CN102304071A - 二步法合成4.4-二氯二苯砜的方法 - Google Patents
二步法合成4.4-二氯二苯砜的方法 Download PDFInfo
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- CN102304071A CN102304071A CN201110245933A CN201110245933A CN102304071A CN 102304071 A CN102304071 A CN 102304071A CN 201110245933 A CN201110245933 A CN 201110245933A CN 201110245933 A CN201110245933 A CN 201110245933A CN 102304071 A CN102304071 A CN 102304071A
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- acid
- chlorobenzene
- dichlorodiphenyl sulfone
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- sulfuric acid
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- 238000000034 method Methods 0.000 title claims abstract description 21
- 230000002194 synthesizing effect Effects 0.000 title abstract 3
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims abstract description 22
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000006243 chemical reaction Methods 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 7
- 239000002253 acid Substances 0.000 claims abstract description 6
- 238000003756 stirring Methods 0.000 claims abstract description 6
- RJWBTWIBUIGANW-UHFFFAOYSA-N 4-chlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Cl)C=C1 RJWBTWIBUIGANW-UHFFFAOYSA-N 0.000 claims abstract description 4
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims abstract description 4
- 238000006482 condensation reaction Methods 0.000 claims abstract description 4
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 6
- 239000000047 product Substances 0.000 abstract description 5
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000006227 byproduct Substances 0.000 abstract description 2
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 abstract 2
- MNURPFVONZPVLA-UHFFFAOYSA-N 2-chlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1Cl MNURPFVONZPVLA-UHFFFAOYSA-N 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 abstract 1
- 229940098779 methanesulfonic acid Drugs 0.000 abstract 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 abstract 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- 239000004695 Polyether sulfone Substances 0.000 description 2
- 229920006351 engineering plastic Polymers 0.000 description 2
- 229920002492 poly(sulfone) Polymers 0.000 description 2
- 229920006393 polyether sulfone Polymers 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 2
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
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- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012847 fine chemical Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
一种二步法合成4.4-二氯二苯砜的方法,包括以下步骤:(1)对氯苯磺酸的制备——反应锅内加入质量浓度为98%浓硫酸及三氧化硫质量浓度为20%的发烟硫酸,搅拌15min,逐渐加入干燥的氯苯,在95-100℃搅拌反应5h,其中:浓硫酸与发烟硫酸的体积比为3:1;(2)4.4-二氯二苯砜的合成——以复合酸为催化剂,在40-60摄氏度下滴加氯苯,促使对氯苯磺酸与氯苯发生4-6小时的缩合反应,生成4.4-二氯二苯砜;所述复合酸由甲基磺酸以及五氧化二磷组成。由此可知,本发明采用两步法制备4.4-二氯二苯砜,可以降低整个反应的温度,从而减少反应过程中副产物的产生,提高产品的转化率。
Description
技术领域
本发明涉及一种4.4-二氯二苯砜的制备方法。
背景技术
4.4–二氯二苯砜,简称DDS,为白色晶体,可升华,易溶于苯、氯苯、DMF等有机溶剂;微溶于乙醇、甲醇;不溶于水。其闪点为233℃,沸点则为397℃。
4.4–二氯二苯砜在工程塑料和精细化工领域有着广泛的用途,是制备聚砜、聚醚砜等工程塑料的主要原料,也是医药、染料、农药的中间体。
目前,常用的4.4–二氯二苯砜的合成方法有:氯磺酸法、硫酸法以及三氧化硫法;其中,氯磺酸法制备4.4–二氯二苯砜的生产成本高,三废严重,且产品质量比较差,很难达到聚砜及聚醚砜生产所规定的质量要求;硫酸法反应温度高,反应时间长,对设备腐蚀严重,产品质量差,收率低;三氧化硫法整个工艺路线长,付克反应温度高,反应时间长,精制工艺路线复杂。
发明内容
