboxylic acids Chemical class 0.000 claims description 4
- 230000007935 neutral effect Effects 0.000 claims description 4
- 125000002743 phosphorus functional group Chemical group 0.000 claims description 4
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 32
- 150000002431 hydrogen Chemical class 0.000 claims 20
- 229920002313 fluoropolymer Polymers 0.000 claims 9
- 239000004811 fluoropolymer Substances 0.000 claims 9
- 239000004793 Polystyrene Substances 0.000 claims 4
- 229910021536 Zeolite Inorganic materials 0.000 claims 4
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 4
- 229920002223 polystyrene Polymers 0.000 claims 4
- 239000010457 zeolite Substances 0.000 claims 4
- 239000010458 rotten stone Substances 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 2
- 235000003140 Panax quinquefolius Nutrition 0.000 claims 2
- 240000005373 Panax quinquefolius Species 0.000 claims 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 2
- 125000005910 alkyl carbonate group Chemical group 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical group CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 claims 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical group CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 2
- 150000004693 imidazolium salts Chemical class 0.000 claims 1
- 150000003222 pyridines Chemical class 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 229940106691 bisphenol a Drugs 0.000 abstract description 6
- 238000004519 manufacturing process Methods 0.000 abstract description 6
- 229910052717 sulfur Inorganic materials 0.000 abstract description 3
- 239000011593 sulfur Substances 0.000 abstract description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 abstract 1
- 125000004354 sulfur functional group Chemical group 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 19
- 239000000203 mixture Substances 0.000 description 17
- 239000007788 liquid Substances 0.000 description 10
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 9
- 150000002894 organic compounds Chemical class 0.000 description 7
- 238000006482 condensation reaction Methods 0.000 description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 230000005595 deprotonation Effects 0.000 description 5
- 238000010537 deprotonation reaction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 125000006239 protecting group Chemical group 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 229920003053 polystyrene-divinylbenzene Polymers 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- UFULAYFCSOUIOV-UHFFFAOYSA-N cysteamine Chemical compound NCCS UFULAYFCSOUIOV-UHFFFAOYSA-N 0.000 description 2
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229960003151 mercaptamine Drugs 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000011949 solid catalyst Substances 0.000 description 2
- 239000008247 solid mixture Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000003573 thiols Chemical class 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- FARSPAVQUKTXLF-UHFFFAOYSA-N 1h-benzimidazol-1-ium;chloride Chemical compound Cl.C1=CC=C2NC=NC2=C1 FARSPAVQUKTXLF-UHFFFAOYSA-N 0.000 description 1
- FGWADSPDFGXDHR-UHFFFAOYSA-N 5-aminopentane-1-thiol;hydrochloride Chemical compound Cl.NCCCCCS FGWADSPDFGXDHR-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 238000007171 acid catalysis Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000004703 alkoxides Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- UVCBVNDFDCGFKI-UHFFFAOYSA-N benzene;carbonic acid Chemical compound OC(O)=O.C1=CC=CC=C1 UVCBVNDFDCGFKI-UHFFFAOYSA-N 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- VBQDSLGFSUGBBE-UHFFFAOYSA-N benzyl(triethyl)azanium Chemical compound CC[N+](CC)(CC)CC1=CC=CC=C1 VBQDSLGFSUGBBE-UHFFFAOYSA-N 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- HRKQOINLCJTGBK-UHFFFAOYSA-N dihydroxidosulfur Chemical compound OSO HRKQOINLCJTGBK-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000007337 electrophilic addition reaction Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- BMXFPSYOCKSSBE-UHFFFAOYSA-N guanidine Chemical group NC(N)=N.NC(N)=N BMXFPSYOCKSSBE-UHFFFAOYSA-N 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 125000001741 organic sulfur group Chemical group 0.000 description 1
- YSWYYGKGAYSAOJ-UHFFFAOYSA-N phosphane Chemical group P.P YSWYYGKGAYSAOJ-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920006009 resin backbone Polymers 0.000 description 1
- 238000009666 routine test Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur atoms
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0215—Sulfur-containing compounds
- B01J31/0217—Mercaptans or thiols
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0215—Sulfur-containing compounds
- B01J31/0218—Sulfides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
- B01J31/0235—Nitrogen containing compounds
- B01J31/0244—Nitrogen containing compounds with nitrogen contained as ring member in aromatic compounds or moieties, e.g. pyridine
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
- B01J31/0255—Phosphorus containing compounds
- B01J31/0267—Phosphines or phosphonium compounds, i.e. phosphorus bonded to at least one carbon atom, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, the other atoms bonded to phosphorus being either carbon or hydrogen
- B01J31/0268—Phosphonium compounds, i.e. phosphine with an additional hydrogen or carbon atom bonded to phosphorous so as to result in a formal positive charge on phosphorous
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
- B01J31/0271—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds also containing elements or functional groups covered by B01J31/0201 - B01J31/0231
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/06—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing polymers
- B01J31/08—Ion-exchange resins
- B01J31/10—Ion-exchange resins sulfonated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
- C07C37/20—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms using aldehydes or ketones
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/32—Sulfur atoms
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- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/84—Sulfur atoms
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- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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Abstract
This disclosure relates to a method for producing and using catalysts in the production of bisphenols, and in particular to a method for producing catalysts which contain poly-sulfur mercaptan promoters, and using these catalysts in the production of bisphenol-A and its derivatives. The poly-sulphur groups are pendant fro a positively charged functionality comprising nitrogen or phosphorous, preferably a nitrogen heterocycle. The catalysts also comprise a solid acid support component comprising a protic acid functionality, preferably a sulfonated polymeric resin.
Description
Background of invention
The present invention relates to prepare and use the method for the catalyst that is used for bisphenol production, particularly relate to the method that preparation contains the catalyst of poly-sulphur mercaptan promoter (poly-sulfur mercaptan promoters), and in producing bisphenol-A and its derivative, use these catalyst.
Typical bis-phenol is as 4,4 '-isopropylidene bis-phenol, and for example bisphenol-A (BPA) is used for synthesizing polymeric material as monomer widely, as the engineered thermoplastic material.For instance, BPA is exactly a principal monomer of producing Merlon.Bis-phenol is normally made on aromatic hydroxy compound such as phenol as the acetone electrophilic addition by aldehydes or ketones in the presence of the acidic catalyst composition.The reaction of these types is also referred to as the condensation reaction under the acid catalysis.Industrial, after sulfonated polystyrene ion exchange resin and the divinyl benzene crosslinked, for example PS-DVB is common as the solid acid composition in the carbon monoxide-olefin polymeric.Reaction promoter also can be as reaction rate and the selectivity of a part to improve required condensation reaction in the carbon monoxide-olefin polymeric.In the example of BPA, needed selectivity is contraposition-para-isomer (pp-BPA).The molecular forms that promoter can not followed in bulk reaction matrix exists, as " body-promoter (bulk-promoters) "; Also can be linked at form on the resin by ionic bond, as " then-promoter (attached-promoters) ".The useful promoter of one class is mercaptan, particularly thio-alcohol (thiols), for example derivative of this hydrogen sulfide of organosulfur compound.Typical mercaptan promoter only contains a sulphur atom, and the long-pending composition of the catalysis of formation forms bis-phenol catalysis has very low isomers selectivity.Under the situation of BPA, do not wish to form the isomers (op-BPA) of ortho position-contraposition.Therefore exist for a long time and what do not solve is a kind of new, improved carbon monoxide-olefin polymeric, and the method for preparing this carbon monoxide-olefin polymeric, they have selectivity to producing bis-phenol.The invention provides the method that preparation contains the carbon monoxide-olefin polymeric of poly-sulphur mercaptan promoter.Selectivity when in carbon monoxide-olefin polymeric, using poly-sulphur mercaptan to improve bis-phenol formation greatly.
