CN1235965A - 制备磺化联苯乙烯-联苯化合物的方法) - Google Patents
制备磺化联苯乙烯-联苯化合物的方法) Download PDFInfo
- Publication number
- CN1235965A CN1235965A CN99108021A CN99108021A CN1235965A CN 1235965 A CN1235965 A CN 1235965A CN 99108021 A CN99108021 A CN 99108021A CN 99108021 A CN99108021 A CN 99108021A CN 1235965 A CN1235965 A CN 1235965A
- Authority
- CN
- China
- Prior art keywords
- compound
- following formula
- alkyl
- definition
- represent
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 39
- 238000002360 preparation method Methods 0.000 title claims abstract description 14
- ZMLPKJYZRQZLDA-UHFFFAOYSA-N 1-(2-phenylethenyl)-4-[4-(2-phenylethenyl)phenyl]benzene Chemical group C=1C=CC=CC=1C=CC(C=C1)=CC=C1C(C=C1)=CC=C1C=CC1=CC=CC=C1 ZMLPKJYZRQZLDA-UHFFFAOYSA-N 0.000 title claims abstract description 13
- 150000001875 compounds Chemical class 0.000 claims abstract description 52
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 32
- 230000001476 alcoholic effect Effects 0.000 claims abstract description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 42
- 239000000203 mixture Substances 0.000 claims description 41
- -1 Phenyl Chemical group 0.000 claims description 29
- 238000005406 washing Methods 0.000 claims description 28
- 238000006243 chemical reaction Methods 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 16
- 239000002904 solvent Substances 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 14
- 150000002367 halogens Chemical class 0.000 claims description 14
- 150000002431 hydrogen Chemical class 0.000 claims description 14
- 239000004744 fabric Substances 0.000 claims description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 8
- 239000000975 dye Substances 0.000 claims description 8
- 239000011734 sodium Chemical group 0.000 claims description 8
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 229910052708 sodium Chemical group 0.000 claims description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 4
- 229910052784 alkaline earth metal Chemical group 0.000 claims description 4
- 150000001342 alkaline earth metals Chemical group 0.000 claims description 4
- 229910052728 basic metal Chemical group 0.000 claims description 4
- 150000003818 basic metals Chemical group 0.000 claims description 4
- 239000011591 potassium Chemical group 0.000 claims description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 3
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 3
- 230000007062 hydrolysis Effects 0.000 claims description 3
- 238000006460 hydrolysis reaction Methods 0.000 claims description 3
- 239000001103 potassium chloride Substances 0.000 claims description 3
- 235000011164 potassium chloride Nutrition 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 2
- NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical compound [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 claims description 2
- 229910000105 potassium hydride Inorganic materials 0.000 claims description 2
- 239000012312 sodium hydride Substances 0.000 claims description 2
- 229910000104 sodium hydride Inorganic materials 0.000 claims description 2
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 claims description 2
- 125000000068 chlorophenyl group Chemical group 0.000 claims 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 1
- 238000005282 brightening Methods 0.000 abstract description 10
- 239000003599 detergent Substances 0.000 abstract description 6
- 239000000123 paper Substances 0.000 abstract description 4
- 239000004753 textile Substances 0.000 abstract description 2
- 239000000010 aprotic solvent Substances 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 239000000243 solution Substances 0.000 description 17
- 239000007787 solid Substances 0.000 description 15
- 230000002087 whitening effect Effects 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 238000001035 drying Methods 0.000 description 8
- 239000000835 fiber Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 6
- 239000004280 Sodium formate Substances 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 150000002466 imines Chemical class 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 6
- 235000019254 sodium formate Nutrition 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 239000004305 biphenyl Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- LBJNMUFDOHXDFG-UHFFFAOYSA-N copper;hydrate Chemical compound O.[Cu].[Cu] LBJNMUFDOHXDFG-UHFFFAOYSA-N 0.000 description 4
- OMFXVFTZEKFJBZ-HJTSIMOOSA-N corticosterone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@H](CC4)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OMFXVFTZEKFJBZ-HJTSIMOOSA-N 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 4
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 4
- 238000005160 1H NMR spectroscopy Methods 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 238000004061 bleaching Methods 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 150000002148 esters Chemical group 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 229950000244 sulfanilic acid Drugs 0.000 description 3
- 238000006277 sulfonation reaction Methods 0.000 description 3
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 2
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
- RXGUIWHIADMCFC-UHFFFAOYSA-N 2-Methylpropyl 2-methylpropionate Chemical compound CC(C)COC(=O)C(C)C RXGUIWHIADMCFC-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- DPDMMXDBJGCCQC-UHFFFAOYSA-N [Na].[Cl] Chemical compound [Na].[Cl] DPDMMXDBJGCCQC-UHFFFAOYSA-N 0.000 description 2
