CN100369883C - 邻氯苯甲酸和对氯苯甲酸混合物的分离方法 - Google Patents
邻氯苯甲酸和对氯苯甲酸混合物的分离方法 Download PDFInfo
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- CN100369883C CN100369883C CNB2006100856489A CN200610085648A CN100369883C CN 100369883 C CN100369883 C CN 100369883C CN B2006100856489 A CNB2006100856489 A CN B2006100856489A CN 200610085648 A CN200610085648 A CN 200610085648A CN 100369883 C CN100369883 C CN 100369883C
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- CN
- China
- Prior art keywords
- acid
- chloro
- chlorodracylic
- benzoic acid
- mixture
- 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.)
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- XRHGYUZYPHTUJZ-UHFFFAOYSA-N 4-chlorobenzoic acid Chemical compound OC(=O)C1=CC=C(Cl)C=C1 XRHGYUZYPHTUJZ-UHFFFAOYSA-N 0.000 title claims abstract description 95
- 239000000203 mixture Substances 0.000 title claims abstract description 58
- 238000000926 separation method Methods 0.000 title abstract description 9
- IKCLCGXPQILATA-UHFFFAOYSA-N 2-chlorobenzoic acid Chemical compound OC(=O)C1=CC=CC=C1Cl IKCLCGXPQILATA-UHFFFAOYSA-N 0.000 title abstract description 6
- 239000000706 filtrate Substances 0.000 claims abstract description 38
- 239000012065 filter cake Substances 0.000 claims abstract description 31
- 230000002378 acidificating effect Effects 0.000 claims abstract description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 25
- 238000001914 filtration Methods 0.000 claims abstract description 23
- 238000006243 chemical reaction Methods 0.000 claims abstract description 17
- 238000013019 agitation Methods 0.000 claims abstract description 7
- 238000001035 drying Methods 0.000 claims abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 21
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 20
- 238000001291 vacuum drying Methods 0.000 claims description 19
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Substances [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 10
- 239000002994 raw material Substances 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 9
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 8
- 239000000243 solution Substances 0.000 claims description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 6
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 235000021463 dry cake Nutrition 0.000 claims description 4
- 235000019253 formic acid Nutrition 0.000 claims description 4
- 229910017604 nitric acid Inorganic materials 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
- 239000011707 mineral Substances 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims 2
- 239000003513 alkali Substances 0.000 claims 1
- 230000035484 reaction time Effects 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 13
- 238000005265 energy consumption Methods 0.000 abstract description 5
- 230000000694 effects Effects 0.000 abstract 1
- 238000003756 stirring Methods 0.000 description 25
- 238000004587 chromatography analysis Methods 0.000 description 16
- 239000007791 liquid phase Substances 0.000 description 16
- NPDACUSDTOMAMK-UHFFFAOYSA-N 4-Chlorotoluene Chemical compound CC1=CC=C(Cl)C=C1 NPDACUSDTOMAMK-UHFFFAOYSA-N 0.000 description 14
- 239000013078 crystal Substances 0.000 description 12
- 239000012467 final product Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- GHMWZRWCBLXYBX-UHFFFAOYSA-M sodium;4-chlorobenzoate Chemical compound [Na+].[O-]C(=O)C1=CC=C(Cl)C=C1 GHMWZRWCBLXYBX-UHFFFAOYSA-M 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 230000003165 hydrotropic effect Effects 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 3
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- -1 ester sodium salt Chemical class 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 229960003439 mebendazole Drugs 0.000 description 2
- BAXLBXFAUKGCDY-UHFFFAOYSA-N mebendazole Chemical compound [CH]1C2=NC(NC(=O)OC)=NC2=CC=C1C(=O)C1=CC=CC=C1 BAXLBXFAUKGCDY-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- MQSMIOKTOYAPHO-WEVVVXLNSA-N [(e)-5-hydroperoxypent-1-enyl]benzene Chemical compound OOCCC\C=C\C1=CC=CC=C1 MQSMIOKTOYAPHO-WEVVVXLNSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 238000001838 alkalimetric titration Methods 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- ZPEIMTDSQAKGNT-UHFFFAOYSA-N chlorpromazine Chemical compound C1=C(Cl)C=C2N(CCCN(C)C)C3=CC=CC=C3SC2=C1 ZPEIMTDSQAKGNT-UHFFFAOYSA-N 0.000 description 1
- 229960001076 chlorpromazine Drugs 0.000 description 1
- VNFPBHJOKIVQEB-UHFFFAOYSA-N clotrimazole Chemical compound ClC1=CC=CC=C1C(N1C=NC=C1)(C=1C=CC=CC=1)C1=CC=CC=C1 VNFPBHJOKIVQEB-UHFFFAOYSA-N 0.000 description 1