Summary of the invention
In one embodiment, content disclosed by the invention relates to the method for preparing carbon monoxide-olefin polymeric, this catalyst can the catalysis aromatic hydroxy compound and the carbonyl containing compound reaction form bis-phenol, described method comprises the then step on the solid acid carrier component that contains functionalized protonic acid of poly-sulphur mercaptan promoter component, above-mentioned poly-sulphur mercaptan promoter component has structure (I)
R wherein
1Be to be selected from following functional group (functionality): guanidine (guanidinium) functional group of the ammonium functional group of positively charged, positively charged, phosphorus (phosphonium) functional group and the neutral amine of positively charged;
Wherein a is about 0 to about 11;
Wherein b is about 1 to about 11;
Wherein c is about 1 to about 11;
Wherein d is about 1 to about 5;
Wherein X connects functional group, is to be selected from a kind of in following: contain the 1 linear aliphatic chain to about 11 carbon atoms of having an appointment, contain aliphatic ring at least about 5 carbon atoms, contain aromatic ring at least about 6 carbon atoms, contain at least about the aliphatic heterocycle of 3 carbon atoms and contain heteroaromatic at least about 3 carbon atoms;
Wherein Y connects functional group, is to be selected from a kind of in following: contain the 1 linear aliphatic chain to about 11 carbon atoms of having an appointment, contain aliphatic ring at least about 5 carbon atoms, contain aromatic ring at least about 6 carbon atoms, contain at least about the aliphatic heterocycle of 3 carbon atoms and contain heteroaromatic at least about 3 carbon atoms;
R wherein
2Be to be selected from least a in following: hydrogen, uncle's aliphatic functionality, ester functional group, carbonate functionalities and the benzylic functionalities of following by benzyl Central Asia methine carbon atom.
In another embodiment, the invention discloses the method that forms bis-phenol, being included in carbon monoxide-olefin polymeric exists down, with the step of aromatic hydroxy compound with the compound reaction that contains carbonyl, described carbon monoxide-olefin polymeric comprises solid acid component and has the poly-sulphur mercaptan promoter component of following structure:
R wherein
1Be to be selected from following functional group: the phosphorus functional group and the neutral amine of the ammonium functional group of positively charged, the guanidine functional group of positively charged, positively charged;
Wherein a is about 0 to about 11;
Wherein b is about 1 to about 11;
Wherein c is about 1 to about 11;
Wherein d is about 1 to about 5;
Wherein X connects functional group, is to be selected from a kind of in following: contain the 1 linear aliphatic chain to about 11 carbon atoms of having an appointment, contain aliphatic ring at least about 5 carbon atoms, contain aromatic ring at least about 6 carbon atoms, contain at least about the aliphatic heterocycle of 3 carbon atoms and contain heteroaromatic at least about 3 carbon atoms;
Wherein Y connects functional group, is to be selected from a kind of in following: contain the 1 linear aliphatic chain to about 11 carbon atoms of having an appointment, contain aliphatic ring at least about 5 carbon atoms, contain aromatic ring at least about 6 carbon atoms, contain at least about the aliphatic heterocycle of 3 carbon atoms and contain heteroaromatic at least about 3 carbon atoms;
R wherein
2Be to be selected from least a in following: hydrogen, uncle's aliphatic functionality, ester functional group, carbonate functionalities and the benzylic functionalities of following by benzyl Central Asia methine carbon atom.
Detailed Description Of The Invention
Content disclosed by the invention relates to preparation and uses and produce used catalyst in the bis-phenol, be applicable to prepare then-promoter catalyst (attached-promoter catalysts) that this catalyst effectively catalyze aromatic hydroxy compounds generates bis-phenol with the compound reaction that contains carbonyl.Among the present invention, term " catalyst (catalysts) " is meant composition (composition), and wherein the various independent composition in the composition is called component (components).In this article, typical catalyst comprises polymeric material normally and is also referred to as " carrier (the support) " component that contains functionalized protonic acid group of " resin (resin) ", and " promoter (promoters) " component of organic compound normally.In this article, term " functional group (functionality) " is defined as one group of atom of atom or unit form, and their existence makes the molecule that connects this functional group have certain specific character.Herein, " functionalized protonic acid group " refers to one group of atom on the carrier component that is connected catalyst with covalent bond, can play proton source, for example Broensted acid, and by the deprotonation effect, relative anion can be as the anionicsite of the ionic bond of the promoter component of positively charged.The example that carrier component is suitable is and polystyrene resin up to 12% divinyl benzene crosslinked.The suitable example of the functionalized protonic acid group of following with carrier component is the sulfonic acid functional group, and it generates sulfonic acid anion functional group by the deprotonation effect; Phosphoric acid functional group, it generates phosphate anion functional group by the deprotonation effect; Carboxylic acid functional, it generates carboxylate anion functional group by the deprotonation effect.For example, In one embodiment of the present invention, carrier component is the polystyrene resin with 4% divinyl benzene crosslinked, and functionalized with sulfonic group.
Promoter component normally can form the organic compound of stable cationic part easily.Typical promoter component comprises at least one mercaptan chain functionality and the organic backbone functional group covalently bound with mercaptan chain functionality.Term used herein " mercaptan chain functionality (mercaptan chainfunctionality) " refers to organic sulfur functional group, and it is the derivative of hydrogen sulfide.In the present invention is open, typical mercaptan chain functionality, promptly-{ [(X)
a-S]
b-(Y)
c-S-R} comprises at least 2 sulphur atoms.The sulphur atom that exists in a mercaptan chain can reach 12 in one embodiment, for example in formula-{ [(X)
a-S]
b-(Y)
cB is about 1 to about 12 in the chain of-S-R} definition.Sulphur atom in the typical mercaptan chain functionality is connected with Y as X by various organic connection functional groups (organic linkers functionalities).In the present invention is open, the typical functional group that connects comprises, but be not limited to, comprise about 1 linear aliphatic chain to about 11 carbon atoms, contain at least 5 carbon atoms cycloaliphatic ring, contain at least 6 carbon atoms aromatic rings, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the aromatic heterocycle of at least 3 carbon atoms.Term " organic backbone functional group " is defined as organo-functional group, and it can form covalent bond with at least one mercaptan chain functionality, and can form stable cationic moiety, and this part can be as the cationic moiety of ionic bond.Suitable organic backbone functional group includes, but are not limited to, alkylammonium functional group, alkyl guanidine functional group, alkyl phosphorus functional group and amido functional group.Typical amino skeletal functionalities includes, but are not limited to monocyclic aromatic amino-compound and Ppolynuclear aromatic amino-compound.For example suitable amino skeletal functionalities includes, but are not limited to, pyridine functional groups, benzimidazole functional group, benzothiazole functional group and imidazoles functional group.When skeletal functionalities comprised member ring systems, mercaptan chain functionality can be keyed on this member ring systems on arbitrary position of covalency keyed jointing on this ring.For example for pyridine-mercaptan promoter, thiol functionalities can be connected on arbitrary position among 2,3 or 4 of pyridine ring.In addition, in each class of above-mentioned mercaptan promoter, promptly can there be not only mercaptan chain in alkylammonium mercaptans, alkyl guanidine mercaptan, alkyl phosphorus mercaptan and amineothiot in the promoter.For example, for pyridine mercaptan, pyridine ring can be replaced up to 5 mercaptan chain functionality, and chain covalent bond is received on each position of five carbocyclic ring positions of pyridine ring.