本发明针对现有技术的不足,提供一种二步法合成4.4-二氯二苯砜的方法,其先合成对氯苯磺酸,然后再与氯苯在复合酸催化剂的作用下发生缩合反应,生成4.4-二氯二苯砜粗品,经分离处理后,即可得到4.4-二氯二苯砜,其得率较高,产品品质也很好。
为实现以上的技术目的,本发明将采取以下的技术方案:
一种二步法合成4.4-二氯二苯砜的方法,包括以下步骤:(1)对氯苯磺酸的制备——反应锅内加入质量浓度为98%浓硫酸及三氧化硫质量浓度为20%的发烟硫酸,搅拌15min,逐渐加入干燥的氯苯,在95-100℃搅拌反应5h,其中:浓硫酸与发烟硫酸的体积比为3:1;(2)4.4-二氯二苯砜的合成——以复合酸为催化剂,在40-60摄氏度下滴加氯苯,促使对氯苯磺酸与氯苯发生4-6小时的缩合反应,生成4.4-二氯二苯砜;所述复合酸由甲基磺酸以及五氧化二磷组成。
根据以上的技术方案,可以实现以下的有益效果:
本发明采用两步法制备4.4-二氯二苯砜,可以降低整个反应的温度,从而减少反应过程中副产物的产生,提高产品的转化率。
Claims (1)
1.一种二步法合成4.4-二氯二苯砜的方法,其特征在于,(1)对氯苯磺酸的制备——反应锅内加入质量浓度为98%浓硫酸及三氧化硫质量浓度为20%的发烟硫酸,搅拌15min,逐渐加入干燥的氯苯,在95-100℃搅拌反应5h,其中:浓硫酸与发烟硫酸的体积比为3:1;(2)4.4-二氯二苯砜的合成——以复合酸为催化剂,在40-60摄氏度下滴加氯苯,促使对氯苯磺酸与氯苯发生4-6小时的缩合反应,生成4.4-二氯二苯砜;所述复合酸由甲基磺酸以及五氧化二磷组成。
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| CN201110245933A CN102304071A (zh) | 2011-08-25 | 2011-08-25 | 二步法合成4.4-二氯二苯砜的方法 |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012143279A1 (en) * | 2011-04-18 | 2012-10-26 | Solvay Specialty Polymers Usa, Llc | Process for the manufacture of dihalodiphenylsulfones starting from organic acids |
| US9394248B2 (en) | 2011-04-18 | 2016-07-19 | Solvay Specialty Polymers Usa, Llc | Process for the manufacture of dihalodiphenylsulfones |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0062736A1 (en) * | 1979-06-15 | 1982-10-20 | Amoco Corporation | Process for preparing 4-4'-dichlorodiphenyl sulphone |
| US4822916A (en) * | 1987-09-21 | 1989-04-18 | Akzo America Inc. | Preparation of diaryl sulfones |
| EP0381045A2 (de) * | 1989-02-01 | 1990-08-08 | BASF Aktiengesellschaft | Verfahren zur Herstellung von Bis-(4-chlorphenyl)-sulfon |
| US4983773A (en) * | 1988-10-19 | 1991-01-08 | Basf Aktiengesellschaft | Preparation of bis-(4-chlorophenyl) sulfone |
| CN1623982A (zh) * | 2003-12-02 | 2005-06-08 | 马炳荣 | 4,4’-二氯二苯砜的制备方法 |
-
2011
- 2011-08-25 CN CN201110245933A patent/CN102304071A/zh active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0062736A1 (en) * | 1979-06-15 | 1982-10-20 | Amoco Corporation | Process for preparing 4-4'-dichlorodiphenyl sulphone |
| US4822916A (en) * | 1987-09-21 | 1989-04-18 | Akzo America Inc. | Preparation of diaryl sulfones |
| US4983773A (en) * | 1988-10-19 | 1991-01-08 | Basf Aktiengesellschaft | Preparation of bis-(4-chlorophenyl) sulfone |
| EP0381045A2 (de) * | 1989-02-01 | 1990-08-08 | BASF Aktiengesellschaft | Verfahren zur Herstellung von Bis-(4-chlorphenyl)-sulfon |
| CN1623982A (zh) * | 2003-12-02 | 2005-06-08 | 马炳荣 | 4,4’-二氯二苯砜的制备方法 |
Non-Patent Citations (4)
| Title |
|---|
| 《大连工学院学报》 19871231 李忠义,吴宝庆 4,4'-二氯二苯砜合成新工艺 第98页1对-氯苯磺酸的制备,24,4-二氯二苯砜的制备) 1 第26卷, * |
| 《辽宁化工》 19951231 高亚彪 4,4'-二氯二苯砜制备技术 第24页左栏1实验部分 1 , 第6期 * |
| 李忠义,吴宝庆: "4,4’-二氯二苯砜合成新工艺", 《大连工学院学报》 * |
| 高亚彪: "4,4’-二氯二苯砜制备技术", 《辽宁化工》 * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012143279A1 (en) * | 2011-04-18 | 2012-10-26 | Solvay Specialty Polymers Usa, Llc | Process for the manufacture of dihalodiphenylsulfones starting from organic acids |
| US9388128B2 (en) | 2011-04-18 | 2016-07-12 | Solvay Speciality Polymers Usa, Llc | Process for the manufacture of dihalodiphenylsulfones starting from organic acids |
| US9394248B2 (en) | 2011-04-18 | 2016-07-19 | Solvay Specialty Polymers Usa, Llc | Process for the manufacture of dihalodiphenylsulfones |
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Application publication date: 20120104 |