- 150000004703 alkoxides Chemical class 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000007844 bleaching agent Substances 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 210000004209 hair Anatomy 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- UVEWQKMPXAHFST-UHFFFAOYSA-N n,1-diphenylmethanimine Chemical compound C=1C=CC=CC=1C=NC1=CC=CC=C1 UVEWQKMPXAHFST-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- RWMKSKOZLCXHOK-UHFFFAOYSA-M potassium;butanoate Chemical compound [K+].CCCC([O-])=O RWMKSKOZLCXHOK-UHFFFAOYSA-M 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- YKYONYBAUNKHLG-UHFFFAOYSA-N propyl acetate Chemical compound CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 210000002700 urine Anatomy 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
- RSEBUVRVKCANEP-UHFFFAOYSA-N 2-pyrroline Chemical compound C1CC=CN1 RSEBUVRVKCANEP-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- FEHLIYXNTWAEBQ-UHFFFAOYSA-N 4-(4-formylphenyl)benzaldehyde Chemical compound C1=CC(C=O)=CC=C1C1=CC=C(C=O)C=C1 FEHLIYXNTWAEBQ-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 241000208202 Linaceae Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 230000018199 S phase Effects 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZPFKRQXYKULZKP-UHFFFAOYSA-N butylidene Chemical group [CH2+]CC[CH-] ZPFKRQXYKULZKP-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229910001919 chlorite Inorganic materials 0.000 description 1
- 229910052619 chlorite group Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000019628 coolness Nutrition 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N ferric oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000009970 fire resistant effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- JISVIRFOSOKJIU-UHFFFAOYSA-N hexylidene Chemical group [CH2+]CCCC[CH-] JISVIRFOSOKJIU-UHFFFAOYSA-N 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-M isovalerate Chemical compound CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000005341 metaphosphate group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- CFHIDWOYWUOIHU-UHFFFAOYSA-N oxomethyl Chemical group O=[CH] CFHIDWOYWUOIHU-UHFFFAOYSA-N 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZVJHJDDKYZXRJI-UHFFFAOYSA-N pyrroline Natural products C1CC=NC1 ZVJHJDDKYZXRJI-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- JFLKFZNIIQFQBS-FNCQTZNRSA-N trans,trans-1,4-Diphenyl-1,3-butadiene Chemical group C=1C=CC=CC=1\C=C\C=C\C1=CC=CC=C1 JFLKFZNIIQFQBS-FNCQTZNRSA-N 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/46—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton having the sulfo groups bound to carbon atoms of non-condensed six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/32—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of salts of sulfonic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/02—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof
- C07C303/04—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups
- C07C303/06—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups by reaction with sulfuric acid or sulfur trioxide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/02—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof
- C07C303/22—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof from sulfonic acids, by reactions not involving the formation of sulfo or halosulfonyl groups; from sulfonic halides by reactions not involving the formation of halosulfonyl groups
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/60—Optical bleaching or brightening
- D06L4/614—Optical bleaching or brightening in aqueous solvents
- D06L4/621—Optical bleaching or brightening in aqueous solvents with anionic brighteners
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/30—Luminescent or fluorescent substances, e.g. for optical bleaching
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
本发明涉及在强碱存在下、在醇溶剂或双极性非质子传递溶剂中应用如右所示的式(2)化合物与式(3)或式(4)化合物反应制备如右所示的式(1)的磺化联苯乙烯-联苯化合物的方法以及新的式(3)或式(4)化合物和它们的制备方法,上式中的R1、R1A、M、R2、R3和R4的定义如说明书中所述。本发明的磺化联苯乙烯-联苯化合物可用作织物、洗涤剂和纸的荧光增白剂。
Description
本发明涉及一种新的制备磺化联苯乙烯-联苯化合物的方法,涉及新的磺化亚胺中间产物和一种制备所说的中间产物的方法。
以前已经公开了许多制备磺化联苯乙烯-联苯化合物的方法。例如US3984399公开了4,4’-双(二甲氧基膦酰基甲基)-联苯与苯甲醛-2-磺酸反应,而CH505036公开了磺化苯甲醛与联苯的双-氧化膦反应以及联苯-4,4’-二醛与相应的取代芳基氧化膦反应。US4231957进一步公开了两种不同的芳族醛与联苯的双-磷鎓盐的逐步反应,由此产生不对称的衍生物。
这些方法的成功与否,很大程度上取决于所需要的苯甲醛的可得性和在缩合所需反应条件下它们的稳定性。在某些情况下,已经发现所需要的苯甲醛可以仅以很低的产率得到,或者当它们的可得性是以工业规模需要时所需要的苯甲醛是不容易分离的。
令人惊奇的是,现在已经发现,很容易得到的磺化亚胺能很容易地与4,4’-双-(烷氧基膦酰基甲基)-联苯反应,以很好的产率和纯度得到磺化联苯乙烯-联苯化合物。
相应的是,本发明的主题是一种制备下式(1)的磺化联苯乙烯-联苯化合物的方法,(1)其中,R1代表氢、C1-C5烷基、C1-C5烷氧基或卤素,R1A代表氢、C1-C5烷基、C1-C5烷氧基或卤素,M代表氢、碱金属或碱土金属或铵,其特征在于在强碱的存在下,在醇溶剂或在双极性非质子传递溶剂中,下式(2)的化合物与下面的式子(3)或(4)的化合物反应,(2)其中,R2代表C1-C5烷基,其中,R3代表任意地被C1-4烷氧基、卤素或SO3M取代的苯基或C1-12烷基,R4代表C2-6亚烷基或亚苯基,M、R1和R1A的定义同上。
作为C1-C12烷基,它们可以是甲基、乙基、任何丙基、丁基、戊基、己基、庚基、辛基、壬基、癸基、十一烷基或十二烷基的异构体。C1-C5烷氧基可以是甲氧基、乙氧基、正或异丙氧基、正-、仲或叔丁氧基、正戊氧基、异戊氧基或仲戊氧基,卤素可以是氟、氯、溴或碘,优选氯。C2-6亚烷基可以是亚乙基、亚丙基、亚丁基、亚戊基或亚己基,优选亚乙基、亚丙基或亚丁基。当M代表碱金属或碱土金属时,它们优选是Li、Na或K或Ca或Mg,而当M代表铵时,它们可以是NH4、单-、二-、三-或四-甲铵、单-、二-、三-或四-乙铵、单-、二-、三-或四-正或异丙铵、单-、二-、三-或四-正、仲或叔丁铵、单-、二-或三乙醇胺、单-、二-或三-正或异丙醇胺、单-、二-或三-正、仲或叔丁醇胺、吗啉、哌啶翁或吡咯啉。
该方法特别适合于制备式(1)的化合物,其中R1和R1A都代表氢或氯,M代表H、K或Na,最优选是下式(5)的化合物,(5)其中M’代表钾或钠。
通过4,4’-双-氯甲基联苯与亚磷酸三烷基酯,优选亚磷酸三甲酯或亚磷酸三乙酯反应可以得到式(2)的双-膦酰基甲基化合物。
当在该方法中所用的溶剂是醇时,其优选是甲醇、乙醇、丙醇或丁醇,而作为双极性非质子传递溶剂,优选的是二甲基甲酰胺、二甲基乙酰胺、二甲亚砜或N-甲基哌啶或它们的混合物。
在该方法中所用的强碱可以是氢化钠或氢化钾、氢氧化钠或氢氧化钾、或C1-C5醇的钠盐或钾盐或它们的混合物,优选的是甲醇钠或叔丁醇钾的混合物。
实施该方法的温度可以在很宽的范围内变化,例如约20℃-120℃,但是优选约50℃-100℃。
第二方面,本发明涉及制备式(1)的磺化联苯乙烯联苯化合物或其混合物的的方法,特征在于水解一种或多种式(3)的化合物,得到一种或多种下式(6)的苯甲醛:(6)其中M和R1的定义同上,其是在在强碱存在下,在非质子传递溶剂中与式(2)的化合物反应。
在上述的方法中所用的非质子传递溶剂可以是芳族溶剂,例如苯、甲苯、二甲苯、氯代苯、或优选是环状或直链酰胺,例如N-甲基吡咯烷酮、二甲基甲酰胺、二乙基甲酰胺或二甲基乙酰胺,或亚砜例如二甲基亚砜。