Usually the substituted radical with the R representative can be connected to electrical property, space structure and the binding ability thereof of regulating promoter on the promoter equally in chemical formula, thereby influences the activity of whole carbon monoxide-olefin polymeric.The promoter substituting group that is fit to comprises, but be not limited to, hydrogen, fluorine (fluoride), bromine (bromide), chlorine (chloride), vinyl, contain about 1 alkoxyl to about 11 carbon atoms (alkoxide) functional group, contain aryloxy group (aryloxide) functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain the aromatic series functional group at least about 6 carbon atoms hydroxyl (hydroxide).For the amineothiot that comprises member ring systems, substituting group also can be to contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring to be fused to amino ring by the adjacent ring substituting group and to go up or contain aromatic ring family ring at least about 6 carbon atoms, and described aromatic ring family ring is connected on the amino ring by the adjacent ring substituting group.
Being connected normally by ionic bond of promoter component and polymer support component finished, Yi Bian be positively charged promoter component, obtains by nitrogen-atoms is protonated as amineothiot; Another side is a deprotonation acid functional group electronegative on the resin backbone.The connection procedure of amineothiot promoter and acid-functionalized polymer support can carry out in aqueous solution.The term here " aqueous solution " comprises with the solution of water as solvent.For instance, the mercaptan promoter of protectiveness is as promoter [2-((CH
2)
2-S-(CH
2)
3-S-(t-Bu)) pyridine] can pass through [2-((CH by in water, mixing with the PS-DVB resin
2)
2-S-(CH
2)
3-S-(t-Bu)) pyridine]
+Azochlorosulfonate acid anion on cation and the polymer support passes through to form ionic bond, and promoter is connected on the PS-DVB resin of sulfonic acid functional.Perhaps, amineothiot promoter also can be connected on the acid-functionalized polymer support in the organic media that contains aromatic hydroxy compound such as phenol.
In an embodiment disclosed by the invention, mercaptan promoter with typically being used to protect the protecting group functional group of 16 family's elements such as oxygen and sulphur that sulphur atom is protected, was avoided oxidation before being connected on the carrier.Term used herein " protecting group " refers to the functional group that can prevent the particular type reaction, in this article, exists to be connected to the protecting group on the terminal sulphur atom in the mercaptan promoter, and purpose is in order to suppress the oxidation of terminal sulphur atom.Generally speaking, without the mercaptan sulfur alcohol moiety of protection synthetic or under promoter and condition that polymer support is connected, be oxidized to disulphide easily or by the higher degree oxidation.Herein, the example of the sulfur protecting group group that is fit to includes, but are not limited to, and forms aliphatic functionality, ester functional group, carbonate functionalities, the benzylic functionalities (benzylic functionalities) of stablizing carbocation (carbocations).When term " aliphatic " and term " protecting group " coupling, " aliphatic " refer to contain hydrogen atom and carbon atom become the side chain form can form the organic compound of stablizing carbonium ion.For example, in one embodiment, the aliphatic protecting group is the tert-butyl group-C (CH
3)
3But when term " aliphatic " and term " substituting group " coupling, " aliphatic " then refers to the more organic compound that contains hydrogen atom and carbon atom of broad sense, and this organic compound contains has an appointment 1 to about 11 carbon atoms, becomes linear or branching form.In addition, when term " aromatic series " and term " substituting group " coupling, the organic compound that contains hydrogen atom and carbon atom that " aromatic series " then refers to wherein contains at least about 6 ring conjugation carbon atoms.
The example of the ester functional group that is fit to, for example-C (O) R, wherein R can be aliphatic substituting group or aromatic substituents, it comprises and contains 1 those esters to about 11 carbon atoms of having an appointment, as acetate, for example-C (O) CH
3The example of the carbonate functionalities that is fit to, for example-C (O) OR, comprise carbonic ester with aliphatic or aromatic substituents.The example of the aliphatic acid ester carbonate protecting group that is fit to can be the tert-butoxy carbonic ester, for example-and C (O) O-
tBu.The example such as the benzol carbonate of the aromatic carbonate protecting group that is fit to, for example-C (O) OPh.The example of the benzylic functionalities that is fit to for example-CH
2(aryl) comprises those benzyl groups of containing at least 7 carbon atoms, as benzyl, for example-CH
2(C
6H
6).
In another embodiment, this paper also relates to and uses above-mentioned catalyst to form bis-phenol as 4 with catalysis, the method for 4 '-isopropylidene bis-phenol.Term herein " catalysis ", when it is relevant with carbon monoxide-olefin polymeric, refer to and in the reaction of the special transition of one or more chemicals, make on its reaction rate or the selectivity under the particular series reaction condition, had greatly improved, reaction rate or selectivity are more than or equal to the predetermined reference reaction rate or with reference to selectivity.Be the condensation reaction that forms bis-phenol between aromatic hydroxy compound and the compound that contains carbonyl by the reaction of catalysis herein, it carries out in liquid reaction mixture usually.The term here " liquid reaction mixture " refers to the mixture at the main down compound that exists with liquid state of normal temperature and pressure (for example about 25 ℃ and about 0.1MPa).Liquid reaction mixture can be heterogeneous in one homogeneous liquid mixture (homogeneous liquid mixtures) (for example two-phase liquid reaction mixture), also can be the liquid-solid mixture (heterogeneous liquid-solid mixtures) (for example sediment) that contains the out-phase of the component that solid state exists.
Producing the component that exists in the liquid reaction mixture of bis-phenol in typical condensation reaction comprises, but be not limited to, soluble component in the bis-phenol of required bis-phenol, the accessory substance of condensation reaction such as water, non-required bis-phenol, the soluble constituent of carbon monoxide-olefin polymeric, the carbon monoxide-olefin polymeric and unreacted raw material are aromatic hydroxy compound and carboxylic compound for example.The aromatic hydroxy compound that is fit to type includes, but are not limited to, and contains the monocycle aromatic of at least one hydroxyl or contains the poly-ring aromatic compounds of at least one hydroxyl.The aromatic hydroxy compound illustrative examples that is fit to includes, but are not limited to phenol, alkylphenol, alkoxy phenol, naphthols, alkyl naphthol and alkoxynaphthols.Here the term of the usefulness organic compound that compound refers to that " contains carbonyl " contains the sp that forms two keys with oxygen
2The carbon atom of hydridization comprises aldehyde and ketone.The example of suitable aldehyde is an acetaldehyde, and the example of suitable ketone is an acetone.
