CN102408430B - 取代四苯基双铁卟啉的合成工艺与专用设备 - Google Patents
取代四苯基双铁卟啉的合成工艺与专用设备 Download PDFInfo
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- CN102408430B CN102408430B CN 201110263275 CN201110263275A CN102408430B CN 102408430 B CN102408430 B CN 102408430B CN 201110263275 CN201110263275 CN 201110263275 CN 201110263275 A CN201110263275 A CN 201110263275A CN 102408430 B CN102408430 B CN 102408430B
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- iron
- tetraphenyl
- porphyrins
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- 238000000034 method Methods 0.000 title claims abstract description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 30
- 239000007787 solid Substances 0.000 claims abstract description 23
- 239000003960 organic solvent Substances 0.000 claims abstract description 17
- 238000002425 crystallisation Methods 0.000 claims abstract description 12
- 238000011084 recovery Methods 0.000 claims abstract description 12
- 238000010992 reflux Methods 0.000 claims abstract description 12
- YNHJECZULSZAQK-UHFFFAOYSA-N tetraphenylporphyrin Chemical class C1=CC(C(=C2C=CC(N2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3N2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 YNHJECZULSZAQK-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000010438 heat treatment Methods 0.000 claims abstract description 9
- 230000008025 crystallization Effects 0.000 claims abstract description 4
- 238000006471 dimerization reaction Methods 0.000 claims abstract description 3
- 238000000746 purification Methods 0.000 claims abstract description 3
- JQRLYSGCPHSLJI-UHFFFAOYSA-N [Fe].N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 Chemical class [Fe].N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 JQRLYSGCPHSLJI-UHFFFAOYSA-N 0.000 claims description 52
- 238000006243 chemical reaction Methods 0.000 claims description 25
- 239000002904 solvent Substances 0.000 claims description 24
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 18
- 239000000706 filtrate Substances 0.000 claims description 15
- 238000001465 metallisation Methods 0.000 claims description 14
- 238000000967 suction filtration Methods 0.000 claims description 14
- 239000013078 crystal Substances 0.000 claims description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 12
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 12
- 238000001816 cooling Methods 0.000 claims description 9
- 230000018044 dehydration Effects 0.000 claims description 9
- 238000006297 dehydration reaction Methods 0.000 claims description 9
- 239000002699 waste material Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 150000002500 ions Chemical class 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 229920005989 resin Polymers 0.000 claims description 8
- 238000005406 washing Methods 0.000 claims description 8
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- 235000019260 propionic acid Nutrition 0.000 claims description 6
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 6
- 238000003786 synthesis reaction Methods 0.000 claims description 6
- -1 Hydrogen Chemical class 0.000 claims description 3
- 238000005086 pumping Methods 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 claims description 2
- 239000011790 ferrous sulphate Substances 0.000 claims description 2
- 235000003891 ferrous sulphate Nutrition 0.000 claims description 2
- 235000011194 food seasoning agent Nutrition 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical group Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 claims description 2
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims description 2
- 229910000359 iron(II) sulfate Inorganic materials 0.000 claims description 2
- LNOZJRCUHSPCDZ-UHFFFAOYSA-L iron(ii) acetate Chemical compound [Fe+2].CC([O-])=O.CC([O-])=O LNOZJRCUHSPCDZ-UHFFFAOYSA-L 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000012046 mixed solvent Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 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
