CS262441B2 - Herbicide na base derivatives of diphenylethere and process for preparing active component - Google Patents
Herbicide na base derivatives of diphenylethere and process for preparing active component Download PDFInfo
- Publication number
- CS262441B2 CS262441B2 CS866512A CS651286A CS262441B2 CS 262441 B2 CS262441 B2 CS 262441B2 CS 866512 A CS866512 A CS 866512A CS 651286 A CS651286 A CS 651286A CS 262441 B2 CS262441 B2 CS 262441B2
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- Czechoslovakia
- Prior art keywords
- formula
- compound
- hydrogen
- active ingredient
- atom
- Prior art date
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- 230000002363 herbicidal effect Effects 0.000 title claims description 22
- 239000004009 herbicide Substances 0.000 title description 4
- 238000004519 manufacturing process Methods 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 55
- 239000000203 mixture Substances 0.000 claims description 37
- 239000004480 active ingredient Substances 0.000 claims description 19
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 125000005843 halogen group Chemical group 0.000 claims description 8
- BGOZIOZETMDSAQ-UHFFFAOYSA-N 3-phenoxy-3h-2-benzofuran-1-one Chemical class C12=CC=CC=C2C(=O)OC1OC1=CC=CC=C1 BGOZIOZETMDSAQ-UHFFFAOYSA-N 0.000 claims description 7
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- 239000000460 chlorine Substances 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
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- 125000002524 organometallic group Chemical group 0.000 claims description 4
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000004426 flaxseed Nutrition 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- OVEHNNQXLPJPPL-UHFFFAOYSA-N lithium;n-propan-2-ylpropan-2-amine Chemical compound [Li].CC(C)NC(C)C OVEHNNQXLPJPPL-UHFFFAOYSA-N 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 235000012243 magnesium silicates Nutrition 0.000 description 1
- LWLPYZUDBNFNAH-UHFFFAOYSA-M magnesium;butane;bromide Chemical compound [Mg+2].[Br-].CCC[CH2-] LWLPYZUDBNFNAH-UHFFFAOYSA-M 0.000 description 1
- NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 description 1
- FRIJBUGBVQZNTB-UHFFFAOYSA-M magnesium;ethane;bromide Chemical compound [Mg+2].[Br-].[CH2-]C FRIJBUGBVQZNTB-UHFFFAOYSA-M 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- NCFSDGWPAKOPOU-UHFFFAOYSA-N n-ethylethanamine;lithium Chemical compound [Li].CCNCC NCFSDGWPAKOPOU-UHFFFAOYSA-N 0.000 description 1
- UYYCVBASZNFFRX-UHFFFAOYSA-N n-propan-2-ylcyclohexanamine Chemical compound CC(C)NC1CCCCC1 UYYCVBASZNFFRX-UHFFFAOYSA-N 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 150000002901 organomagnesium compounds Chemical class 0.000 description 1
- 125000002734 organomagnesium group Chemical group 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 235000011197 perejil Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 102220047090 rs6152 Human genes 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- CGRKYEALWSRNJS-UHFFFAOYSA-N sodium;2-methylbutan-2-olate Chemical compound [Na+].CCC(C)(C)[O-] CGRKYEALWSRNJS-UHFFFAOYSA-N 0.000 description 1
- UJTRRNALUYKHQE-UHFFFAOYSA-N sodium;diphenylmethylbenzene Chemical compound [Na+].C1=CC=CC=C1[C-](C=1C=CC=CC=1)C1=CC=CC=C1 UJTRRNALUYKHQE-UHFFFAOYSA-N 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000002426 superphosphate Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/87—Benzo [c] furans; Hydrogenated benzo [c] furans
- C07D307/88—Benzo [c] furans; Hydrogenated benzo [c] furans with one oxygen atom directly attached in position 1 or 3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Indole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB858522528A GB8522528D0 (en) | 1985-09-11 | 1985-09-11 | Diphenyl ether herbicides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS651286A2 CS651286A2 (en) | 1988-07-15 |
| CS262441B2 true CS262441B2 (en) | 1989-03-14 |
Family
ID=10585027
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS866512A CS262441B2 (en) | 1985-09-11 | 1986-09-09 | Herbicide na base derivatives of diphenylethere and process for preparing active component |
Country Status (24)
| Country | Link |
|---|---|
| EP (1) | EP0219144B1 (da) |
| JP (1) | JPH0678332B2 (da) |
| KR (1) | KR940009531B1 (da) |
| CN (1) | CN1017895B (da) |
| AT (1) | ATE48996T1 (da) |
| AU (1) | AU590793B2 (da) |
| BR (1) | BR8604300A (da) |
| CA (1) | CA1327810C (da) |
