KR900006761B1 - 벤조일페닐우레아의 제조방법 - Google Patents
벤조일페닐우레아의 제조방법 Download PDFInfo
- Publication number
- KR900006761B1 KR900006761B1 KR1019850007614A KR850007614A KR900006761B1 KR 900006761 B1 KR900006761 B1 KR 900006761B1 KR 1019850007614 A KR1019850007614 A KR 1019850007614A KR 850007614 A KR850007614 A KR 850007614A KR 900006761 B1 KR900006761 B1 KR 900006761B1
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- South Korea
- Prior art keywords
- formula
- compound
- fluorine
- chlorine
- compounds
- 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.)
- Expired
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- 238000002360 preparation method Methods 0.000 title description 8
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- PWPJGUXAGUPAHP-UHFFFAOYSA-N lufenuron Chemical compound C1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=CC(Cl)=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F PWPJGUXAGUPAHP-UHFFFAOYSA-N 0.000 description 1
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- IKHINJVRKROJSR-UHFFFAOYSA-N n-(2,5-dichloro-4-hydroxyphenyl)acetamide Chemical compound CC(=O)NC1=CC(Cl)=C(O)C=C1Cl IKHINJVRKROJSR-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
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- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- 150000002892 organic cations Chemical class 0.000 description 1
- 231100000194 ovacidal Toxicity 0.000 description 1
- 230000003151 ovacidal effect Effects 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
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- 230000000704 physical effect Effects 0.000 description 1
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- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
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- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
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- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
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- 239000000741 silica gel Substances 0.000 description 1
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- 125000005624 silicic acid group Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 235000013322 soy milk Nutrition 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical class CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Substances C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- PDSVZUAJOIQXRK-UHFFFAOYSA-N trimethyl(octadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)C PDSVZUAJOIQXRK-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C275/30—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by halogen atoms, or by nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C265/00—Derivatives of isocyanic acid
- C07C265/12—Derivatives of isocyanic acid having isocyanate groups bound to carbon atoms of six-membered aromatic rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C275/32—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
- C07C275/48—Y being a hydrogen or a carbon atom
- C07C275/54—Y being a carbon atom of a six-membered aromatic ring, e.g. benzoylureas
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH4993/84-1 | 1984-10-18 | ||
| CH?4993/84-1 | 1984-10-18 | ||
| CH499384 | 1984-10-18 | ||
| CH5361/84-2 | 1984-11-08 | ||
| CH536184 | 1984-11-08 | ||
| CH2048/85-1 | 1985-05-14 | ||
| CH204885 | 1985-05-14 | ||
| CH3502/85-2 | 1985-08-14 | ||
| CH350285 | 1985-08-14 | ||
| CH3502/85-2? | 1985-08-14 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR860003206A KR860003206A (ko) | 1986-05-21 |
| KR900006761B1 true KR900006761B1 (ko) | 1990-09-21 |
Family
ID=27428360
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019850007614A Expired KR900006761B1 (ko) | 1984-10-18 | 1985-10-16 | 벤조일페닐우레아의 제조방법 |
Country Status (18)
| Country | Link |
|---|---|
| US (3) | US4798837A (https=) |
| EP (1) | EP0179022B1 (https=) |
| JP (1) | JPH0347159A (https=) |
| KR (1) | KR900006761B1 (https=) |
| AU (1) | AU586194B2 (https=) |
| BG (1) | BG60408B2 (https=) |
| BR (1) | BR8505181A (https=) |
| CA (1) | CA1242455A (https=) |
| CY (1) | CY1548A (https=) |
| DE (1) | DE3580444D1 (https=) |
| DK (3) | DK160870C (https=) |
| ES (1) | ES8609221A1 (https=) |
| GB (3) | GB2165846B (https=) |
| IL (1) | IL76708A (https=) |
| LV (1) | LV10769B (https=) |
| MY (2) | MY102685A (https=) |
| NL (1) | NL930085I2 (https=) |
| TR (1) | TR22452A (https=) |
Families Citing this family (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5135953A (en) * | 1984-12-28 | 1992-08-04 | Ciba-Geigy | Use of acyl urea compounds for controlling endoparasites and ectoparasites of warm-blooded animals |
