CN108059606A - 一种利用尿素制备氰氟虫腙中间体的方法 - Google Patents
一种利用尿素制备氰氟虫腙中间体的方法 Download PDFInfo
- Publication number
- CN108059606A CN108059606A CN201810114496.3A CN201810114496A CN108059606A CN 108059606 A CN108059606 A CN 108059606A CN 201810114496 A CN201810114496 A CN 201810114496A CN 108059606 A CN108059606 A CN 108059606A
- Authority
- CN
- China
- Prior art keywords
- benzene
- trifluoromethoxy
- urea
- trifluoromethoxyphen
- halogenated
- 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.)
- Granted
Links
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 title claims abstract description 16
- 239000004202 carbamide Substances 0.000 title claims abstract description 16
- 238000000034 method Methods 0.000 title claims abstract description 13
- MIFOMMKAVSCNKQ-HWIUFGAZSA-N Metaflumizone Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)N\N=C(C=1C=C(C=CC=1)C(F)(F)F)\CC1=CC=C(C#N)C=C1 MIFOMMKAVSCNKQ-HWIUFGAZSA-N 0.000 title claims abstract description 10
- 239000005914 Metaflumizone Substances 0.000 title claims abstract description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 33
- DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 claims abstract description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 238000006243 chemical reaction Methods 0.000 claims abstract description 11
- 239000007787 solid Substances 0.000 claims abstract description 7
- 239000005457 ice water Substances 0.000 claims abstract description 5
- 238000010992 reflux Methods 0.000 claims abstract description 5
- 238000003756 stirring Methods 0.000 claims abstract description 5
- 238000001035 drying Methods 0.000 claims abstract description 3
- GQHWSLKNULCZGI-UHFFFAOYSA-N trifluoromethoxybenzene Chemical compound FC(F)(F)OC1=CC=CC=C1 GQHWSLKNULCZGI-UHFFFAOYSA-N 0.000 claims abstract 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- SELFZOLQRDPBKC-UHFFFAOYSA-N 1-chloro-4-(trifluoromethoxy)benzene Chemical compound FC(F)(F)OC1=CC=C(Cl)C=C1 SELFZOLQRDPBKC-UHFFFAOYSA-N 0.000 claims description 3
- RTUDBROGOZBBIC-UHFFFAOYSA-N 1-iodo-4-(trifluoromethoxy)benzene Chemical compound FC(F)(F)OC1=CC=C(I)C=C1 RTUDBROGOZBBIC-UHFFFAOYSA-N 0.000 claims description 3
- SEAOBYFQWJFORM-UHFFFAOYSA-N 1-bromo-4-(trifluoromethoxy)benzene Chemical compound FC(F)(F)OC1=CC=C(Br)C=C1 SEAOBYFQWJFORM-UHFFFAOYSA-N 0.000 claims description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 claims 2
- 239000007788 liquid Substances 0.000 claims 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- -1 carbamyl hydrazines Chemical class 0.000 description 3
- 239000005708 Sodium hypochlorite Substances 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 231100000004 severe toxicity Toxicity 0.000 description 2
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 2
- BBCXTYLYQSDZFP-UHFFFAOYSA-N 1-chloro-4-(trifluoromethoxy)benzene trifluoromethoxybenzene Chemical compound ClC1=CC=C(C=C1)OC(F)(F)F.FC(OC1=CC=CC=C1)(F)F BBCXTYLYQSDZFP-UHFFFAOYSA-N 0.000 description 1
- 241000723353 Chrysanthemum Species 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 108010052164 Sodium Channels Proteins 0.000 description 1