合适的强碱是碱金属氢氧化物、酰胺和醇盐。特别合适的是锂、钠或钾的含有1-5个碳原子的醇盐。
一般的,反应温度可以在10℃-所用溶剂的沸点之间变化,虽然一般在30-60℃的温度范围内进行反应是有利的。
在式(3)的化合物的水解中所用的溶剂是酯、醚或水。合适的酯包括乙酸正丁酯、乙酸异丁酯、乙酸乙酯、异丁酸异丁酯、乙酸正丙酯和乙酸异丙酯。合适的醚包括异丙基醚、四氢呋喃、二噁烷和二乙醚。优选的溶剂是水。
所用的水解试剂包括硫酸或盐酸的稀释溶液。优选的水解试剂是式(3)的酸的稀释溶液:(3)其中R1和R3的定义同上。
进行水解的温度可以在约0℃-100℃的温度范围内变化,但是优选的是在约20℃-40℃的温度范围内变化。
特别重要的是通过上述方法生产的以下磺化联苯乙烯-联苯化合物、50%化合物A、25%化合物B和25%化合物C的混合物: 50%化合物A 25%化合物B 25%化合物C在第三方面中,本发明涉及下式(3)的新的亚胺:(3)其中R3的表示C1-C12烷基或下式的基团其中R5是氢、卤素或C1-C4烷氧基,R1和M的定义同上,它们的制备方法包括下式(7)的化合物与磺化剂反应:(7)其中R1是和R3的定义同上。
在另一个优选的实施方案中,式(3)的亚胺是其中R3是C1-C4烷基的那些化合物。
作为化合物(7)转化为化合物(3)和化合物(10)转化为化合物(4)的磺化剂,可以使用浓硫酸、氯代磺酸、三氧化硫、在溶剂中的三氧化硫、液体二氧化硫和发烟硫酸或它们的混合物,25%的发烟硫酸是特别优选的。
在溶解的或细分散的状态,通过本发明的方法制备的磺化联苯乙烯-联苯化合物显示或多或少的明显的荧光。因此,按照本发明可以把它们用于荧光增白的合成的或天然的有机物质。
可以提及的这样的物质的例子是(但不是要由下面的给出的例子来限制本发明的范围)由下面的有机物质得到的织物纤维,就这一点来说已考虑了它的荧光增白:(a)可以通过开环作为聚合产物得到的聚酰胺,例如聚己内酰胺类型的那些化合物;(b)基于能够进行缩合反应的双官能或多官能化合物,作为聚缩合产物得到的聚酰胺,例如六亚甲基二胺己二酸酯;和(c)动物或植物源的天然织物有机物质,例如基于纤维素或蛋白质的那些物质,例如棉或毛、亚麻或丝。
要被荧光增白的有机物质可在工艺的不同阶段进行增白,并且优选在成品织物下进行。它们可以是例如以丝绞品、织物单纤维、纱、绞合纱、非纺的、毡、织物纤维、织物组合物或针织纤维的形式。
对于处理纤维织物,上面定义的增白剂是特别重要的。织物基质的处理优选是在含水的介质中进行,在含水的介质中特定的荧光增白剂是以细分散的形式存在(悬浮液、所谓的微观分散液和在某些情况下的溶液)。在该处理的过程中,可以任意的加入分散剂、稳定剂、润湿剂和另外的辅助剂。
该处理通常在约20-140℃的温度,例如在浴的沸点或在其沸点区域(约90℃)下进行。按照本发明,对于制备纤维基质,也可以使用在有机溶剂中的溶液或乳液,如在叫做溶剂印染(浸轧焙固染色法和在染色机中浸染法)的印染中所用的那些。
本发明可以使用的荧光增白剂也可以例如以下面的使用形式使用:(a)与所谓的“载体”、润湿剂、软化剂、膨胀剂、抗氧化剂、光稳定剂、热稳定剂和化学漂白剂(亚氯酸盐漂白剂和漂白浴添加剂)的混合物;(b)与交联剂和处理剂(例如淀粉或合成处理剂)的混合物,和也可以与很多种纤维处理方法,特别是合成树脂处理(例如防皱处理例如“洗涤和磨损”、“永久压烫”和“非熨烫”)结合,也可以耐火燃处理、软化处理、抗污处理或抗静电处理或抗微生物处理;(c)作为各种皂和洗涤剂的添加剂;(d)与其它的具有荧光增白作用的物质结合。
如果该增白过程与纤维处理或处理方法结合,在很多情况下该结合处理方法借助相应的稳定制剂,能有利地起作用,该相应稳定制剂含有具有荧光增白作用的浓化合物以至于得到所需要的增白作用。
在某些情况下,通过后处理达到该增白剂的完整作用。这可以是例如化学处理(例如酸处理)、热处理(例如加热)或化学处理/热处理结合。
根据本发明,要用的荧光增白剂的量与要荧光增白的物质有关,其可以在很宽的范围内变化。用很少的量已达到明显的耐久的作用,在某些情况下,例如用0.03%重的量。但是,也可以使用直至约0.5%重的量。对实际中大多数有意义的情况,相对于要荧光增白的物质,优选的荧光增白剂量是0.05%-0.5%重。
荧光增白剂也特别适合用作洗涤浴的添加剂或加入到工业和家用洗涤剂中,并且它们可以以各种方式加入。合适的是它们以在水中或在有机溶剂中的溶液形式加入到洗涤浴中,或者也可以以细分散的状态作为水分散液或浆液的形式加入。有利的是它们或它们的组分加到处于任何制备工艺相态下的家用或工业洗涤剂中,例如加到在洗涤粉喷雾干燥之前或者在制备液体洗涤剂混合物的过程中的所谓的“浆液”中。这些化合物可以以在水中或在其它溶剂中的溶液或分散液的形式加入,并且也可以在无辅助剂下,以干燥的增白剂粉末形式加入。但是,它们也可以以溶解的或预分散的形式喷在成品洗涤剂上。
可以使用的洗涤剂是公知的洗涤剂物质的混合物,例如碎片和粉末形式的皂,合成产物,高级脂肪醇的磺酸半酯的水溶性盐、芳基磺酸,它们是由高级烷基取代的和/或被烷基多取代的,与平均高分子量的醇的羧酸酯,脂肪酸酰氨基烷基或氨基芳基-甘油磺酸酯,脂肪醇的磷酸酯等。可以使用的所谓的“助洗剂”是例如碱金属聚磷酸盐和碱金属聚偏磷酸盐,碱金属焦磷酸盐,羧甲基纤维素的碱金属盐和其它的“污垢再沉淀抑制剂”,也可以是碱金属硅酸盐,碱金属碳酸盐,碱金属硼酸盐,碱金属过硼酸盐,次氮基三乙酸,乙二胺四乙酸,和泡末稳定剂例如高级脂肪酸的烷醇酰胺。另外,该洗涤剂可以含有例如抗静电剂,富脂皮肤防护剂,例如羊毛酯,酶,抗微生物剂,香料和染料。
增白剂具有特殊的优越性,使得它们在存在活性氯供体例如次氯酸盐的情况下也是有效的,并且可以在含有非离子洗涤剂例如烷基酚聚乙二醇醚的洗涤浴中使用,基本上不损失效果。另外,在存在过硼酸盐或过酸和活化剂的情况下,例如四乙酰基甘尿或乙二胺四乙酸是新的在粉状洗涤剂和在洗涤浴中非常稳定的增白剂。
按照本发明,增白剂的加入量,相对于液体的重量或粉状备用的洗涤剂的重量,为0.005-2%或更多,优选0.03-0.5%。当它们用来洗涤用纤维素纤维、聚酰胺纤维、有高级光度的纤维素纤维、毛等制得的织物时,含有指定量的本发明的荧光增白剂的洗涤液提供在日光下很亮的外观。
