EA201892211A3 - Способ получения азоксистробина - Google Patents
Способ получения азоксистробинаInfo
- Publication number
- EA201892211A3 EA201892211A3 EA201892211A EA201892211A EA201892211A3 EA 201892211 A3 EA201892211 A3 EA 201892211A3 EA 201892211 A EA201892211 A EA 201892211A EA 201892211 A EA201892211 A EA 201892211A EA 201892211 A3 EA201892211 A3 EA 201892211A3
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- azoxystrobin
- producing
- yield
- reduces
- formula
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
- B01J31/0235—Nitrogen containing compounds
- B01J31/0237—Amines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/31—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of functional groups containing oxygen only in singly bound form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/317—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
В настоящем изобретении предусмотрен способ получения азоксистробина, который осуществляют путем проведения реакции между 2-цианофенолом или его солью и соединением, представленным формулой I, при катализе с помощью триметиламинового катализатора с получением азоксистробина, представленного формулой II, который обеспечивает выход продукта, представляющего собой азоксистробин, составляющий 98% или больше, выход отделенного продукта, составляющий 95% или больше, и упрощение последующей обработки. Триметиламиновый катализатор можно регенерировать и повторно использовать в осуществлении синтеза целевого продукта, представляющего собой азоксистробин, что не только снижает стоимость, но также снижает содержание общего азота и COD в отработанной воде. Преимущества способа согласно настоящему изобретению в отношении стоимости и защиты окружающей среды являются значительными и, таким образом, данный способ является пригодным для промышленного производства.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201711049391.6A CN109721548B (zh) | 2017-10-31 | 2017-10-31 | 一种嘧菌酯的制备方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EA201892211A2 EA201892211A2 (ru) | 2019-06-28 |
| EA201892211A3 true EA201892211A3 (ru) | 2019-10-31 |
| EA036663B1 EA036663B1 (ru) | 2020-12-04 |
Family
ID=61167935
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201892211A EA036663B1 (ru) | 2017-10-31 | 2018-10-30 | Способ получения азоксистробина |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US10189793B1 (ru) |
| EP (1) | EP3476838B1 (ru) |
| JP (1) | JP6714062B2 (ru) |
| KR (1) | KR102132087B1 (ru) |
| CN (1) | CN109721548B (ru) |
| AR (1) | AR113809A1 (ru) |
| AU (1) | AU2018250429B9 (ru) |
| BR (1) | BR102018002942B1 (ru) |
| CA (1) | CA3022444C (ru) |
| DK (1) | DK3476838T3 (ru) |
| EA (1) | EA036663B1 (ru) |
| ES (1) | ES2767961T3 (ru) |
| IL (1) | IL262340B (ru) |
| LT (1) | LT3476838T (ru) |
| NZ (1) | NZ747412A (ru) |
| PL (1) | PL3476838T3 (ru) |
| PT (1) | PT3476838T (ru) |
| SI (1) | SI3476838T1 (ru) |
| TW (1) | TWI688558B (ru) |
| UA (1) | UA120414C2 (ru) |
| ZA (1) | ZA201807239B (ru) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102786122B1 (ko) * | 2019-09-23 | 2025-03-24 | 주식회사 엘지화학 | 화합물의 제조방법 |
| KR102884226B1 (ko) * | 2020-09-10 | 2025-11-10 | 주식회사 엘지화학 | 아족시스트로빈의 정제방법 |
| CN114685376B (zh) * | 2020-12-28 | 2024-06-07 | 北京颖泰嘉和生物科技股份有限公司 | 嘧菌酯中间体的制备方法 |