- 102000018674 Sodium Channels Human genes 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- ROMMVUMWISCVBE-UHFFFAOYSA-N [F].N#CC#N Chemical compound [F].N#CC#N ROMMVUMWISCVBE-UHFFFAOYSA-N 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000007857 hydrazones Chemical class 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 238000006303 photolysis reaction Methods 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 150000007659 semicarbazones Chemical class 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/06—Compounds containing any of the groups, e.g. semicarbazides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/06—Compounds containing any of the groups, e.g. semicarbazides
- C07C281/08—Compounds containing any of the groups, e.g. semicarbazides the other nitrogen atom being further doubly-bound to a carbon atom, e.g. semicarbazones
- C07C281/14—Compounds containing any of the groups, e.g. semicarbazides the other nitrogen atom being further doubly-bound to a carbon atom, e.g. semicarbazones the carbon atom being further bound to a carbon atom of a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810114496.3A CN108059606B (zh) | 2018-02-05 | 2018-02-05 | 一种利用尿素制备氰氟虫腙中间体的方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810114496.3A CN108059606B (zh) | 2018-02-05 | 2018-02-05 | 一种利用尿素制备氰氟虫腙中间体的方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN108059606A true CN108059606A (zh) | 2018-05-22 |
CN108059606B CN108059606B (zh) | 2020-03-27 |
Family
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Family Applications (1)
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CN201810114496.3A Active CN108059606B (zh) | 2018-02-05 | 2018-02-05 | 一种利用尿素制备氰氟虫腙中间体的方法 |
Country Status (1)
Country | Link |
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CN (1) | CN108059606B (zh) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0753501A (ja) * | 1993-08-17 | 1995-02-28 | Nissan Chem Ind Ltd | セミカルバゾン誘導体及び有害生物防除剤 |
CN101774951A (zh) * | 2010-01-29 | 2010-07-14 | 南开大学 | 一种氰氟虫腙合成方法 |
CN102584639A (zh) * | 2011-12-22 | 2012-07-18 | 山东京博控股股份有限公司 | 对三氟甲氧基苯胺基甲酰肼的合成方法 |
CN106928098A (zh) * | 2015-12-31 | 2017-07-07 | 江苏优嘉植物保护有限公司 | 一种茚虫威中间体缩胺基脲的合成方法 |
-
2018
- 2018-02-05 CN CN201810114496.3A patent/CN108059606B/zh active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0753501A (ja) * | 1993-08-17 | 1995-02-28 | Nissan Chem Ind Ltd | セミカルバゾン誘導体及び有害生物防除剤 |
CN101774951A (zh) * | 2010-01-29 | 2010-07-14 | 南开大学 | 一种氰氟虫腙合成方法 |
CN102584639A (zh) * | 2011-12-22 | 2012-07-18 | 山东京博控股股份有限公司 | 对三氟甲氧基苯胺基甲酰肼的合成方法 |
CN106928098A (zh) * | 2015-12-31 | 2017-07-07 | 江苏优嘉植物保护有限公司 | 一种茚虫威中间体缩胺基脲的合成方法 |
Non-Patent Citations (4)
Title |
---|
李洪侠等: ""对三氟甲氧基苯胺基甲酰肼的合成"", 《广东化工》 * |
王卫霞等: ""一种清洁高效的氰氟虫腙合成工艺研究"", 《江苏农业科学》 * |
白丽萍等: ""氰氟虫腙合成方法述评"", 《农药》 * |
陆阳等: ""新型杀虫剂氰氟虫腙的合成技术"", 《农药科学与管理》 * |
Also Published As
Publication number | Publication date |
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CN108059606B (zh) | 2020-03-27 |
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Effective date of registration: 20210119 Address after: Room 201, No.5, Lane 3399, Kangxin Road, Pudong New Area, Shanghai Patentee after: SHANGHAI LINKCHEM TECHNOLOGY Co.,Ltd. Address before: 225127 No. 199, Yang Hua Xi Road, Yangzhou, Jiangsu Patentee before: YANGZHOU POLYTECHNIC INSTITUTE |
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CP03 | Change of name, title or address | ||
CP03 | Change of name, title or address |
Address after: Room 201, No. 5, Lane 3399, Kangxin Road, Pudong New Area, Shanghai, 201318 Patentee after: Shanghai Lingkai Technology Co.,Ltd. Country or region after: China Address before: Room 201, No.5, Lane 3399, Kangxin Road, Pudong New Area, Shanghai Patentee before: SHANGHAI LINKCHEM TECHNOLOGY Co.,Ltd. Country or region before: China |