洗涤处理例如按如下进行:在5-100℃,优选在25-100℃,在装有1-10克/公斤的含有助洗剂和相对洗涤剂重量的0.05-1%的所要求保护的增白剂的洗涤剂组合物的洗涤浴中处理所指定的织物1-30分钟。液体比可以是1∶3-1∶50。洗涤之后,把这些织物漂清并按常规的方法干燥。该洗涤浴可以含有作为漂白添加剂的0.2克/升的活性氯(例如以次氯酸盐的形式)或0.1-2克/升的过硼酸钠。
按照本发明的增白剂也可以与“载体”用于漂清浴中。为此,把该增白剂加入到软化漂清剂中或其它漂清剂中,该漂清剂含有作为“载体”的例如聚乙烯醇、淀粉、丙烯酸基的共聚物或甲醛/尿或乙烯-尿或丙烯-尿衍生物,其量为漂清剂0.005-5%或更多,优选0.2-2%。当使用量为每升漂清浴1-100ml,优选2-25ml时,含有本发明的增白剂的这种类型的漂清剂对很多种类型的处理织物提供光亮的漂白效果。
本发明的化合物另一种应用是在纸制造过程中在纸浆中或在施胶机中(其在英国专利说明书1,247,934中已经有介绍)或优选在涂胶组合物中用于纸的增白。这样使用某些联苯乙烯-联苯荧光增白剂的涂胶组合物已经在英国专利说明书2,277,749中很详细的作了介绍。当按照本发明的方法制备的增白剂用在这种要用它们增白的配方纸时显示非常高的白度。
用下面的实施例来说明本发明,除非另有说明,所有的份数和百分数都是按重量计。实施例1
把7.2g苯甲醛缩苯胺(Beilstein 12,第195页)分批加到64g25%的发烟硫酸中,由此其温度升到85℃。然后把反应物加热到150℃,并在该温度下再搅拌20分钟。然后把该液体反应混合物倒到950ml乙酸乙酯中,在室温下搅拌1小时,过滤并洗涤。在干燥器中干燥后,得到13.66g化合物(101),其是白色粉末,在296-298℃熔融分解。
分析C13H11NO6S2.0.75H2O
计算:C44.00%,H3.48%,N3.95%,S18.08%
实测:C44.02%,H3.52%,N3.69%,S17.65%
把4.72g双-亚苄基乙二胺(Beilstein7,第214页)加到50g25%的发烟硫酸中,把混合物加热到150℃,并在该温度下再搅拌45分钟。冷后却,把该混合物加到乙酸乙酯中,并按实施例1所述处理,得到11.2g化合物(102)。
分析C16H16N2O6S2.1.7H2SO4
计算:C34.12%,H3.47%,N4.97%,S21.00%
把4.43g化合物(101)和2.05g 4,4’-双-(二甲氧基膦甲基)-联苯溶解在50ml二甲亚砜中。加0.6g叔丁酸钾和8.3g 30%的甲醇的甲酸钠溶液后,在80℃加热该混合物45分钟,然后加400ml丙酮。过滤沉淀的固体,通过用甲醇/水处理除去磺胺酸。提纯之后得到2.2g化合物(103)。
分析C28H20Na2O6S2.2.5H2O
计算:C55.35%,H4.14%,N10.56%,S7.40%
实测:C55.40%,H4.10%,N10.42%,S7.16%实施例4
把3.55g化合物(102)和2.05g4,4’-双-(二甲氧基膦甲基)-联苯溶解在50ml二甲亚砜中。加0.6g叔丁酸钾和18.8g 30%的甲醇的甲酸钠溶液后,在80℃加热该混合物45分钟,然后加500ml丙酮。过滤沉淀的固体,干燥后得到2.28g化合物(103)。实施例5(104)
向7.42g磺胺酸钾盐(0.04285mol)和15ml水的溶液中加5.05g苯甲醛(0.04713mol)。搅拌该混合物并在20℃加热。2分钟后,白色固体沉淀,并且温度升到27℃。把反应物冷却到0℃,过滤、洗涤和干燥,得到11g(75%收率)的化合物(104)。由H-NMR谱证实其结构式。1H-NMR谱:δ(ppm):7.25(d),7.6(m),7.7(d),8.0(d),8.7(s),其比例是2∶3∶2∶2∶1。实施例6(101)
把2g(0.0066mol)化合物(104)和7g30%的发烟硫酸(0.0265mol)的混合物加热到130℃(浴温)并且搅拌3小时。向该反应溶液中加150ml乙酸乙酯。过滤沉淀的固体并洗涤,得到2.5g化合物(101)。实施例7(105)
向25%发烟硫酸(63g;0.197mol)中慢慢加入热的(80℃)液体亚苄基苯胺(55.4g,0.3mol),然后把66%的发烟硫酸的硫酸溶液(105.1g,0.867mol)慢慢地加到该混合物中(在加的过程中控制温度)。然后把该混合物在110℃搅拌6小时,然后冷却到室温,倒入水(300g)中。过滤磺胺酸,用水洗涤并干燥。然后用50%的氢氧化钠溶液中和母液和洗涤液(pH3)。蒸馏出水,把残余物倒入二甲基甲酰胺(250g)中。过滤硫酸钠并用二甲基甲酰胺洗涤。最后部分蒸馏该二甲基甲酰胺溶液,得到350g14.1%化合物(105)/二甲基甲酰胺溶液(收率79%)。实施例8(103)
在45℃30毫巴的压力下,向二苯基磷酸甲酯88%(22.6g,0.05mol)和化合物(105)在二甲基甲酰胺(260.3g 8.1%;0.102mol)的溶液的混合物中慢慢的加27g(0.2mol)30%甲醇的甲酸钠溶液。加完后,在45℃30毫巴的压力下,搅拌反应混合物3小时,然后用硫酸(0.55g,pH3)中和。蒸馏二甲基甲酰胺,把得到的固体倒入煮沸的蒸馏水(150g)中并搅拌20分钟。在压力下过滤固体,然后用蒸馏水(150g)洗涤并且再过滤。最后干燥固体12小时(100℃,30毫巴),得到浅黄色化合物(103)(27.2g,纯度72%)(收率70%)。实施例9(103)
向4.43g(0.012ml)化合物(101)中加37%的1.2g盐酸(0.012mol)。向该混合物中加2.26g二苯基磷酸甲酯88%(0.005mol)和50ml二甲基甲酰胺。把该混合物中慢慢的加到8.3g(0.046mol)的30%甲醇的甲酸钠溶液中。加完后,在80℃30毫巴的压力下搅拌反应混合物3小时。在该过程中沉淀黄色固体。在25℃冷却之后过滤固体,然后用5ml二甲基甲酰胺洗涤二次,然后用10ml丙酮洗涤。最后干燥该化合物(103)12小时(80℃,30毫巴),得到浅黄色固体(2.0g;0.036mol),纯度95%(收率76%)。实施例10