| CN114685377B (zh) * | 2020-12-31 | 2024-05-31 | 北京颖泰嘉和生物科技股份有限公司 | 嘧菌酯类化合物的制备方法 |
| CN114195723A (zh) * | 2021-11-30 | 2022-03-18 | 江苏七洲绿色科技研究院有限公司 | 一种嘧菌酯的制备方法 |
| CN117548142A (zh) * | 2022-08-04 | 2024-02-13 | 北京颖泰嘉和生物科技股份有限公司 | 一种组合物及其应用 |
| CN120383567A (zh) * | 2024-12-31 | 2025-07-29 | 内蒙古灵圣作物科技有限公司 | 一种嘧菌酯的合成方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL106324A (en) * | 1992-07-17 | 1998-09-24 | Shell Int Research | Transformed pyrimidine compounds, their preparation and use as pesticides |
| UA53611C2 (ru) | 1996-03-07 | 2003-02-17 | Амерікан Ціанамід Компані | Способ получения несиметричных 4,6-бис(арилокси)пиримидиновых соединений |
| US5849910A (en) * | 1997-09-05 | 1998-12-15 | American Cyanamid Company | Process for the preparation of unsymmetrical 4,6-bis aryloxy-pyrimidine compounds |
| GB0508422D0 (en) | 2005-04-26 | 2005-06-01 | Syngenta Ltd | Chemical process |
| GB0619941D0 (en) * | 2006-10-09 | 2006-11-15 | Syngenta Ltd | Chemical process |
| GB0619942D0 (en) | 2006-10-09 | 2006-11-15 | Syngenta Ltd | Chemical process |
| CN102516122B (zh) * | 2011-11-08 | 2014-11-05 | 上海禾本药业有限公司 | 制备邻羟基苯甲腈的dmf溶液的方法 |
| KR101469879B1 (ko) * | 2012-12-27 | 2014-12-05 | 동부팜한농 주식회사 | 메틸 (e)-2-[2-[6-(2-시아노페녹시)피리미딘-4-일옥시]페닐]-3-메톡시아크릴레이트를 제조하는 방법 |
| CN103145627B (zh) | 2013-02-28 | 2015-10-07 | 河北威远生化农药有限公司 | 一种嘧菌酯的合成方法 |
| CN103265496B (zh) * | 2013-05-16 | 2015-02-25 | 北京颖泰嘉和生物科技有限公司 | 一种嘧菌酯的制备方法 |
| TWI621614B (zh) * | 2013-05-28 | 2018-04-21 | 科麥農股份有限公司 | 4,6-雙(芳氧基)嘧啶衍生物的製備方法 |
| CN104230820B (zh) | 2014-09-16 | 2016-09-28 | 重庆紫光国际化工有限责任公司 | 嘧菌酯的合成方法 |
-
2017
- 2017-10-31 CN CN201711049391.6A patent/CN109721548B/zh active Active
-
2018
- 2018-01-12 US US15/869,205 patent/US10189793B1/en active Active
- 2018-02-06 PL PL18155233T patent/PL3476838T3/pl unknown
- 2018-02-06 EP EP18155233.2A patent/EP3476838B1/en active Active
- 2018-02-06 SI SI201830025T patent/SI3476838T1/sl unknown
- 2018-02-06 LT LTEP18155233.2T patent/LT3476838T/lt unknown
- 2018-02-06 PT PT181552332T patent/PT3476838T/pt unknown
- 2018-02-06 DK DK18155233.2T patent/DK3476838T3/da active
- 2018-02-06 ES ES18155233T patent/ES2767961T3/es active Active
- 2018-02-15 BR BR102018002942-8A patent/BR102018002942B1/pt active IP Right Grant
- 2018-10-14 IL IL262340A patent/IL262340B/en active IP Right Grant
- 2018-10-18 AU AU2018250429A patent/AU2018250429B9/en active Active
- 2018-10-18 NZ NZ74741218A patent/NZ747412A/en unknown
- 2018-10-26 TW TW107137989A patent/TWI688558B/zh active
- 2018-10-29 CA CA3022444A patent/CA3022444C/en active Active
- 2018-10-30 AR ARP180103152A patent/AR113809A1/es active IP Right Grant
- 2018-10-30 KR KR1020180131012A patent/KR102132087B1/ko active Active
- 2018-10-30 EA EA201892211A patent/EA036663B1/ru unknown
- 2018-10-30 UA UAA201810721A patent/UA120414C2/uk unknown
- 2018-10-30 ZA ZA2018/07239A patent/ZA201807239B/en unknown
- 2018-10-31 JP JP2018205286A patent/JP6714062B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| PT3476838T (pt) | 2020-02-19 |
| CN109721548B (zh) | 2020-11-13 |
| US10189793B1 (en) | 2019-01-29 |
| KR20190049568A (ko) | 2019-05-09 |
| TW201918475A (zh) | 2019-05-16 |
| LT3476838T (lt) | 2020-01-27 |
| EP3476838A1 (en) | 2019-05-01 |
| EA201892211A2 (ru) | 2019-06-28 |
| SI3476838T1 (sl) | 2020-02-28 |
| KR102132087B1 (ko) | 2020-07-09 |
| EP3476838B1 (en) | 2019-11-13 |
| JP2019081758A (ja) | 2019-05-30 |
| AR113809A1 (es) | 2020-06-10 |
| UA120414C2 (uk) | 2019-11-25 |
| CN109721548A (zh) | 2019-05-07 |
| CA3022444C (en) | 2020-09-22 |
| EA036663B1 (ru) | 2020-12-04 |
| IL262340B (en) | 2021-01-31 |
| AU2018250429A1 (en) | 2019-05-16 |
| IL262340A (en) | 2019-02-28 |
| BR102018002942A2 (pt) | 2019-06-04 |
| AU2018250429B2 (en) | 2019-08-15 |
| BR102018002942B1 (pt) | 2020-11-10 |
| DK3476838T3 (da) | 2020-02-10 |
| ES2767961T3 (es) | 2020-06-19 |
| ZA201807239B (en) | 2019-07-31 |
| JP6714062B2 (ja) | 2020-06-24 |
| AU2018250429B9 (en) | 2019-10-31 |
| CA3022444A1 (en) | 2019-04-30 |
| TWI688558B (zh) | 2020-03-21 |
| PL3476838T3 (pl) | 2020-05-18 |
| NZ747412A (en) | 2019-11-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EA201892211A3 (ru) | Способ получения азоксистробина | |
| NZ747549A (en) | Method for preparing azoxystrobin intermediates | |
| EA201891657A1 (ru) | Интегрированный процесс ферментации и электролиза | |
| MY165219A (en) | Process for production of hexamethylenediamine from 5 - hydroxymethylfurfural | |
| MX2017007339A (es) | Proceso para la producción de 2,5-bis-hidroximetilfurano, 2,5-bis-hidroximetiltetrahidrofurano, 1,6-hexanodiol y 1,2,6-hexanotriol a partir de 5-hidroximetilfurfural. | |
| MX2020006306A (es) | Método novedoso para producir 4,5-dihidroisoxazol 5,5-disustituido. | |
| CY1120380T1 (el) | Διαδικασια για την παρασκευη παραγωγων 4,6-δις(αρυλοξυ)πυριμιδινης | |
| CA2864676C (en) | Methods and kits for reducing non-specific nucleic acid amplification | |
| EA201992709A1 (ru) | Способ получения оптически активного соединения | |
| EA202091466A1 (ru) | Синтез сокристалла 1:1:1 1-циано-2-(4-циклопропилбензил)-4-(-d-глюкопираноз-1-ил)бензола, l-пролина и воды | |
| EA201990731A1 (ru) | Способ получения гликолевой кислоты | |
| AU2012329618A8 (en) | Process for the conversion of lignocellulose material into an organic acid | |
| UA120052C2 (uk) | Спосіб і установка для синтезу сечовини і меламіну | |
| EP4410773A3 (en) | Process for the synthesis of (s) 3-amino-4-(difluoromethylenyl)cyclopent-1-ene-1-carboxylic acid | |
| MY185374A (en) | Preparation method for aryl substituted p-phenylenediamine substance | |
| ZA202102282B (en) | Method to modify the surface of a molecular sieve with an aminosilane | |
| EA201000129A1 (ru) | Способ диафрагмализа и применение полученных этим способом продуктов | |
| BR112023000029A2 (pt) | Método de preparação do composto de fenilisoxazolina | |
| EA201890795A1 (ru) | Способ прямого получения диметилового эфира гликоля и совместного получения этиленгликоля из монометилового эфира этиленгликоля | |
| EA201791374A1 (ru) | Способ производства карбамида | |
| EA200700125A1 (ru) | Способ промышленного получения ароматического карбоната | |
| MY182164A (en) | Process for producing acetic acid by introducing a lithium compound | |
| EA202092880A1 (ru) | Получение hmf, катализируемое фракцией анолита | |
| FR2973377B1 (fr) | Derives de la 2,9-dipyridyl-1,10-phenanthroline utiles comme ligands des actinides, leur procede de synthese et leurs utilisations | |
| MX2018007379A (es) | Proceso para la purificacion de metacrilato de metilo. |