UA79741C2 - Method for removing impurities from 2-nitro-4-methylsulfonylbenzoic acid, purified 2-nitro-4-methylsulphonylbenzoic acid and process for preparation of mesotrione - Google Patents
Method for removing impurities from 2-nitro-4-methylsulfonylbenzoic acid, purified 2-nitro-4-methylsulphonylbenzoic acid and process for preparation of mesotrione Download PDFInfo
- Publication number
- UA79741C2 UA79741C2 UA2003109605A UA2003109605A UA79741C2 UA 79741 C2 UA79741 C2 UA 79741C2 UA 2003109605 A UA2003109605 A UA 2003109605A UA 2003109605 A UA2003109605 A UA 2003109605A UA 79741 C2 UA79741 C2 UA 79741C2
- Authority
- UA
- Ukraine
- Prior art keywords
- nitro
- acid
- mesotrione
- methylsulfonylbenzoic acid
- methylsulfonylbenzoic
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract description 22
- 239000012535 impurity Substances 0.000 title abstract description 14
- QNOUABMNRMROSL-UHFFFAOYSA-N 110964-79-9 Chemical compound CS(=O)(=O)C1=CC=C(C(O)=O)C([N+]([O-])=O)=C1 QNOUABMNRMROSL-UHFFFAOYSA-N 0.000 title abstract description 13
- 239000005578 Mesotrione Substances 0.000 title description 18
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 title description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 9
- 238000001914 filtration Methods 0.000 abstract description 8
- 239000007864 aqueous solution Substances 0.000 abstract description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract description 2
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical group CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 20
- 239000000243 solution Substances 0.000 description 20
- 239000003245 coal Substances 0.000 description 14
- 239000007787 solid Substances 0.000 description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000000725 suspension Substances 0.000 description 10
- 238000011068 loading method Methods 0.000 description 8
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical class CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 7
- 238000010953 Ames test Methods 0.000 description 7
- 231100000039 Ames test Toxicity 0.000 description 7
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000008399 tap water Substances 0.000 description 6
- 235000020679 tap water Nutrition 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 239000012452 mother liquor Substances 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 3
- -1 2-nitro-4-nitrobenzoyl Chemical group 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- HJSLFCCWAKVHIW-UHFFFAOYSA-N cyclohexane-1,3-dione Chemical compound O=C1CCCC(=O)C1 HJSLFCCWAKVHIW-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000010413 mother solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- OILAIQUEIWYQPH-UHFFFAOYSA-N cyclohexane-1,2-dione Chemical compound O=C1CCCCC1=O OILAIQUEIWYQPH-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- SETMGIIITGNLAS-UHFFFAOYSA-N spizofurone Chemical compound O=C1C2=CC(C(=O)C)=CC=C2OC21CC2 SETMGIIITGNLAS-UHFFFAOYSA-N 0.000 description 1
- 229950001870 spizofurone Drugs 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- CZPRKINNVBONSF-UHFFFAOYSA-M zinc;dioxido(oxo)phosphanium Chemical compound [Zn+2].[O-][P+]([O-])=O CZPRKINNVBONSF-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C315/00—Preparation of sulfones; Preparation of sulfoxides
- C07C315/06—Separation; Purification; Stabilisation; Use of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US27506101P | 2001-03-26 | 2001-03-26 | |
| PCT/GB2002/001433 WO2002076934A2 (en) | 2001-03-26 | 2002-03-25 | Purification of 2-nitro-4-methylsulphonylbenzoic acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA79741C2 true UA79741C2 (en) | 2007-07-25 |
Family
ID=23050721
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2003109605A UA79741C2 (en) | 2001-03-26 | 2002-03-25 | Method for removing impurities from 2-nitro-4-methylsulfonylbenzoic acid, purified 2-nitro-4-methylsulphonylbenzoic acid and process for preparation of mesotrione |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US7285678B2 (ru) |
| EP (1) | EP1377544B2 (ru) |
| JP (1) | JP3911237B2 (ru) |
| KR (1) | KR100858546B1 (ru) |
| CN (1) | CN1250525C (ru) |
| AR (1) | AR033205A1 (ru) |
| AU (1) | AU2002249384B2 (ru) |
| BR (1) | BR0207414A (ru) |
| CA (1) | CA2434980C (ru) |
| CZ (1) | CZ303984B6 (ru) |
| DK (1) | DK1377544T4 (ru) |
| ES (1) | ES2488840T5 (ru) |
| GT (1) | GT200200060A (ru) |
| HU (1) | HU230861B1 (ru) |
| IL (2) | IL157176A0 (ru) |
| MX (1) | MXPA03008279A (ru) |
| PL (1) | PL363837A1 (ru) |
| PT (1) | PT1377544E (ru) |
| RU (1) | RU2287521C2 (ru) |
| SK (1) | SK11812003A3 (ru) |
| TW (1) | TWI224091B (ru) |
| UA (1) | UA79741C2 (ru) |
| WO (1) | WO2002076934A2 (ru) |
| ZA (1) | ZA200306327B (ru) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0323090D0 (en) * | 2003-10-02 | 2003-11-05 | Syngenta Participations Ag | Novel process |
| TWI348999B (en) * | 2003-10-02 | 2011-09-21 | Syngenta Participations Ag | Process |
| GB0406894D0 (en) * | 2004-03-26 | 2004-04-28 | Syngenta Participations Ag | Process |
| GB0419075D0 (en) * | 2004-08-26 | 2004-09-29 | Syngenta Participations Ag | Process |
| JP5149199B2 (ja) * | 2006-01-18 | 2013-02-20 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | メソトリオンの結晶化方法 |
| CN104059001B (zh) * | 2013-03-18 | 2016-06-08 | 华中师范大学 | 一种邻硝基砜基苯甲酸的制备方法 |
| CN103910659B (zh) * | 2013-11-04 | 2016-05-11 | 迈克斯(如东)化工有限公司 | 2-硝基-4-甲磺酰基苯甲酸的精制方法及其中间体 |
| US20160280641A1 (en) * | 2013-11-04 | 2016-09-29 | Yutian Shao | Method for refining 2-nito-4-methylsulfonyl benzoic acid and intermediate thereof |
| CN104829506B (zh) * | 2015-04-09 | 2016-08-17 | 浙江嘉化能源化工股份有限公司 | 高纯2-硝基-4-甲砜基苯甲酸的工业化生产方法 |
| GB2530838B (en) | 2015-06-08 | 2020-01-22 | Rotam Agrochem Int Co Ltd | Process for purifying mesotrione |
| JP2017137243A (ja) * | 2016-02-01 | 2017-08-10 | エア・ウォーター株式会社 | ２−ニトロ−４−メチルスルホニル安息香酸の製造方法 |
| CN105669504A (zh) * | 2016-03-07 | 2016-06-15 | 山东润博生物科技有限公司 | 一种2-硝基-4-甲砜基苯甲酸的制备方法 |
| CN106699616A (zh) * | 2016-11-17 | 2017-05-24 | 北京颖泰嘉和生物科技股份有限公司 | 一种新的2‑硝基‑4‑甲磺酰基苯甲酸的纯化方法 |
| CN111302987A (zh) * | 2018-12-12 | 2020-06-19 | 北京颖泰嘉和生物科技股份有限公司 | 2-硝基-4-甲磺酰基苯甲酸的精制方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5006158A (en) | 1984-12-20 | 1991-04-09 | Ici Americas Inc. | Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones |
| JP2849470B2 (ja) * | 1988-12-07 | 1999-01-20 | アイシーアイ アメリカズ インコーポレイテッド | ２―（クロロ，ブロモ，またはニトロ）―４―（アルキルスルフォニル）安息香酸の調製および中間体 |
| US5079381A (en) † | 1990-09-28 | 1992-01-07 | Imperial Chemical Industries Plc | Method for the preparation of 4-methylsulfonyl benzoic acid derivatives and intermediates |
| US5055605A (en) | 1990-10-15 | 1991-10-08 | Imperial Chemical Industries Plc | Preparation of trisubstituted benzoic acid precursors |
| DE4235155A1 (de) * | 1992-10-19 | 1994-04-21 | Basf Ag | Verfahren zur Herstellung von Methylsulfonylbenzoesäuren |
| US5591890A (en) † | 1995-11-03 | 1997-01-07 | E. I. Du Pont De Nemours And Company | Process for producing ortho-nitro aromatic acids by oxidation of ortho-nitroalkylaromatic compounds |
| GB9725135D0 (en) | 1997-11-27 | 1998-01-28 | Zeneca Ltd | Chemical process |
-
2002
- 2002-03-25 AR ARP020101080A patent/AR033205A1/es active IP Right Grant
- 2002-03-25 JP JP2002576196A patent/JP3911237B2/ja not_active Expired - Lifetime
- 2002-03-25 KR KR1020037011328A patent/KR100858546B1/ko not_active IP Right Cessation
- 2002-03-25 PT PT2718314T patent/PT1377544E/pt unknown
- 2002-03-25 MX MXPA03008279A patent/MXPA03008279A/es active IP Right Grant
- 2002-03-25 GT GT200200060A patent/GT200200060A/es unknown
- 2002-03-25 US US10/472,962 patent/US7285678B2/en not_active Expired - Lifetime
- 2002-03-25 RU RU2003131328/04A patent/RU2287521C2/ru active
- 2002-03-25 IL IL15717602A patent/IL157176A0/xx unknown
- 2002-03-25 ES ES02718314.4T patent/ES2488840T5/es not_active Expired - Lifetime
- 2002-03-25 DK DK02718314.4T patent/DK1377544T4/en active
- 2002-03-25 BR BR0207414-1A patent/BR0207414A/pt not_active Application Discontinuation
- 2002-03-25 SK SK1181-2003A patent/SK11812003A3/sk not_active Application Discontinuation
- 2002-03-25 HU HU0302530A patent/HU230861B1/hu unknown
- 2002-03-25 AU AU2002249384A patent/AU2002249384B2/en not_active Expired
- 2002-03-25 EP EP02718314.4A patent/EP1377544B2/en not_active Expired - Lifetime
- 2002-03-25 CA CA2434980A patent/CA2434980C/en not_active Expired - Lifetime
- 2002-03-25 WO PCT/GB2002/001433 patent/WO2002076934A2/en active IP Right Grant
- 2002-03-25 UA UA2003109605A patent/UA79741C2/uk unknown
- 2002-03-25 CZ CZ20032548A patent/CZ303984B6/cs not_active IP Right Cessation
- 2002-03-25 CN CNB028072030A patent/CN1250525C/zh not_active Expired - Lifetime
- 2002-03-25 PL PL02363837A patent/PL363837A1/xx not_active Application Discontinuation
- 2002-07-02 TW TW091114621A patent/TWI224091B/zh not_active IP Right Cessation
-
2003
- 2003-07-30 IL IL157176A patent/IL157176A/en active IP Right Grant
- 2003-08-14 ZA ZA200306327A patent/ZA200306327B/xx unknown
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