在45℃30毫巴的压力下,向二苯基磷酸甲酯88%(17.5g,0.039mol)和4.5%的邻甲酰基磺酸钠盐(251.3g;0.0485ml)在二甲基甲酰胺中的溶液的混合物中慢慢的(5-10分钟)加8g(0.06mol)的30%甲醇的甲酸钠溶液。加完后,在45℃30毫巴的压力下搅拌该反应混合物2小时,然后在45℃在氮气下把化合物(105)/二甲基甲酰胺(11.85g,79.9%;0.044ml)加到该混合物中。在45℃30毫巴的压力下,向该得到的混合物中加8g(0.06mol)的30%甲醇的甲酸钠溶液。然后在45℃30毫巴的压力下搅拌该反应混合物5小时,并用甲酸100%(2ml,pH7)中和。蒸馏二甲基甲酰胺(最高100℃),然后把得到的固体倒入煮沸的蒸馏水(500g)中,在90℃搅拌15分钟。然后在90℃慢慢加55g氯化钠,在3个小时内慢慢的把该反应混合物冷却到25℃。在35℃把另外一部分55g氯化钠加完之后,在压力下过滤形成的固体,然后用150g氯化钠溶液(20%的水溶液)洗涤。最后干燥该固体12小时(80℃,30毫巴),得到浅黄色固体(25g;纯度76%)(收率85%)。HPLC分析显示约50%化合物A,25%化合物B和25%化合物C的混合物。
Claims (16)
2.根据权利要求1的方法,其中R1和R1A都表示氢或氯,M表示氢,钾或钠。
3.根据权利要求1的方法,其中R2代表甲基或乙基,R3代表苯基,氯代苯基或C1-C6烷基或C2-4亚烷基。
4.根据权利要求1的方法,其中溶剂是C1-4醇、二甲基甲酰胺、二甲基乙酰胺、二甲亚砜或N-甲基比咯烷酮或它们的混合物。
5.根据权利要求1的方法,其中强碱是氢化钠或氢化钾、氢氧化钠或氢氧化钾或C1-5醇的钠盐或钾盐或它们的混合物。
6.根据权利要求1的方法,其中反应是在约20-120℃的温度下进行。
10.根据权利要求9的下式(8)的化合物(8)其中R3表示C1-C12烷基或下式的基团(9):(9)其中R5是氢、卤素或C1-C4烷氧基,M和R1的定义同上。
11.根据权利要求9的化合物,其中R3是C1-C4烷基。
12.一种制备权利要求8的化合物的方法,其包括下式(6)的化合物与磺化剂反应,(6)其中R1和R3的定义同权利要求1。
14.一种制备权利要求13的化合物的方法,其包括下式(7)的化合物与磺化剂反应,(7)其中R1、R1A和R4的定义同权利要求1。
15.根据权利要求12或14的方法,其中磺化剂是浓硫酸、氯磺酸或发烟硫酸。
16.权利要求1-7的任一项的化合物和/或组合物作为织物、洗涤剂和纸的荧光增白剂的应用。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP98810432.9 | 1998-05-13 | ||
EP98810432 | 1998-05-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN1235965A true CN1235965A (zh) | 1999-11-24 |
Family
ID=8236081
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN99108021A Pending CN1235965A (zh) | 1998-05-13 | 1999-05-12 | 制备磺化联苯乙烯-联苯化合物的方法) |
Country Status (7)
Country | Link |
---|---|
US (1) | US6096919A (zh) |
JP (1) | JP2000026399A (zh) |
KR (1) | KR19990088223A (zh) |
CN (1) | CN1235965A (zh) |
BR (1) | BR9902074A (zh) |
DE (1) | DE69906181D1 (zh) |
IL (1) | IL129888A0 (zh) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002097193A1 (en) * | 2001-05-29 | 2002-12-05 | Ciba Specialty Chemicals Holding Inc. | A composition for the fluorescent whitening of paper |
US20070027252A1 (en) * | 2003-09-26 | 2007-02-01 | Ciba Specialty Chemicals Holding Inc. | Process for improving color of polycondensates |
MX2011008656A (es) | 2009-03-06 | 2011-09-06 | Huntsman Adv Mat Switzerland | Metodos de decoloracion-blanqueo enzimatico de textiles. |
CN102911509A (zh) * | 2012-10-26 | 2013-02-06 | 山西青山化工有限公司 | 一种二苯乙烯基联苯型荧光增白剂的环保制备方法 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH554848A (de) * | 1967-10-03 | 1974-10-15 | Ciba Geigy Ag | Verfahren zur herstellung neuer stilben-derivate. |
CH559757A5 (zh) * | 1971-09-01 | 1975-03-14 | Ciba Geigy Ag | |
DE2525683A1 (de) * | 1974-06-12 | 1976-01-02 | Ciba Geigy Ag | Sulfogruppenhaltige heterocyclen |
CH619336B (de) * | 1975-11-24 | Ciba Geigy Ag | Verwendung von distyrylbenzol- bzw. -diphenylverbindungen als optische aufhellmittel. | |
US4231957A (en) * | 1977-11-04 | 1980-11-04 | Ciba-Geigy Corporation | Phosphonium compounds, a process for their preparation and a process for the preparation of asymmetrically substituted stilbene fluorescent brightening agents |
TW229199B (zh) * | 1992-09-03 | 1994-09-01 | Ciba Geigy | |