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- 239000011368 organic material Substances 0.000 abstract 1
- 238000004821 distillation Methods 0.000 description 14
- 238000004519 manufacturing process Methods 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 description 4
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 238000004440 column chromatography Methods 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 3
- 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 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000007810 chemical reaction solvent Substances 0.000 description 2
- 229960001701 chloroform Drugs 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000009776 industrial production Methods 0.000 description 2
- 239000003456 ion exchange resin Substances 0.000 description 2
- 229920003303 ion-exchange polymer Polymers 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- BNUNBUAPWCPDSO-UHFFFAOYSA-N C1=CC([N+](=O)[O-])=CC=C1C1=CC2=CC([N]3)=CC=C3C=C(C=C3)NC3=CC([N]3)=CC=C3C=C1N2 Chemical class C1=CC([N+](=O)[O-])=CC=C1C1=CC2=CC([N]3)=CC=C3C=C(C=C3)NC3=CC([N]3)=CC=C3C=C1N2 BNUNBUAPWCPDSO-UHFFFAOYSA-N 0.000 description 1
- LEZRPXHDGLLVQS-UHFFFAOYSA-N COC1=CC=CC(C=2C3=CC4=CC=C([N]4)C=C4C=CC(N4)=CC4=CC=C([N]4)C=C(N3)C=2)=C1 Chemical class COC1=CC=CC(C=2C3=CC4=CC=C([N]4)C=C4C=CC(N4)=CC4=CC=C([N]4)C=C(N3)C=2)=C1 LEZRPXHDGLLVQS-UHFFFAOYSA-N 0.000 description 1
- GWEDZEGGJIRIKE-UHFFFAOYSA-N N1C2=CC([N]3)=CC=C3C=C(N3)C=CC3=CC([N]3)=CC=C3C=C1C(O)=C2C1=CC=CC=C1 Chemical class N1C2=CC([N]3)=CC=C3C=C(N3)C=CC3=CC([N]3)=CC=C3C=C1C(O)=C2C1=CC=CC=C1 GWEDZEGGJIRIKE-UHFFFAOYSA-N 0.000 description 1
- MPFSYDZCEKIPHH-UHFFFAOYSA-N NCC=1C(=C2NC=1C=C1C=CC(=N1)C=C1C=CC(N1)=CC=1C=CC(N=1)=C2)C1=CC=CC=C1 Chemical class NCC=1C(=C2NC=1C=C1C=CC(=N1)C=C1C=CC(N1)=CC=1C=CC(N=1)=C2)C1=CC=CC=C1 MPFSYDZCEKIPHH-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
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Families Citing this family (5)
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CN103880851B (zh) * | 2014-03-11 | 2016-03-02 | 沅江华龙催化科技有限公司 | 四芳基金属卟啉的连续生产工艺 |
CN103819480B (zh) * | 2014-03-11 | 2015-11-11 | 沅江华龙催化科技有限公司 | 四芳基双金属卟啉的连续生产工艺 |
CN105646505B (zh) * | 2016-01-15 | 2018-08-28 | 唐江涛 | 一种μ-氧代四苯基双金属卟啉的连续制备方法 |
CN108346807A (zh) * | 2018-02-08 | 2018-07-31 | 张树雄 | 气体扩散电极、催化剂、制备方法及催化层喷剂制备方法 |
CN109126877A (zh) * | 2018-09-20 | 2019-01-04 | 西北师范大学 | 一种铁(iii)四羧基苯基卟啉植入金属有机框架的制备和应用 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994019352A1 (de) * | 1993-02-17 | 1994-09-01 | Institut für Diagnostikforschung GmbH an der Freien Universität Berlin | Meso-tetraphenylporphyrin-komplexverbindungen, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische mittel |
CN1544435A (zh) * | 2003-11-21 | 2004-11-10 | 湖南大学 | 一种金属卟啉的合成方法 |
WO2006025859A2 (en) * | 2004-02-17 | 2006-03-09 | Johnson Thomas E | Methods, compositions, and apparatuses for forming macrocyclic compounds |
CN101225086A (zh) * | 2008-02-01 | 2008-07-23 | 北京工业大学 | 一种μ-氧代双核铁卟啉的合成方法 |
-
2011
- 2011-09-07 CN CN 201110263275 patent/CN102408430B/zh active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994019352A1 (de) * | 1993-02-17 | 1994-09-01 | Institut für Diagnostikforschung GmbH an der Freien Universität Berlin | Meso-tetraphenylporphyrin-komplexverbindungen, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische mittel |
CN1544435A (zh) * | 2003-11-21 | 2004-11-10 | 湖南大学 | 一种金属卟啉的合成方法 |
WO2006025859A2 (en) * | 2004-02-17 | 2006-03-09 | Johnson Thomas E | Methods, compositions, and apparatuses for forming macrocyclic compounds |
CN101225086A (zh) * | 2008-02-01 | 2008-07-23 | 北京工业大学 | 一种μ-氧代双核铁卟啉的合成方法 |
Non-Patent Citations (5)
Title |
---|
兽药》.化学工业出版社,1996,第1卷443-444. |
农药• |
复混肥料• |
潘长华主编.实用小化工生产大全 无机化工产品.《实用小化工生产大全 无机化工产品• |
潘长华主编.实用小化工生产大全 无机化工产品.《实用小化工生产大全 无机化工产品•复混肥料•农药•兽药》.化学工业出版社,1996,第1卷443-444. * |
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