| CS (1) | CS262441B2 (da) |
| DE (1) | DE3667788D1 (da) |
| DK (1) | DK164908C (da) |
| ES (1) | ES2001670A6 (da) |
| FI (1) | FI863625L (da) |
| GB (1) | GB8522528D0 (da) |
| GR (1) | GR862306B (da) |
| HU (1) | HUT42425A (da) |
| IL (1) | IL79987A0 (da) |
| MA (1) | MA20766A1 (da) |
| NZ (1) | NZ217508A (da) |
| OA (1) | OA08409A (da) |
| PH (1) | PH23124A (da) |
| PT (1) | PT83333B (da) |
| ZA (1) | ZA866845B (da) |
| ZW (1) | ZW18586A1 (da) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2182328B (en) * | 1985-10-29 | 1989-09-20 | Shell Int Research | Diphenyl ether derivatives |
| US4911754A (en) * | 1987-07-16 | 1990-03-27 | American Cyanamid Company | Herbicidally active aryloxy saturated 5-membered benzo fused hetero-cyclic compounds |
| GB8720509D0 (en) * | 1987-09-01 | 1987-10-07 | Shell Int Research | Diphenyl ether herbicides |
| GB8720511D0 (en) * | 1987-09-01 | 1987-10-07 | Shell Int Research | Preparing diphenyl ethers |
| GB8722968D0 (en) * | 1987-09-30 | 1987-11-04 | Shell Int Research | Preparing diphenyl ethers |
| DE19809420A1 (de) | 1998-03-05 | 1999-09-09 | Basf Ag | Verfahren zur Herstellung von hochreinen Lithiumsalzen |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8332268D0 (en) * | 1983-12-02 | 1984-01-11 | Shell Int Research | Herbicides |
| EP0145078B1 (en) * | 1983-12-02 | 1988-10-12 | Shell Internationale Researchmaatschappij B.V. | Diphenyl ether herbicides |
| GB8625106D0 (en) * | 1986-10-20 | 1986-11-26 | Shell Int Research | Diphenyl ether herbicides |
| GB8720509D0 (en) * | 1987-09-01 | 1987-10-07 | Shell Int Research | Diphenyl ether herbicides |
-
1985
- 1985-09-11 GB GB858522528A patent/GB8522528D0/en active Pending
-
1986
- 1986-08-15 EP EP86201428A patent/EP0219144B1/en not_active Expired
- 1986-08-15 AT AT86201428T patent/ATE48996T1/de not_active IP Right Cessation
- 1986-08-15 DE DE8686201428T patent/DE3667788D1/de not_active Expired - Lifetime
- 1986-08-18 CA CA000516131A patent/CA1327810C/en not_active Expired - Fee Related
- 1986-09-09 CS CS866512A patent/CS262441B2/cs unknown
- 1986-09-09 ZW ZW185/86A patent/ZW18586A1/xx unknown
- 1986-09-09 IL IL79987A patent/IL79987A0/xx unknown
- 1986-09-09 FI FI863625A patent/FI863625L/fi not_active IP Right Cessation
- 1986-09-09 GR GR862306A patent/GR862306B/el unknown
- 1986-09-09 CN CN86105328A patent/CN1017895B/zh not_active Expired
- 1986-09-09 HU HU863892A patent/HUT42425A/hu unknown
- 1986-09-09 DK DK430586A patent/DK164908C/da not_active IP Right Cessation
- 1986-09-09 PT PT83333A patent/PT83333B/pt unknown
- 1986-09-09 JP JP61210847A patent/JPH0678332B2/ja not_active Expired - Fee Related
- 1986-09-09 ES ES8601705A patent/ES2001670A6/es not_active Expired
- 1986-09-09 KR KR1019860007561A patent/KR940009531B1/ko not_active Expired - Fee Related
- 1986-09-09 ZA ZA866845A patent/ZA866845B/xx unknown
- 1986-09-09 MA MA20994A patent/MA20766A1/fr unknown
- 1986-09-09 NZ NZ217508A patent/NZ217508A/xx unknown
- 1986-09-09 BR BR8604300A patent/BR8604300A/pt not_active IP Right Cessation
- 1986-09-09 AU AU62481/86A patent/AU590793B2/en not_active Ceased
- 1986-09-09 PH PH34238A patent/PH23124A/en unknown
- 1986-09-09 OA OA58949A patent/OA08409A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZW18586A1 (en) | 1987-08-12 |
| KR940009531B1 (ko) | 1994-10-14 |
| FI863625A7 (fi) | 1987-03-12 |
| PT83333A (pt) | 1986-10-01 |
| NZ217508A (en) | 1988-09-29 |
| DK430586D0 (da) | 1986-09-09 |
| OA08409A (en) | 1988-06-30 |
| CN86105328A (zh) | 1988-05-11 |
| PH23124A (en) | 1989-05-05 |
| IL79987A0 (en) | 1986-12-31 |
| CS651286A2 (en) | 1988-07-15 |
| CA1327810C (en) | 1994-03-15 |
| DK430586A (da) | 1987-03-12 |
| DK164908B (da) | 1992-09-07 |
| CN1017895B (zh) | 1992-08-19 |
| ZA866845B (en) | 1987-04-29 |
| EP0219144A1 (en) | 1987-04-22 |
| GR862306B (en) | 1987-01-02 |
| DE3667788D1 (de) | 1990-02-01 |
| FI863625L (fi) | 1987-03-12 |
| JPH0678332B2 (ja) | 1994-10-05 |
| EP0219144B1 (en) | 1989-12-27 |
| AU590793B2 (en) | 1989-11-16 |
| MA20766A1 (fr) | 1987-04-01 |
| PT83333B (en) | 1988-01-11 |
| JPS6261973A (ja) | 1987-03-18 |
| ES2001670A6 (es) | 1988-06-01 |
| GB8522528D0 (en) | 1985-10-16 |
| ATE48996T1 (de) | 1990-01-15 |
| FI863625A0 (fi) | 1986-09-09 |
| BR8604300A (pt) | 1987-05-05 |
| KR870003087A (ko) | 1987-04-15 |
| HUT42425A (en) | 1987-07-28 |
| AU6248186A (en) | 1987-03-12 |
| DK164908C (da) | 1993-01-25 |
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