GB2277749B (en) * | 1993-05-08 | 1996-12-04 | Ciba Geigy Ag | Fluorescent whitening of paper |
GB9422280D0 (en) * | 1994-11-04 | 1994-12-21 | Ciba Geigy Ag | Fluorescent whitening agent formulation |
-
1999
- 1999-05-04 DE DE69906181T patent/DE69906181D1/de not_active Expired - Lifetime
- 1999-05-10 US US09/309,232 patent/US6096919A/en not_active Expired - Fee Related
- 1999-05-11 JP JP11129422A patent/JP2000026399A/ja active Pending
- 1999-05-11 IL IL12988899A patent/IL129888A0/xx unknown
- 1999-05-12 KR KR1019990016943A patent/KR19990088223A/ko not_active Application Discontinuation
- 1999-05-12 BR BR9902074-2A patent/BR9902074A/pt not_active IP Right Cessation
- 1999-05-12 CN CN99108021A patent/CN1235965A/zh active Pending
Also Published As
Publication number | Publication date |
---|---|
KR19990088223A (ko) | 1999-12-27 |
DE69906181D1 (de) | 2003-04-30 |
IL129888A0 (en) | 2000-02-29 |
US6096919A (en) | 2000-08-01 |
JP2000026399A (ja) | 2000-01-25 |
BR9902074A (pt) | 2000-02-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE602005005702T2 (de) | Wäschebehandlungsmittel | |
CN1137107C (zh) | 茋化合物的制备方法 | |
BRPI0616917A2 (pt) | uso de uma composição | |
US2930760A (en) | Laundering compositions | |
AU618135B2 (en) | Bleaching and detergent compositions | |
DE2157785A1 (de) | Verfahren und mittel zum waschen und weichmachen von textilien | |
DE1924300B2 (de) | Wasch-, bleich- und reinigungsmittel | |
CN1235965A (zh) | 制备磺化联苯乙烯-联苯化合物的方法) | |
EP0131137B1 (de) | Wasch- und Reinigungsmittel mit einem Gehalt an Acylcyanamidsalzen | |
DE2165900A1 (de) | Waschmittel mit einem gehalt an vergrauungsverhuetenden zusaetzen | |
CA1094262A (en) | Brightening compositions | |
US3575866A (en) | New brighteners,compositions thereof and processes for using same | |
CN1215046A (zh) | 磺化二苯乙烯基-联苯化合物 | |
EP0957085B1 (en) | A process for the preparation of sulphonated distyryl-biphenyl compounds | |
US3728275A (en) | Preparations containing concentrated aqueous asymmetrically substituted bis-triazinylaminostilbenes and the use of the preparations for optical brightening | |
CN1308295C (zh) | 磺化联苯乙烯-联苯化合物的制备方法 | |
US3872114A (en) | Benzofurane derivatives, process for their manufacture and their use as optical brighteners | |
US3415752A (en) | Detergent compositions | |
DE2165834A1 (de) | Waschmittel mit einem gehalt an vergrauungsverhuetenden zusaaetzen | |
US3583925A (en) | Washing agents | |
US5434275A (en) | Dibenzofuranylbiphenyls | |
Findley | Whitener selection for today’s detergents | |
DE2165835A1 (de) | Waschmittel mit einem gehalt an vergrauungsverhuetenden zusaetzen | |
DE2213557A1 (de) | Verfahren und mittel zum waschen und weichmachen von textilien | |
MXPA99004355A (en) | A process for the preparation of diestiril-bifenyl sulphone compounds |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |