CN106008367A - Synthesis method of azoxystrobin - Google Patents

Synthesis method of azoxystrobin Download PDF

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Publication number
CN106008367A
CN106008367A CN201510803481.4A CN201510803481A CN106008367A CN 106008367 A CN106008367 A CN 106008367A CN 201510803481 A CN201510803481 A CN 201510803481A CN 106008367 A CN106008367 A CN 106008367A
Authority
CN
China
Prior art keywords
azoxystrobin
synthesis method
present
fluoxastrobin
synthetic method
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.)
Pending
Application number
CN201510803481.4A
Other languages
Chinese (zh)
Inventor
于国权
丁华平
吉志扬
王欣
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JIANGSU CHANGQING AGRICULTURAL CHEMISTRY CO Ltd
Original Assignee
JIANGSU CHANGQING AGRICULTURAL CHEMISTRY CO Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by JIANGSU CHANGQING AGRICULTURAL CHEMISTRY CO Ltd filed Critical JIANGSU CHANGQING AGRICULTURAL CHEMISTRY CO Ltd
Priority to CN201510803481.4A priority Critical patent/CN106008367A/en
Publication of CN106008367A publication Critical patent/CN106008367A/en
Pending legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms

Abstract

The invention relates to a synthesis method of azoxystrobin. Innovatively, the method provided by the invention uses clean dimethyl carbonate to replace the traditional high toxic dimethyl sulfate to serve as a methylation reagent, not only increases the single-step yield from 80% to 90%, but also realizes clean production.

Description

Fluoxastrobin synthetic method
Technical field
The present invention relates to a kind of Fluoxastrobin synthetic method, belong to technical field of pesticide.
Background technology
Fluoxastrobin is a kind of efficient, wide spectrum, new type bactericide; have Uptake and translocation, prevent, protect, the multiple action such as treatment; sprouting and the generation of almost all of mycota (Ascomycotina, Basidiomycotina, Mastigomycotina and Deuteromycotina) pathogenic bacteria spore can be suppressed, it is possible to control mycelial growth.And may also suppress Spores to invade; there is good protection activity; effectively control the various fungal diseases of the plants such as vegetable, fruit tree, flowers, such as powdery mildew, downy mildew, scab, anthrax, rust, epidemic disease, glume blight, net blotch, rice blast etc. comprehensively.Especially powdery mildew of strawberry, melon powdery mildew, powdery mildew of cucumber, pear scab there is specially good effect.
Therefore a kind of cleaning is provided to produce and improve the Fluoxastrobin synthetic method of yield and just seem highly desired.
Summary of the invention
The present invention is directed to drawbacks described above, it is therefore intended that provide one can improve yield, it is achieved the Fluoxastrobin synthetic method that cleaning produces.
For this technical solution used in the present invention it is:
The invention have the advantage that the present invention innovates uses cleaning dimethyl carbonate to replace traditional high poison dimethyl sulfate to make methylating reagent, not only improves single step yield and brings up to 90% from 80%, and achieves cleaning and produce.
Detailed description of the invention
The technical solution used in the present invention is:
It is an object of the invention to provide a kind of new synthetic route, content and correlated response condition (such as temperature, response time etc.) as component each in raw material all can be obtained by conventional means, it is not the innovative point of the present invention, is not described.
Through actually detected, generally can reach more than 92% according to the method fenoxanil condensation yield of synthetic route of the present invention, individual other can reach more than 95%, therefore the synthetic route of the present invention provides a kind of brand-new synthetic method, has great using value.

Claims (1)

1. Fluoxastrobin synthetic method, it is characterised in that follow the steps below:
CN201510803481.4A 2015-11-20 2015-11-20 Synthesis method of azoxystrobin Pending CN106008367A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510803481.4A CN106008367A (en) 2015-11-20 2015-11-20 Synthesis method of azoxystrobin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510803481.4A CN106008367A (en) 2015-11-20 2015-11-20 Synthesis method of azoxystrobin

Publications (1)

Publication Number Publication Date
CN106008367A true CN106008367A (en) 2016-10-12

Family

ID=57082380

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510803481.4A Pending CN106008367A (en) 2015-11-20 2015-11-20 Synthesis method of azoxystrobin

Country Status (1)

Country Link
CN (1) CN106008367A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1206401A (en) * 1996-02-17 1999-01-27 巴斯福股份公司 Process for preparing 2-(2-methylphenyl)-3-methoxyacrylic acid methylester
CN101157657A (en) * 2007-10-24 2008-04-09 北京颖新泰康科技有限公司 Method for preparing azoxystrobin and its analogue
CN103030598A (en) * 2012-12-17 2013-04-10 上海禾本药业有限公司 Method for preparing strobilurin fungicide
WO2014190997A1 (en) * 2013-05-28 2014-12-04 Cheminova A/S Process for preparing 4,6-bis(aryloxy)pyrimidine derivatives

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1206401A (en) * 1996-02-17 1999-01-27 巴斯福股份公司 Process for preparing 2-(2-methylphenyl)-3-methoxyacrylic acid methylester
CN101157657A (en) * 2007-10-24 2008-04-09 北京颖新泰康科技有限公司 Method for preparing azoxystrobin and its analogue
CN103030598A (en) * 2012-12-17 2013-04-10 上海禾本药业有限公司 Method for preparing strobilurin fungicide
WO2014190997A1 (en) * 2013-05-28 2014-12-04 Cheminova A/S Process for preparing 4,6-bis(aryloxy)pyrimidine derivatives

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
贾新明,等: "DMC在有机合成中的应用研究进展", 《广东化工》 *

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SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20161012

RJ01 Rejection of invention patent application after publication