| IT1201456B (it) * | 1985-08-22 | 1989-02-02 | Donegani Guido Ist | "n-(2,6-difluorobenzoil)-n'3,5-dicloro-4-(3,3,3-trifluoro-2-cloroprop-1-en-1-il)fenil urea ad attivita' insetticida |
| US5288756A (en) * | 1985-10-14 | 1994-02-22 | Ciba-Geigy Corporation | Benzoylphenylureas |
| EP0219460B1 (de) * | 1985-10-14 | 1991-05-02 | Ciba-Geigy Ag | Benzoylphenylharnstoffe |
| EP0221847A3 (de) * | 1985-10-29 | 1988-03-23 | Ciba-Geigy Ag | Salze von Benzoylharnstoffen |
| ATE69603T1 (de) * | 1986-02-28 | 1991-12-15 | Ciba Geigy Ag | N-benzoyl-n'-phenylharnstoffe, ihre herstellung und verwendung bei der kontrolle von schaedlingen. |
| DE3613062A1 (de) * | 1986-04-18 | 1987-10-29 | Hoechst Ag | N-benzoyl-n'-phenyl(thio)harnstoffe, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel |
| US5177110A (en) * | 1989-10-27 | 1993-01-05 | Ciba-Geigy Corporation | Injectable parasiticidal composition |
| AU631259B2 (en) * | 1989-12-18 | 1992-11-19 | Ciba-Geigy Ag | Formulations of benzoylphenyl ureas for combating ectoparasites |
| US5403814A (en) * | 1991-03-25 | 1995-04-04 | Ciba-Geigy Corporation | Sulfonylureas |
| WO1995016354A1 (en) * | 1993-12-15 | 1995-06-22 | Ciba-Geigy Ag | Method of combating termites and other wood destructive insects |
| EP2260707A3 (en) * | 1994-06-08 | 2013-07-24 | Syngenta Participations AG. | Synergistic compositions comprising lufenuron |
| CH687732A5 (de) * | 1994-06-09 | 1997-02-14 | Ciba Geigy Ag | Verfahren zur Bekaempfung von Insekten. |
| US6323377B1 (en) | 1995-06-07 | 2001-11-27 | Syngenta Participations Ag | Oxidation process |
| US6040345A (en) * | 1996-11-08 | 2000-03-21 | Dow Agrosciences Llc | Benzoylphenylurea insecticides and methods of using them to control cockroaches |
| US5886221A (en) | 1997-11-03 | 1999-03-23 | Dow Agrosciences Llc | Benzoylphenylurea insecticides and methods of using certain benzoylphenylureas to control cockroaches, ants, fleas, and termites |
| AU5159898A (en) * | 1996-11-08 | 1998-05-29 | Dowelanco Llc | New benzoylphenylurea insecticides and methods of using certain benzoylphenylureas to control cockroaches, ants, fleas, and termites |
| DE19702207A1 (de) | 1997-01-23 | 1998-07-30 | Bayer Ag | Verfahren zur Herstellung von p-Haloalkoxyanilinen |
| DE69724659T2 (de) * | 1997-04-17 | 2004-03-25 | Syngenta Participations Ag | Verfahren zur hydroxylierung von 1,4-dichlorbenzol |
| US5811461A (en) * | 1997-10-31 | 1998-09-22 | Dow Agrosciences Llc | Benzoylphenylurea insecticides and methods of using them to control cockroaches, ants, fleas, and termites |
| US6844339B2 (en) * | 1998-01-16 | 2005-01-18 | Syngenta Crop Protection, Inc. | Use of neonicotinoids in pest control |
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1985
- 1985-10-14 EP EP85810468A patent/EP0179022B1/de not_active Expired - Lifetime
- 1985-10-14 IL IL76708A patent/IL76708A/xx not_active IP Right Cessation
- 1985-10-14 DE DE8585810468T patent/DE3580444D1/de not_active Expired - Lifetime
- 1985-10-16 TR TR34655/86A patent/TR22452A/xx unknown
- 1985-10-16 CA CA000493029A patent/CA1242455A/en not_active Expired
- 1985-10-16 GB GB08525516A patent/GB2165846B/en not_active Expired
- 1985-10-16 KR KR1019850007614A patent/KR900006761B1/ko not_active Expired
- 1985-10-17 AU AU48818/85A patent/AU586194B2/en not_active Expired
- 1985-10-17 BR BR8505181A patent/BR8505181A/pt not_active IP Right Cessation
- 1985-10-17 ES ES547951A patent/ES8609221A1/es not_active Expired
- 1985-10-17 DK DK476585A patent/DK160870C/da not_active IP Right Cessation
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1987
- 1987-06-04 US US07/058,631 patent/US4798837A/en not_active Expired - Lifetime
- 1987-08-10 MY MYPI87001269A patent/MY102685A/en unknown
- 1987-10-15 GB GB08724216A patent/GB2195635B/en not_active Expired
- 1987-10-15 GB GB08724215A patent/GB2195336B/en not_active Expired
-
1988
- 1988-10-24 US US07/262,121 patent/US4980506A/en not_active Expired - Lifetime
-
1990
- 1990-03-12 JP JP2060891A patent/JPH0347159A/ja active Granted
- 1990-10-15 US US07/597,656 patent/US5107017A/en not_active Expired - Lifetime
- 1990-11-07 DK DK266990A patent/DK164850C/da not_active IP Right Cessation
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1991
- 1991-03-22 CY CY1548A patent/CY1548A/en unknown
- 1991-08-09 DK DK144891A patent/DK164854C/da not_active IP Right Cessation
- 1991-12-17 MY MYPI91002333A patent/MY108591A/en unknown
-
1992
- 1992-06-15 BG BG096477A patent/BG60408B2/bg unknown
-
1993
- 1993-06-11 LV LVP-93-559A patent/LV10769B/en unknown
- 1993-06-22 NL NL930085C patent/NL930085I2/nl unknown
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