- 229960004022 clotrimazole Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- DCOPUUMXTXDBNB-UHFFFAOYSA-N diclofenac Chemical compound OC(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl DCOPUUMXTXDBNB-UHFFFAOYSA-N 0.000 description 1
- 229960001259 diclofenac Drugs 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 229960004500 flubendazole Drugs 0.000 description 1
- CPEUVMUXAHMANV-UHFFFAOYSA-N flubendazole Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1C(=O)C1=CC=C(F)C=C1 CPEUVMUXAHMANV-UHFFFAOYSA-N 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 description 1
- 238000009775 high-speed stirring Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 230000003637 steroidlike Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (9)
Priority Applications (1)
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CNB2006100856489A CN100369883C (zh) | 2006-06-28 | 2006-06-28 | 邻氯苯甲酸和对氯苯甲酸混合物的分离方法 |
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CNB2006100856489A CN100369883C (zh) | 2006-06-28 | 2006-06-28 | 邻氯苯甲酸和对氯苯甲酸混合物的分离方法 |
Publications (2)
Publication Number | Publication Date |
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CN1868995A CN1868995A (zh) | 2006-11-29 |
CN100369883C true CN100369883C (zh) | 2008-02-20 |
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CNB2006100856489A Expired - Fee Related CN100369883C (zh) | 2006-06-28 | 2006-06-28 | 邻氯苯甲酸和对氯苯甲酸混合物的分离方法 |
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Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102276449A (zh) * | 2010-06-11 | 2011-12-14 | 南通派斯第农药化工有限公司 | 4,4-二甲基-1-(4-氯苯基)-1-戊烯-3-酮合成废液处理工艺 |
CN107285993A (zh) * | 2017-06-22 | 2017-10-24 | 河南大学 | 一种酮苷固体废弃物资源化处理方法 |
CN114478234B (zh) * | 2022-02-09 | 2023-03-31 | 河北海力恒远新材料股份有限公司 | 一种4-氯代邻苯二甲酸单钠盐粗品的精制方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2546545A (en) * | 1950-12-22 | 1951-03-27 | Tennessee Products & Chemical | Process for the separation of isomeric chlorobenzoic acids |
CN1376140A (zh) * | 2000-07-27 | 2002-10-23 | 科技部 | 分离邻-和对-取代苯化合物的方法 |
-
2006
- 2006-06-28 CN CNB2006100856489A patent/CN100369883C/zh not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2546545A (en) * | 1950-12-22 | 1951-03-27 | Tennessee Products & Chemical | Process for the separation of isomeric chlorobenzoic acids |
CN1376140A (zh) * | 2000-07-27 | 2002-10-23 | 科技部 | 分离邻-和对-取代苯化合物的方法 |
Non-Patent Citations (3)
Title |
---|
Modelowanie procesu rozdzielania kwasow2-chlorobenzoesowego i 4-chlorobenzoesowego. STRYJEK R, ET AL.PRZEMYSL CHEMICZNY,Vol.69 No.9. 1990 * |
Separation of chlorobenzoic acids by dissociation extractivecrystallization. Asghar Lashanizadegan, et al.Chemical engineering science,Vol.56 . 2001 * |
Separation of close boiling organic acids and bases bydissociation extraction: chlorophenols, N-alkyl anilines andchlorobenzoic acids. Satish S. Laddha, et al.J. appl. chem. biotechnol.,Vol.28 . 1978 * |
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CN1868995A (zh) | 2006-11-29 |
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Owner name: NANJING TUOPU CHEMICAL CO., LTD Free format text: FORMER OWNER: QIAO XU Effective date: 20100919 |
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Free format text: CORRECT: ADDRESS; FROM: 210009 NO.82, XINSHENGYUAN, GULOU DISTRICT, NANJING CITY, JIANGSU PROVINCE TO: 210047 NO.179, WEST ZONE OF CHEMICAL INDUSTRIAL PARK, LIUHE DISTRICT, NANJING CITY, JIANGSU PROVINCE |
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Effective date of registration: 20100919 Address after: 210047 Nanjing Chemical Industrial Park, Liuhe District, Jiangsu, No. 179 Patentee after: NANJING TOP CHEMICAL Co.,Ltd. Address before: 210009 No. 82, Gulou District, Jiangsu, Nanjing Patentee before: Qiao Xu |
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Address after: 210047 Nanjing Chemical Industrial Park West Road, Jiangsu, No. 179 Patentee after: NANJING TOP CHEMICAL TECHNOLOGY Co.,Ltd. Address before: 210047 Nanjing Chemical Industrial Park, Liuhe District, Jiangsu, No. 179 Patentee before: NANJING TOP CHEMICAL Co.,Ltd. |
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Effective date of registration: 20220216 Address after: 211599 13 / F, main building, science and innovation center, 59 Wangqiao Road, Xiongzhou street, Liuhe District, Nanjing City, Jiangsu Province Patentee after: Nanjing Zihuan Engineering Technology Research Institute Co.,Ltd. Address before: 210047 No. 179 West Road, Nanjing Chemical Industrial Park, Jiangsu Patentee before: NANJING TOP CHEMICAL TECHNOLOGY Co.,Ltd. |
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CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20080220 |