The various reaction conditions that influence condensation reaction comprise, but be not limited to, the various component weight percentage of the pH value of reaction vessel pressure, reaction temperature, stir speed (S.S.), reactant mixture, catalyst concn, liquid reaction mixture, include, but are not limited to the percetage by weight of aromatic hydroxy compound, the percetage by weight that contains the compound of carbonyl, the percetage by weight of required bis-phenol, the percetage by weight of water.For example use the reaction condition of the catalytic production BPA that above-mentioned catalyst carries out in increment flowing reactive still (incremental flow reactor) to comprise, but be not limited to, about 55 ℃ to about 85 ℃ of temperature, acetone concentration about 1% to about 10%, the about 0.1 pound of raw material of space velocity/pound solid catalyst per hour to 10 pounds of raw materials/the pound solid catalyst per hour.
Following embodiment comprises in the present invention provides further guidance those of ordinary skills are implemented the present invention's content required for protection.These embodiment that provided only are some representatives of the disclosure of invention.Therefore, following embodiment and be not used in restriction by any way as defined disclosure of the present invention in the claims.
Embodiment in the table 1: for each embodiment in the table 1, following synthesis program is used for the catalyst of preparation table 1, has promoter listed in the table 1.About 30mg is heated to about 70 ℃ to the phenol of the Rohm and Haas A131 resin particle (with the sulfonated polystyrene of about 4% divinyl benzene crosslinked) of about 55mg drying and the fusion of 4 times of quality, kept about one hour.Add the phenol solution of 540mM promoter again in mixture, consumption is enough to reach reactant mixture, about 1mmol promoter/every gram dried resin.Mixture continues to stir about 4 hours subsequently, and a part of afterwards phenol is removed.At this moment the catalyst mix amount in the phenol approximately is 3.5 times of dried resin quality when just having begun.In order to prove the as above catalytic performance of the catalyst of preparation, to wherein adding the phenol solution that contains about 9wt% acetone, and keep reaction temperature at about 70 ℃, increment flowing reactive still operate in 2.7mg raw material/mg dried resin/hour space velocity and the state of about 0.9 hour liquid residence time under.Take turns adding alternately and after reactant mixture shifted out, the composition in the reactor was near stable state about 40, therefrom sample analysis visible 4,4 '-isopropylidene bis-phenol (p, p-BPA) and 4, and 2 '-isopropylidene bis-phenol (o, p-BPA) and 8 kinds of other a small amount of components that form sometimes.Table 1 has been listed the p that generates, the percentage by weight of p-BPA and p, and p-BPA and o, the ratio of p-BPA (" pp/op ratio ") and total p, the p-BPA selectivity, it is defined as p, the weight fraction that p-BPA accounts in all detected products.
Show the preparation of 1.pp-BPA, use the phenol solution of 9% acetone, 70 ℃ were reacted l hour down, adopted the functionalized Rohm and Haas A131 resin of following promoter (1meq/g, 19% neutralization) catalysis.
| On average | On average | On average | Standard deviation | Standard deviation | Standard deviation | ||
| Promoter | pp/op | pp-BPA | pp-BPA | pp/op | pp-BPA | pp-BPA | |
| Ratio | Selectivity | wt％ | % output | Ratio | Selectivity | wt％ | |
| 2-(3 '-uncle's butylthio rosickyite base ethyl) pyridine | 46.37 | 95.75 | 24.80 | 70.1 | 1.66 | 0.01 | 0.92 |
| 2-(6 '-the own sulfenyl of uncle's butylthio) pyridine | 49.12 | 95.73 | 27.86 | 78.7 | 0.36 | 0.08 | 1.38 |
| 4-(6 '-the own sulfenyl ethyl of uncle's butylthio) pyridine | 48.59 | 95.73 | 29.94 | 84.6 | 1.58 | 0.08 | 5.21 |
| 2-(6 '-the own sulfenyl of uncle's butylthio) benzothiazole | 46.19 | 95.70 | 24.33 | 68.8 | 0.78 | 0.03 | 0.23 |
| 2-(4 '-uncle's butylthio butylthio) pyridine | 47.31 | 95.65 | 26.30 | 74.3 | 0.34 | 0.01 | 0.34 |
| 2-(5 '-uncle's butylthio penta sulfenyl) benzothiazole | 47.28 | 95.65 | 25.95 | 73.3 | 2.06 | 0.03 | 2.34 |
| 4-(4 '-uncle's butylthio butylthio ethyl) pyridine | 48.67 | 95.65 | 25.96 | 73.4 | 0.62 | 0.10 | 0.52 |
| 4-(5 '-uncle's butylthio penta sulfenyl ethyl) pyridine | 45.27 | 95.62 | 27.96 | 79.0 | 0.40 | 0.08 | 2.87 |
| 2-(5 '-uncle's butylthio penta sulfenyl) pyridine | 51.42 | 95.62 | 27.71 | 78.3 | 1.17 | 0.02 | 0.16 |
| 2-(3 '-uncle's butylthio rosickyite base) pyridine | 41.58 | 95.53 | 23.71 | 67.0 | 1.02 | 0.01 | 0.51 |
| 4-(3 '-uncle's butylthio rosickyite base ethyl) pyridine | 46.01 | 95.50 | 23.24 | 65.7 | 0.26 | 0.03 | 1.49 |
| 1-methyl-2-(3 '-uncle's butylthio rosickyite base) imidazoles | 41.85 | 95.42 | 21.99 | 62.2 | 0.86 | 0.03 | 0.47 |
| 4-(3 '-uncle's butylthio rosickyite base) pyridine | 39.18 | 95.39 | 21.34 | 60.3 | 0.18 | 0.05 | 0.14 |
| 2-(6 '-the own sulfenyl of uncle's butylthio) benzimidazole | 44.49 | 95.39 | 23.97 | 67.7 | 0.73 | 0.00 | 0.04 |
| 2-(4 '-uncle's butylthio butylthio) benzothiazole | 40.02 | 95.38 | 22.48 | 63.5 | 0.01 | 0.00 | 1.17 |
| 2-(5 '-uncle's butylthio penta sulfenyl) benzimidazole | 45.41 | 95.34 | 22.65 | 64.0 | 0.31 | 0.07 | 1.54 |
| 6-ethyoxyl-2-(3 '-uncle's butylthio rosickyite base) benzothiazole | 38.11 | 95.31 | 21.63 | 61.1 | 1.16 | 0.14 | 0.28 |
| 2-(4 '-uncle's butylthio butylthio) benzimidazole | 42.77 | 95.29 | 23.53 | 66.5 | 2.59 | 0.00 | 8.95 |
| 2-(3 '-uncle's butylthio rosickyite base) benzothiazole | 37.64 | 95.19 | 21.95 | 62.0 | 0.63 | 0.05 | 0.87 |
| 2-(3 '-uncle's butylthio rosickyite base) benzimidazole | 38.40 | 95.12 | 22.09 | 62.4 | 0.64 | 0.01 | 1.56 |
| The 4-tert-butyl group-sulphomethyl benzyl amine, carbon dioxide network and thing | 38.50 | 95.06 | 23.52 | 66.5 | 1.47 | 0.00 | 0.64 |
| 5-methyl-2-(3 '-uncle butylthio rosickyite base) benzimidazole hydrochloride | 37.37 | 95.05 | 22.17 | 62.7 | 2.52 | 0.09 | 0.23 |
| 4-pyridine radicals ethyl mercaptan | 33.82 | 94.98 | 22.64 | 64.0 | 0.26 | 0.14 | 1.39 |
| 2-(2 '-uncle's butylthio ethyl) pyridine | 32.07 | 94.85 | 26.89 | 76.0 | 0.53 | 0.11 | 0.30 |
| 5-sulfydryl amylamine hydrochloride | 38.10 | 94.82 | 27.18 | 76.8 | 0.55 | 0.52 | 0.16 |
| 1-(3 '-uncle's butylthio propyl group)-1,3-dihydro-2-benzimidazolone | 27.21 | 94.13 | 21.50 | 60.8 | 0.82 | 0.08 | 1.47 |
| The chlorination 4-tert-butyl group-sulphomethyl benzyl triethyl ammonium | 24.58 | 93.90 | 18.77 | 53.1 | 0.03 | 0.10 | 0.30 |
Sulfenyl: thio
Uncle's butylthio: tert-butylthio
Rosickyite base: propylthio
Own sulfenyl: hexylthio
Penta sulfenyl: pentylthio
According to the result in the table 1, obviously find the catalyst that makes by the promoter of enumerating in this method use table 1 effectively catalysis make pp-BPA by phenol and acetone.As a comparison, when Rohmand Haas A131 resin particle keyed jointing promoter not, when using by above-mentioned same condition, the pp-BPA that makes is 9.9wt%, and the pp selection rate is about 83.8%, and it is about 7.5 that pp/op leads.Use by above-mentioned same condition and work as Rohm andHaas A131 resin; when not having tert-butoxycarbonyl to carry out mercaptamine (cysteamine) promoter of sulphur protection; the pp-BPA that makes is 22.5wt%, and the pp selection rate is about 93.7%, and it is about 23.9 that pp/op leads.
More than the present invention is given an example and illustrates, but top description and example do not plan to be limited to given details, because can make amendment to the present invention and substitute at any way that does not break away from spirit of the present invention.Therefore, those of ordinary skills can use and be no more than routine test, provide the disclosure of invention is further revised and replaced, and believe that all such modifications and replacement are all in the spirit and scope of claims definition of the present invention.
Claims (83)
1, preparation catalysis is formed the method for the carbon monoxide-olefin polymeric of bis-phenol by aromatic hydroxy compound and the compound that contains carbonyl, described method comprises the then step on the solid acid component that contains functionalized protonic acid group of poly-sulphur mercaptan promoter component, described poly-sulphur mercaptan promoter component has structure (I)
R wherein
1Be to be selected from following functional group: the phosphorus functional group and the neutral amine of the ammonium functional group of positively charged, the guanidine functional group of positively charged, positively charged;
Wherein a is about 0 to about 11;
Wherein b is about 1 to about 11;
Wherein c is about 1 to about 11;
Wherein d is about 1 to about 5;
Wherein X connects functional group, is to be selected from a kind of in following: contain 1 the linear aliphatic chain of having an appointment to about 11 carbon atoms, contain at least 5 carbon atoms the aliphatic ring, contain at least 6 carbon atoms aromatic ring, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the heteroaromatic of at least 3 carbon atoms;
Wherein Y connects functional group, is to be selected from a kind of in following: contain 1 the linear aliphatic chain of having an appointment to about 11 carbon atoms, contain at least 5 carbon atoms the aliphatic ring, contain at least 6 carbon atoms aromatic ring, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the heteroaromatic of at least 3 carbon atoms;
R wherein
2Be to be selected from a kind of in following: hydrogen, secondary aliphatic functionality, uncle's aliphatic functionality, ester functional group, carbonate functionalities and the benzylic functionalities of following by benzyl Central Asia methine carbon atom.
2, according to the process of claim 1 wherein that described uncle's aliphatic functionality is to be selected from a kind of in following: branching aliphatic functionality or annular aliphatic functional group.
3, according to the process of claim 1 wherein described R
2Functional group is selected from a kind of in following: isopropyl functional group, isobutyl group functional group, t-butyl groups, tertiary pentyl functional group, cyclopenta functional group, benzylic functionalities, 4-mehtoxybenzyl functional group, 1-methylcyclohexyl functional group, cyclohexyl functional group.
4, according to the process of claim 1 wherein that described ester functional group is selected from a kind of in following: acetate functional group, propionic ester functional group and benzoic ether functional group.
5, according to the process of claim 1 wherein that described carbonate functionalities is to be selected from a kind of in following: alkyl carbonate functional group and aromatic carbonate functional group.
6, according to the process of claim 1 wherein that the bis-phenol that forms is 4,4 '-isopropylidene bis-phenol.
7, according to the process of claim 1 wherein that the compound that contains carbonyl is ketone or aldehyde.
8, according to the process of claim 1 wherein that aromatic hydroxy compound is that phenol, the compound that contains carbonyl are acetone.
9, according to the process of claim 1 wherein that then step is to finish in containing the aqueous solution of water.
10, be selected from least a in following according to the process of claim 1 wherein that described solid acid contains: polystyrene, zeolite and silica.
11, preparation catalysis is formed the method for the carbon monoxide-olefin polymeric of bis-phenol by aromatic hydroxy compound and the compound that contains carbonyl, described method comprises the then step on the polymer resin components that contains functionalized protonic acid group of poly-sulphur mercaptan promoter component, wherein said poly-sulphur mercaptan promoter component is to be selected from a kind of in following: functionalized pyridine mercaptan, functionalized benzimidazole mercaptan, functionalized benzothiazole mercaptan and functionalized imidazoles mercaptan.
12, according to the method for claim 11, wherein said functionalized pyridine mercaptan has structure (II):
Wherein e is about 0 to about 11;
Wherein f is about 1 to about 11;
Wherein g is about 1 to about 1;
Wherein h is about 1 to about 5;
Wherein X connects functional group, is to be selected from a kind of in following: contain 1 the linear aliphatic chain of having an appointment to about 11 carbon atoms, contain at least 5 carbon atoms the aliphatic ring, contain at least 6 carbon atoms aromatic ring, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the heteroaromatic of at least 3 carbon atoms;
Wherein Y connects functional group, is to be selected from a kind of in following: contain 1 the linear aliphatic chain of having an appointment to about 11 carbon atoms, contain at least 5 carbon atoms the aliphatic ring, contain at least 6 carbon atoms aromatic ring, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the heteroaromatic of at least 3 carbon atoms;
R wherein
3Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein at least one is selected from R
4, R
5, R
6, R
7And R
8, be { [(X)
eS]
f[(Y)
gS-R
3] chain, R
4, R
5, R
6, R
7And R
8In be not { [(X)
eS]
f[(Y)
gS-R
3] each of chain is to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the pyridine ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the pyridine ring by the adjacent ring substituting group.
