ZA200607465B - Process for purifying mesotrione - Google Patents
Process for purifying mesotrione Download PDFInfo
- Publication number
- ZA200607465B ZA200607465B ZA200607465A ZA200607465A ZA200607465B ZA 200607465 B ZA200607465 B ZA 200607465B ZA 200607465 A ZA200607465 A ZA 200607465A ZA 200607465 A ZA200607465 A ZA 200607465A ZA 200607465 B ZA200607465 B ZA 200607465B
- Authority
- ZA
- South Africa
- Prior art keywords
- mesotrione
- sample
- aqueous solution
- cyanide
- distillation
- Prior art date
Links
- 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 claims description 37
- 239000005578 Mesotrione Substances 0.000 title claims description 36
- 238000000034 method Methods 0.000 title claims description 27
- 239000007864 aqueous solution Substances 0.000 claims description 17
- 238000004821 distillation Methods 0.000 claims description 16
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 14
- 238000002425 crystallisation Methods 0.000 claims description 12
- 239000003125 aqueous solvent Substances 0.000 claims description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 239000000243 solution Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 238000006462 rearrangement reaction Methods 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- SKDDBIWRHFHMKM-UHFFFAOYSA-N 4-methylsulfonyl-2-nitrobenzoyl chloride Chemical compound CS(=O)(=O)C1=CC=C(C(Cl)=O)C([N+]([O-])=O)=C1 SKDDBIWRHFHMKM-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000002825 nitriles Chemical group 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- 230000008707 rearrangement Effects 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- OXBDLEXAVKAJFD-UHFFFAOYSA-N 1-methyl-4-methylsulfonyl-2-nitrobenzene Chemical compound CC1=CC=C(S(C)(=O)=O)C=C1[N+]([O-])=O OXBDLEXAVKAJFD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- MWFMGBPGAXYFAR-UHFFFAOYSA-N 2-hydroxy-2-methylpropanenitrile Chemical compound CC(C)(O)C#N MWFMGBPGAXYFAR-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 235000005822 corn Nutrition 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
- -1 enol ester Chemical class 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/24—Sulfones; Sulfoxides having sulfone or sulfoxide groups and doubly-bound oxygen atoms bound to the same carbon skeleton
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/02—Sulfones; Sulfoxides having sulfone or sulfoxide groups bound to acyclic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0406894.6A GB0406894D0 (en) | 2004-03-26 | 2004-03-26 | Process |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200607465B true ZA200607465B (en) | 2008-05-28 |
Family
ID=32188804
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200607465A ZA200607465B (en) | 2004-03-26 | 2006-09-06 | Process for purifying mesotrione |
Country Status (29)
Country | Link |
---|---|
US (1) | US7863482B2 (pt) |
EP (1) | EP1740534B1 (pt) |
JP (1) | JP4690388B2 (pt) |
KR (1) | KR101147281B1 (pt) |
CN (1) | CN100475788C (pt) |
AR (1) | AR048040A1 (pt) |
AT (1) | ATE394369T1 (pt) |
AU (1) | AU2005225485B2 (pt) |
BR (1) | BRPI0509263B1 (pt) |
CA (1) | CA2558077C (pt) |
CY (1) | CY1108079T1 (pt) |
DE (1) | DE602005006550D1 (pt) |
DK (1) | DK1740534T3 (pt) |
ES (1) | ES2304003T3 (pt) |
GB (1) | GB0406894D0 (pt) |
GT (1) | GT200500066A (pt) |
HN (1) | HN2005000114A (pt) |
IL (1) | IL177723A (pt) |
MX (1) | MXPA06010765A (pt) |
MY (1) | MY146013A (pt) |
PL (1) | PL1740534T3 (pt) |
PT (1) | PT1740534E (pt) |
RU (1) | RU2373193C2 (pt) |
SI (1) | SI1740534T1 (pt) |
SV (1) | SV2006002057A (pt) |
TW (1) | TWI363750B (pt) |
UA (1) | UA83737C2 (pt) |
WO (1) | WO2005092846A1 (pt) |
ZA (1) | ZA200607465B (pt) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0419075D0 (en) | 2004-08-26 | 2004-09-29 | Syngenta Participations Ag | Process |
WO2007083242A1 (en) * | 2006-01-18 | 2007-07-26 | Syngenta Participations Ag | Process for the crystallisation of mesotrione |
JP4124793B2 (ja) * | 2006-06-09 | 2008-07-23 | 美津濃株式会社 | 手袋 |
CN102649774A (zh) * | 2012-02-02 | 2012-08-29 | 北京颖泰嘉和生物科技有限公司 | 一种降低磺草酮中氰化物的方法 |
CN103588685B (zh) * | 2013-10-18 | 2016-01-13 | 浙江省诸暨合力化学对外贸易有限公司 | 三酮类铵盐化合物及其制备方法及应用 |
CN104086438B (zh) * | 2014-06-30 | 2016-07-06 | 浙江中山化工集团股份有限公司 | 一种甲基磺草酮溶剂回收工艺 |
GB2530838B (en) | 2015-06-08 | 2020-01-22 | Rotam Agrochem Int Co Ltd | Process for purifying mesotrione |
CN110078647B (zh) * | 2019-05-15 | 2021-04-13 | 北京颖泰嘉和生物科技股份有限公司 | 一种硝磺草酮反应产物的后处理方法 |
CN111440099B (zh) * | 2020-04-09 | 2022-01-04 | 利民化学有限责任公司 | 一种环磺酮产品的纯化方法 |
CN112939826B (zh) * | 2021-02-05 | 2023-04-07 | 浙江工业大学 | 利用大孔吸附树脂从反应液中提取分离硝磺草酮的方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5085688A (en) * | 1982-03-25 | 1992-02-04 | Ici Americas Inc. | Certain 2-(2-chloro-3-alkoxy-4-substituted benzoyl)-5-methyl-5-1,3-cyclohexanediones as herbicides |
US4695673A (en) * | 1985-11-20 | 1987-09-22 | Stauffer Chemical Company | Process for the production of acylated 1,3-dicarbonyl compounds |
JPH0219355A (ja) * | 1988-07-07 | 1990-01-23 | Nippon Soda Co Ltd | 4,4,5−トリメチル−2−(2−ニトロ−4−メチルスルホニルベンゾイル)シクロヘキサン−1,3−ジオン、その製造方法及び除草剤 |
GB9725135D0 (en) * | 1997-11-27 | 1998-01-28 | Zeneca Ltd | Chemical process |
US7285678B2 (en) * | 2001-03-26 | 2007-10-23 | Syngenta Limited | Purification of 2-nitro-4-methylsulphonylbenzoic acid |
TWI348999B (en) * | 2003-10-02 | 2011-09-21 | Syngenta Participations Ag | Process |
-
2004
- 2004-03-26 GB GBGB0406894.6A patent/GB0406894D0/en not_active Ceased
-
2005
- 2005-03-03 DK DK05707695T patent/DK1740534T3/da active
- 2005-03-03 DE DE602005006550T patent/DE602005006550D1/de active Active
- 2005-03-03 US US10/598,993 patent/US7863482B2/en active Active
- 2005-03-03 AU AU2005225485A patent/AU2005225485B2/en active Active
- 2005-03-03 KR KR1020067019799A patent/KR101147281B1/ko active IP Right Grant
- 2005-03-03 JP JP2007504283A patent/JP4690388B2/ja active Active
- 2005-03-03 SI SI200530277T patent/SI1740534T1/sl unknown
- 2005-03-03 BR BRPI0509263-9A patent/BRPI0509263B1/pt active IP Right Grant
- 2005-03-03 UA UAA200611159A patent/UA83737C2/ru unknown
- 2005-03-03 CN CNB2005800098808A patent/CN100475788C/zh active Active
- 2005-03-03 ES ES05707695T patent/ES2304003T3/es active Active
- 2005-03-03 PT PT05707695T patent/PT1740534E/pt unknown
- 2005-03-03 AT AT05707695T patent/ATE394369T1/de active
- 2005-03-03 WO PCT/EP2005/002230 patent/WO2005092846A1/en active IP Right Grant
- 2005-03-03 EP EP05707695A patent/EP1740534B1/en active Active
- 2005-03-03 RU RU2006137659/04A patent/RU2373193C2/ru active
- 2005-03-03 MX MXPA06010765A patent/MXPA06010765A/es active IP Right Grant
- 2005-03-03 PL PL05707695T patent/PL1740534T3/pl unknown
- 2005-03-03 CA CA2558077A patent/CA2558077C/en active Active
- 2005-03-07 TW TW094106794A patent/TWI363750B/zh not_active IP Right Cessation
- 2005-03-15 AR ARP050101005A patent/AR048040A1/es active IP Right Grant
- 2005-03-18 SV SV2005002057A patent/SV2006002057A/es unknown
- 2005-03-18 HN HN2005000114A patent/HN2005000114A/es unknown
- 2005-03-22 GT GT200500066A patent/GT200500066A/es unknown
- 2005-03-24 MY MYPI20051287A patent/MY146013A/en unknown
-
2006
- 2006-08-28 IL IL177723A patent/IL177723A/en active IP Right Grant
- 2006-09-06 ZA ZA200607465A patent/ZA200607465B/en unknown
-
2008
- 2008-05-20 CY CY20081100522T patent/CY1108079T1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ZA200607465B (en) | Process for purifying mesotrione | |
ZA200601864B (en) | Process for purifying mesotrione | |
CA2296996C (en) | Purification of lipstatin | |
ATE263145T1 (de) | Verfahren zur herstellung von n-carbamat- geschütztem beta-aminoepoxid und beta- aminoalkohol | |
DK1682497T3 (en) | PROCEDURE FOR PURIFYING MESOTRION | |
Brimble et al. | Synthesis and ene reactions of di-(−)-menthyl diazenedicarboxylate | |
CA2624934C (en) | Preparing method for amorphous lercanidipine | |
JP2020502068A (ja) | メタクリル酸メチルの調製のために洗浄沈降機内でn−オキシル重合阻害剤を使用する方法 | |
CN111269195A (zh) | 一种制备糖精的合成方法 | |
EP4013747B1 (en) | Reduction of the odor of monothiocarbonate compounds by addition of oxidants | |
CN113727976B (zh) | 一种缬沙坦化合物的精制方法 | |
JP2003160580A (ja) | エチレンサルファイト及びその製造方法 |