13, according to the method for claim 11, wherein said functionalized benzimidazole mercaptan has structure (III):
Wherein i is about 0 to about 11;
Wherein j is about 1 to about 11;
Wherein k is about 1 to about 11;
R wherein
9Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
R wherein
10Be to be selected from a kind of in following: hydrogen, contain about 1 aliphatic carbonyl functional group, contain about 1 aliphatic functionality, contain aromatic series carbonyl functional group, contain aromatic series functional group at least about 6 carbon atoms at least about 7 carbon atoms to about 11 carbon atoms to about 11 carbon atoms;
R wherein
11, R
12, R
13And R
14In each be to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the benzimidazole aromatic hydrocarbon ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the benzimidazole aromatic hydrocarbon ring by the adjacent ring substituting group.
14, according to the method for claim 11, wherein said functionalized benzothiazole mercaptan has structure (IV):
Wherein l is about 0 to about 11;
Wherein m is about 1 to about 11;
Wherein n is about 1 to about 11;
R wherein
15Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
R wherein
16, R
17, R
18And R
19In each be to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the benzothiazole aromatic hydrocarbon ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the benzothiazole aromatic hydrocarbon ring by the adjacent ring substituting group.
15, according to the method for claim 11, wherein said functionalized imidazoles mercaptan has structure (V):
Wherein o is about 0 to about 11;
Wherein p is about 1 to about 11;
Wherein q is about 1 to about 11;
R wherein
20Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
R wherein
21Be to be selected from a kind of in following: hydrogen, contain about 1 aliphatic carbonyl functional group, contain about 1 aliphatic functionality, contain aromatic series carbonyl functional group, contain aromatic series functional group at least about 6 carbon atoms at least about 7 carbon atoms to about 11 carbon atoms to about 11 carbon atoms; With
R wherein
22And R
23In each be to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the imidazole ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the imidazole ring by the adjacent ring substituting group.
16, according to the method for claim 11, wherein the bis-phenol of Xing Chenging is 4,4 '-isopropylidene bis-phenol.
17, according to the method for claim 11, the compound that wherein contains carbonyl is ketone or aldehyde.
18, according to the method for claim 11, wherein aromatic hydroxy compound is a phenol, and the compound that contains carbonyl is an acetone.
19, according to the method for claim 11, wherein then step is to carry out in containing the aqueous solution of water.
20, according to the method for claim 11, wherein said fluoropolymer resin comprises and is selected from least a in following: polystyrene, zeolite and tripoli.
21, according to the method for claim 20, wherein said fluoropolymer resin also contains divinylbenzene.
22, according to the method for claim 21, wherein divinylbenzene accounts for fluoropolymer resin gross weight about 12%.
23, according to the method for claim 11, wherein said functionalized protonic acid group comprises and is selected from least a in following: sulfonic acid functional group, phosphoric acid functional group and carboxylic acid functional.
24, according to the method for claim 12, wherein connecting the X of functional group is the same with being connected the Y of functional group.
25, according to the method for claim 12, wherein X is-CH
2-Ji, e are 2, and f is 1, and Y is-CH
2-Ji, g are 3, R
4Be { [(X)
eS]
f[(Y)
gS-R
3] chain.
26, according to the method for claim 12, wherein X is-CH
2-Ji, e are 2, and f is 1, and Y is-CH
2-Ji, g are 3, R
5Be { [(X)
eS] [(Y)
gS-R
3] chain.
27, according to the method for claim 12, wherein X is-CH
2-Ji, e are 2, and f is 1, and Y is-CH
2-Ji, g are 3, R
6Be { [(X)
eS]
f[(Y)
gS-R
3] chain.
28, according to the method for claim 12, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
24Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein r is 3 or 6.
29, according to the method for claim 12, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
25Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein t is 3 or 6.
30, according to the method for claim 12, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
26Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein u is 3 or 6.
31, according to the method for claim 12, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
27Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein v is 3 or 6.
32, according to the method for claim 12, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
28Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein w is 3 or 6.
33, according to the method for claim 12, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
29Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein x is 3 or 6.
34, according to the method for claim 13, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
30Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms 11 that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom.
35, according to the method for claim 13, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, states promoter component and is:
R wherein
31Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom.
36, according to the method for claim 13, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
32Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom.
37, according to the method for claim 14, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
33Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein y is 3 or 6.
38, the method for preparing bis-phenol comprises the step that aromatic hydroxy compound and the compound that contains carbonyl are reacted when carbon monoxide-olefin polymeric exists, described catalyst comprises solid acid component and has the poly-sulphur mercaptan promoter of following structure (I)
R wherein
1Be to be selected from following functional group: the phosphorus functional group and the neutral amine of the ammonium functional group of positively charged, the guanidine functional group of positively charged, positively charged;
Wherein a is about 0 to about 11;
Wherein b is about 1 to about 11;
Wherein c is about 1 to about 11;
Wherein d is about 1 to about 5;
Wherein X connects functional group, is to be selected from a kind of in following: contain 1 the linear aliphatic chain of having an appointment to about 11 carbon atoms, contain at least 5 carbon atoms the aliphatic ring, contain at least 6 carbon atoms aromatic ring, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the heteroaromatic of at least 3 carbon atoms;
Wherein Y connects functional group, is to be selected from a kind of in following: contain 1 the linear aliphatic chain of having an appointment to about 11 carbon atoms, contain at least 5 carbon atoms the aliphatic ring, contain at least 6 carbon atoms aromatic ring, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the heteroaromatic of at least 3 carbon atoms;
R wherein
2Be to be selected from a kind of in following: hydrogen, secondary aliphatic functionality, uncle's aliphatic functionality, ester functional group, carbonate functionalities and the benzylic functionalities of following by benzyl Central Asia methine carbon atom.
39, according to the method for claim 38, wherein said uncle's aliphatic functionality is to be selected from a kind of in following: branching aliphatic functionality or annular aliphatic functional group.
40, according to the method for claim 38, wherein said R
2Be to be selected from a kind of in following: isopropyl functional group, isobutyl group functional group, t-butyl groups, tertiary pentyl functional group, cyclopenta functional group, benzylic functionalities, 4-mehtoxybenzyl functional group, 1-methylcyclohexyl functional group and cyclohexyl functional group.
41, according to the method for claim 38, wherein said ester functional group is selected from a kind of in following: acetate functional group, propionic ester functional group and benzoic ether functional group.
42, according to the method for claim 38, wherein said carbonate functionalities is to be selected from a kind of in following: alkyl carbonate functional group and aromatic carbonate functional group.
43, according to the method for claim 38, wherein the bis-phenol of Sheng Chenging is 4,4 '-isopropylidene bis-phenol.
44, according to the method for claim 38, wherein aromatic hydroxy compound is a phenol.
45, according to the method for claim 38, the compound that wherein contains carbonyl is aldehyde or ketone.
46, according to the method for claim 45, wherein ketone is acetone.
47, according to the method for claim 38, wherein said solid acid comprises and is selected from least a in following: polystyrene, zeolite, tripoli.
48, according to the method for claim 38, wherein said solid acid is the fluoropolymer resin of sulfonic acid functional.
49, according to the method for claim 48, wherein fluoropolymer resin also contains divinylbenzene.
50, according to the method for claim 49, wherein divinylbenzene accounts for about 12% of fluoropolymer resin gross weight.
51, according to the method for claim 38, wherein said solid acid component comprises and is selected from least a in following: sulfonic acid functional group, phosphoric acid functional group, carboxylic acid functional.
52, according to the method for claim 38, wherein connecting the X of functional group is the same with being connected the Y of functional group.
53, the method for preparing bis-phenol, comprise aromatic hydroxy compound and the compound that contains carbonyl are reacted in the presence of carbon monoxide-olefin polymeric, wherein said carbon monoxide-olefin polymeric comprises polymer resin components and the poly-sulphur mercaptan promoter component that contains functionalized protonic acid group, and wherein said poly-sulphur thiol component is to be selected from a kind of in following: functionalized pyridine mercaptan, functionalized benzimidazole mercaptan, functionalized benzothiazole mercaptan, functionalized imidazoles mercaptan.
54, according to the method for claim 53, wherein functionalized pyridine mercaptan has structure (II):
Wherein e is about 0 to about 11;
Wherein f is about 1 to about 11;
Wherein g is about 1 to about 11;
Wherein h is about 1 to about 5;
Wherein X connects functional group, is to be selected from a kind of in following: contain 1 the linear aliphatic chain of having an appointment to about 11 carbon atoms, contain at least 5 carbon atoms the aliphatic ring, contain at least 6 carbon atoms aromatic ring, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the heteroaromatic of at least 3 carbon atoms;
Wherein Y connects functional group, is to be selected from a kind of in following: contain 1 the linear aliphatic chain of having an appointment to about 11 carbon atoms, contain at least 5 carbon atoms the aliphatic ring, contain at least 6 carbon atoms aromatic ring, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the heteroaromatic of at least 3 carbon atoms;
R wherein
3Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein at least one is selected from R
4, R
5, R
6, R
7And R
8, be { [(X)
eS]
f[(Y)
gS-R
3] chain, R
4, R
5, R
6, R
7And R
8In be not { [(X)
eS]
f[(Y)
gS-R
3] each of chain is to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the pyridine ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the pyridine ring by the adjacent ring substituting group.
55, according to the method for claim 53, wherein functionalized benzimidazole mercaptan has structure (III):
Wherein i is about 0 to about 11;
Wherein j is about 1 to about 11;
Wherein k is about 1 to about 11;
R wherein
9Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
R wherein
10Be to be selected from a kind of in following: hydrogen, contain about 1 aliphatic carbonyl functional group, contain about 1 aliphatic functionality, contain aromatic series carbonyl functional group, contain aromatic series functional group at least about 6 carbon atoms at least about 7 carbon atoms to about 11 carbon atoms to about 11 carbon atoms;
R wherein
11, R
12, R
13And R
14In each be to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the benzimidazole aromatic hydrocarbon ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the benzimidazole aromatic hydrocarbon ring by the adjacent ring substituting group.
56, according to the method for claim 53, wherein said functionalized benzothiazole mercaptan has structure (IV):
Wherein l is about 0 to about 11;
Wherein m is about 1 to about 11;
Wherein n is about 1 to about 11;
R wherein
15Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
R wherein
16, R
17, R
18And R
19In each be to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the benzothiazole aromatic hydrocarbon ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the benzothiazole aromatic hydrocarbon ring by the adjacent ring substituting group.
57, according to the method for claim 53, wherein said functionalized imidazoles mercaptan has structure (V):
Wherein o is about 0 to about 11;
Wherein p is about 1 to about 11;
Wherein q is about 1 to about 11;
R wherein
20Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
R wherein
21Be to be selected from a kind of in following: hydrogen, contain about 1 aliphatic carbonyl functional group, contain about 1 aliphatic functionality, contain aromatic series carbonyl functional group, contain aromatic series functional group at least about 6 carbon atoms at least about 7 carbon atoms to about 11 carbon atoms to about 11 carbon atoms; With
R wherein
22And R
23In each be to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the imidazole ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the imidazole ring by the adjacent ring substituting group.
58, according to the method for claim 53, wherein the bis-phenol of Sheng Chenging is 4,4 '-isopropylidene bis-phenol.
59, according to the method for claim 53, wherein aromatic hydroxy compound is a phenol.
60, according to the method for claim 53, the compound that wherein contains carbonyl is aldehyde or ketone.
61, according to the method for claim 60, wherein ketone is acetone.
62, according to the method for claim 53, wherein said fluoropolymer resin comprises and is selected from least a in following: polystyrene, zeolite, tripoli.
63, according to the method for claim 62, wherein said fluoropolymer resin also contains divinylbenzene.
64, according to the method for claim 63, wherein divinylbenzene accounts for about 12% of fluoropolymer resin gross weight.
65, according to the method for claim 53, wherein said functionalized protonic acid group comprises and is selected from least a in following: sulfonic acid functional group, phosphoric acid functional group, carboxylic acid functional.
66, according to the method for claim 54, wherein connecting the X of functional group is the same with being connected the Y of functional group.
67, according to the method for claim 54, wherein X is-CH
2-Ji, e are 2, and f is 1, and Y is-CH
2-Ji, g are 3, R
4Be { [(X)
eS]
f[(Y)
gS-R
3] chain.
68, according to the method for claim 54, wherein X is-CH
2-Ji, e are 2, and f is 1, and Y is-CH
2-Ji, g are 3, R
5Be { [(X)
eS]
f[(Y)
gS-R
3] chain.
69, according to the method for claim 54, wherein X is-CH
2-Ji, e are 2, and f is 1, and Y is-CH
2-Ji, g are 3, R
6Be { [(X)
eS]
f[(Y)
gS-R
3] chain.
70, according to the method for claim 54, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
24Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein r is 3 or 6.
71, according to the method for claim 54, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
25Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein t is 3 or 6.
72, according to the method for claim 54, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
26Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein u is 3 or 6.
73, according to the method for claim 54, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
27Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein v is 3 or 6.
74, according to the method for claim 54, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
28Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein w is 3 or 6.
75, according to the method for claim 54, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
29Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein x is 3 or 6.
76, according to the method for claim 55, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
30Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom.
77, according to the method for claim 55, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
31Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom.
78, according to the method for claim 55, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
32Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom.
79, according to the method for claim 56, wherein bis-phenol is 4, and 4 '-isopropylidene bis-phenol, aromatic hydroxy compound are phenol, and the compound that contains carbonyl is an acetone, and described promoter component is:
R wherein
33Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein y is 3 or 6.
80, the pyridine compounds that has following array structure (II),
Wherein e is about 0 to about 11;
Wherein f is about 1 to about 11;
Wherein g is about 1 to about 11;
Wherein h is about 1 to about 5;
Wherein X connects functional group, is to be selected from a kind of in following: contain 1 the linear aliphatic chain of having an appointment to about 11 carbon atoms, contain at least 5 carbon atoms the aliphatic ring, contain at least 6 carbon atoms aromatic ring, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the heteroaromatic of at least 3 carbon atoms;
Wherein Y connects functional group, is to be selected from a kind of in following: contain 1 the linear aliphatic chain of having an appointment to about 11 carbon atoms, contain at least 5 carbon atoms the aliphatic ring, contain at least 6 carbon atoms aromatic ring, contain the aliphatic heterocycle of at least 3 carbon atoms and contain the heteroaromatic of at least 3 carbon atoms;
R wherein
3Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
Wherein at least one is selected from R
4, R
5, R
6, R
7And R
8, be { [(X)
eS]
f[(Y)
gS-R
3] chain, R
4, R
5, R
6, R
7And R
8In be not { [(X)
eS]
f[(Y)
gS-R
3] each of chain is to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the pyridine ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the pyridine ring by the adjacent ring substituting group.
81, the benzimidazole compound that has following array structure (III),
Wherein i is about 0 to about 11;
Wherein j is about 1 to about 11;
Wherein k is about 1 to about 11;
R wherein
9Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
R wherein
10Be to be selected from a kind of in following: hydrogen, contain about 1 aliphatic carbonyl functional group, contain about 1 aliphatic functionality, contain aromatic series carbonyl functional group, contain aromatic series functional group at least about 6 carbon atoms at least about 7 carbon atoms to about 11 carbon atoms to about 11 carbon atoms;
R wherein
11, R
12, R
13And R
14In each be to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the benzimidazole aromatic hydrocarbon ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the benzimidazole aromatic hydrocarbon ring by the adjacent ring substituting group.
82, the benzothiazole compound that has following array structure (IV),
Wherein l is about 0 to about 11;
Wherein m is about 1 to about 11;
Wherein n is about 1 to about 11;
R wherein
15Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
R wherein
16, R
17, R
18And R
19In each be to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the benzothiazole aromatic hydrocarbon ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the benzothiazole aromatic hydrocarbon ring by the adjacent ring substituting group.
83, the imidazolium compounds that has following array structure (V),
Wherein o is about 0 to about 11;
Wherein p is about 1 to about 11;
Wherein q is about 1 to about 11;
R wherein
20Be hydrogen or be selected from a kind of sulphur-protection functional group in following: the mesomethylene carbon atom on the benzyl of passing through that contain aliphatic functionality at least about 4 carbon atoms, contain the 1 ester functional group to about 11 carbon atoms that has an appointment, contain 1 carbonate functionalities to about 11 carbon atoms of having an appointment, contains at least about 7 carbon atoms is connected to benzylic functionalities on the terminal sulphur atom;
R wherein
21Be to be selected from a kind of in following: hydrogen, contain about 1 aliphatic carbonyl functional group, contain about 1 aliphatic functionality, contain aromatic series carbonyl functional group, contain aromatic series functional group at least about 6 carbon atoms at least about 7 carbon atoms to about 11 carbon atoms to about 11 carbon atoms; With
R wherein
22And R
23In each be to be selected from a kind of in following independently: hydrogen, fluorine, bromine, chlorine, iodine, vinyl, hydroxyl, contain about 1 alkoxy-functional to about 11 carbon atoms, contain aryloxy group functional group at least about 6 carbon atoms, contain about 1 aliphatic functionality to about 11 carbon atoms, contain aromatic series functional group at least about 6 carbon atoms, contain the alicyclic ring at least about 5 carbon atoms, described alicyclic ring is fused on the imidazole ring by the adjacent ring substituting group; Contain the ring at least about the aromatic ring family of 6 carbon atoms, described aromatic ring family ring is fused on the imidazole ring by the adjacent ring substituting group.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2003/006435 WO2004078345A1 (en) | 2003-03-03 | 2003-03-03 | Method for producing bisphenol catalysts and bisphenols |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1771087A true CN1771087A (en) | 2006-05-10 |
| CN100551532C CN100551532C (en) | 2009-10-21 |
Family
ID=32961104
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|---|---|---|---|
| CN03826406.4A Expired - Fee Related CN100551532C (en) | 2003-03-03 | 2003-03-03 | The method for preparing bis-phenol catalyst and bis-phenol |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1601460A1 (en) |
| JP (1) | JP2006513848A (en) |
| CN (1) | CN100551532C (en) |
| AU (1) | AU2003219982A1 (en) |
| WO (1) | WO2004078345A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109414687A (en) * | 2016-06-24 | 2019-03-01 | 沙特基础工业全球技术有限公司 | Crosslinked polystyrene catalyst, preparation method and its usage |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN108602057B (en) | 2015-12-09 | 2022-01-18 | Ptt全球化学公共有限公司 | Ion exchange resin for producing bisphenol |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3639663A (en) * | 1965-07-01 | 1972-02-01 | Monsanto Chemicals | Thioalkylthiobenzothiazoles |
| JPS5785335A (en) * | 1980-11-14 | 1982-05-28 | Mitsubishi Chem Ind Ltd | Production of bisphenol |
| US4609762A (en) * | 1984-01-30 | 1986-09-02 | Products Research & Chemical Corp. | Thioethers having a high sulfur content and method therefor |
| DE3573778D1 (en) * | 1984-06-29 | 1989-11-23 | Ciba Geigy Ag | Process for the preparation of glycidyl thioethers |
| EP0166696B1 (en) * | 1984-06-29 | 1989-07-19 | Ciba-Geigy Ag | Lubricant additives |
| US4820740A (en) * | 1986-10-30 | 1989-04-11 | Shell Oil Company | Process and catalyst for production of bisphenol-A |
| DE3640153A1 (en) * | 1986-11-25 | 1988-05-26 | Bayer Ag | CHLORINE-1,2,4-OXADIAZOLE |
| JPH02167268A (en) * | 1988-12-21 | 1990-06-27 | Meiji Seika Kaisha Ltd | Novel heterocyclic compound |
| IE903395A1 (en) * | 1989-09-26 | 1991-04-10 | Takeda Chemical Industries Ltd | Triazole compounds, their production and use |
| TW232013B (en) * | 1992-04-24 | 1994-10-11 | Takeda Pharm Industry Co Ltd | |
| US5414152A (en) * | 1994-05-10 | 1995-05-09 | General Electric Company | Method for extending the activity of acidic ion exchange catalysts |
| JP3834837B2 (en) * | 1995-06-01 | 2006-10-18 | 三菱化学株式会社 | Method for producing bisphenol A |
| JP3752780B2 (en) * | 1997-05-20 | 2006-03-08 | 三菱化学株式会社 | Ion exchange resin and method for producing bisphenol using the same |
| GB2327944B (en) * | 1997-08-06 | 2001-10-10 | Ciba Sc Holding Ag | Hetercyclic thioethers as additives for lubricants |
| JP3700361B2 (en) * | 1997-12-18 | 2005-09-28 | 三菱化学株式会社 | Ion exchange resin and method for producing bisphenols using the same as a catalyst |
| CN1195722C (en) * | 2000-01-07 | 2005-04-06 | 出光兴产株式会社 | Process for producing bisphenol A |
-
2003
- 2003-03-03 JP JP2004569165A patent/JP2006513848A/en active Pending
- 2003-03-03 EP EP03716269A patent/EP1601460A1/en not_active Ceased
- 2003-03-03 CN CN03826406.4A patent/CN100551532C/en not_active Expired - Fee Related
- 2003-03-03 AU AU2003219982A patent/AU2003219982A1/en not_active Abandoned
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN109414687A (en) * | 2016-06-24 | 2019-03-01 | 沙特基础工业全球技术有限公司 | Crosslinked polystyrene catalyst, preparation method and its usage |
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| Publication number | Publication date |
|---|---|
| JP2006513848A (en) | 2006-04-27 |
| AU2003219982A1 (en) | 2004-09-28 |
| EP1601460A1 (en) | 2005-12-07 |
| CN100551532C (en) | 2009-10-21 |
| WO2004078345A1 (en) | 2004-09-16 |
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