• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:

    公开号:SU999969A3
    申请号:SU813260552
    申请日:1981-03-04
    公开日:1983-02-23
    发明作者:Дюрр Дитер
    申请人:Циба-Гейги Аг (Фирма)；
    IPC主号:
    专利说明:

    Kie solvents such as low molecular weight alcohols, ketones, dimethylformamide or dimethyl sulfoxide, as well as water-immiscible chlorinated hydrocarbons, ethers or aromatic hydrocarbons. Compounds of formula I at high flow rates can be used as herbicides of total effect. However, it is more useful to use them at a flow rate of about 0.1 to 5 kg / ha as selective herbicides in cultivated plants when sprouted according to the post-rise method or in case of freshly harvested according to the pre-emergence method. So they inhibit or hinder the growth of weeds, first of all, sprouted double leaves, also many old plants, single-leaved species like Lolium, Alopecurus, Rottboellia, Sorghum, Digitaria, Setaria and Panicum. At the same time, cultivated plants, such as cereals, barley, wheat, rye, corn or rice, as well as others, such as cotton and soy, are completely or minimally at a consumption rate of 1 kg / ha. dessication and defoliation of cotton or potato crops shortly before harvesting. The usual consumption norms of a gerbshd according to the invention, per hectare fluctuate, a review of the activity of the used active substance, the standing of the soil, climatic and weather conditions, the type and time of use and the type of crop and weeds to be destroyed, between 0.1 and 10, 0 kg are preferably between 0.5 and 4.0 kg. In addition, the compounds of the formula T have a growth regulating effect: they inhibit the growth of plants. Examples of the effects exerted by the use of compounds, for example, are with a decrease in vegetative growth in soybean and similar leguminosities, which leads to an increase in the yield of this crop; inhibition of grass growth, c. goal of saving work on cutting; the inhibition of vegetative growth of cereals, which leads to plants with shorter, firmer stems that are not easily able to crawl under the influence of wind and weather. The compounds of formula 1 are stable compounds that are soluble in common organic solvents, such as alcohols, ethers, ketones, dimethylformamide, dimethyl sulfoxide. They are not explosive and corrosive and their use does not require special precautions. The agent is prepared by intensively mixing and grinding the active substances of the formula I with suitable carriers and / or dispersants, while adding antifoaming agents, wetting agents, dispersants and (or) solvents with respect to the active substances. Active Substances may be available. the following forms of processing in which they are applied. Solid forms of processing: pulverized preparation, preparation for soil application, granulated, granulated in a casing, impregnated granulated and homogeneous granulated. Water-dispersed active substance concentrates: wettable powder; pastes, emulsions, emulsion preparations. I Liquid forms of processing: solutions, dispersions. The concentrations of active principle in the agents are 1-80% by weight, but may be in lower concentrations, 0.05-1% by weight. Other biocidal active substances or agents may be admixed with the described agents. Thus, new agents, in addition to the compounds of formula 1 mentioned above, for expanding the spectrum of action may contain, for example, insecticides, fungicides, bactericides, fungicides, bacteriostatic agents, nematocides, or other herbicides. In the following example, the preparation of 1- (2-nitro-5-phenoxyphenyl) -2-oxazoline of formula I is described. Other properly prepared active substances are listed in tab. 1, Example. 2- (2-nitro-5- (2chloro-4-trifluoromethylphenoxy) phenyl 2-oxazrlin. Rast1or 184 g (0.05 mol) 2-nitro5- (2-z | op-4-t, rifluoromethylphenoxy) benzoyl chloride in 500 ml of toluene is added dropwise to a solution of 90 g of ethanolamine in 300 ml of dioxane at 20–40 ° C. After 3 hours p-oxyethyl amide of 2-nitro-5- (2-chloro-4-trifluoromethylphenoxy) benzoic acid is precipitated by adding ice water. After drying, 1.99 g (98% of theoretical) material is obtained with a mp of 142-143 ° C. 199 g of this oxyethylamide are mixed with 150 g of thionyl chloride and 400 ml of toluene and then kept at 4 ° C for 20 hours. solution of The residue is stirred in 500 MP of methylene chloride and 0.6 g of tetrabutylammonium chloride and then mixed with 42 g of powdered sodium hydroxide. Heat for 30 minutes with reverse reflux and stirred for a further 10 hours. For processing, the mixture is poured into water, the organic phase is separated. , washed, dried and evaporated to a dry residue. The residue remains the title compound as a transparent tint with a refractive index of 1.5703. Exit 109 g (79% of theoretical).
    Analysis: Calculated,% C 49.70, H 2.61, -N. 7.24.
    Found,% 1 C 49.5, H 2.6, N 7.1.
    Molecular weight 346.71. NMR spectrum corresponds to the structure.
    In a manner similar to this example, the following compounds are obtained, which are listed in Table 1, where the physical characteristics of the compounds of the formula T are given.
    Table 1
    2-yl. EXAMPLE 2. The processing of active substances - compounds of formula I into agricultural forms of use can be carried out, for example, according to one of the following prescriptions. 1. Granules t. To obtain a 5% granulate, the following substances are used: 5 parts 2 -2-nitro-5- (2-chloro-4 trifluoromethyl-phenoxy) phenyl 2-oxazoline; 0.25 parts of epoxidized vegetable oil; 0.25 h, cetiopoligly of the ether; 3.50 parts of polyethylene glycol; 91 hours kaolin (grain size 0.3-0.8 mm). The active substance is mixed with vegetable oil and dissolved in 6 parts of acetone, after which polyethylene glycol and cetyl polyglycol ether are added. Thus, the resulting vegetable, thief is sprayed onto the kaolin and then evaporated in vacuo. 2. Wetting powder. To obtain 70% and 10% wetted powder, the following constituents are used: Ov h, 2 -2-nitro-5- (2-chloro-4-trifluoromethyl-phenoxy) phenyl -2-oxazoline; 5 hours sodium
    T pl. 84 ° C tilnaftilsulfat; 3 hours of condensate. Naphthalene qyhl-acacids, phenolsulphonic acid and formaldehyde 3: 2: 1, Yu. H. Of kaolin} 12 hours. 10 h. Named active substance. Baj 3h. mixtures of sodium sulphates of saturated fatty alcohols; 5 parts of naphthalene sulfonic acid and formaldehyde condensate J 82 hours of kaolin. Said active substance is sprinkled with appropriate carriers (kaolin and chalk) and then mixed and milled with the remaining constituents. A wetted powder is obtained with excellent wettability and ability to be suspended. From such wetted pores, by diluting with water, suspensions of OD-8% of the active substance can be obtained, which are suitable for controlling weeds in plant cultures. 3. Concentrate emulsion. In order to obtain a 25% concentrated emulsion of the emulsion, they are mixed with each other .. 25 hours, 2- 2-NITRO-5- (2-chloro-4-trI111To-methylphenoxy) -phenyl -2-oxazoline; . mixtures of nonylphenol polyoxyethylene or calcium dodecylbenzene sulfate, 15 parts of cyclohexanone; 55 hours xylene. This concentrate may be diluted with water in an emulsion to suitable concentrations, for example, 0.1-10%. Such emulsions are suitable for controlling weeds in cultivated plants. 4. Pastes. The following substances are used to make a 45% paste; 45 parts of 2- 2-NITRO-5- (2-chloro-4-trifluoromethylphenoxy) 2-oxazoline 5 hours, sodium aluminosilicate, 14 hours, cetyl polyglycol ether with 8 mol of ethylene oxide} 1 part oleyl polyglycol ether with 5 mol of ethylene glycol; 2 h. Spun oil; 10 hours polyethylene glycol; 23 hours water 45 parts of 2- 2-nitro-5- (2-chloro-4-trifluoromethylphenoxy) -phenyl 2-oxazoline 5 parts of ethylene glycol; 3 h octylphenoxy polyethylene glycol with 9-10 mol of ethylene oxide per mol octylphenol; 3 parts of the mixture of aromatic sulfonic sulfonic acids condensed with the Form with an ice-hydroxide in the form of ammonium, 1 hour of silicone oil in the form of a 75% emulsion, 0.1 mixtures of 1- {3-chloroallyl) -3,5,7-triazo-adamantane-chloride with sodium carbonate, the chlorine value is a minimum of ll, 5% j 0.2 parts of a biopolymer concentrate with a maximum of 100 microbes per g 2 2., 7 hours of water. In a suitable device, the active substance is intensively smothered and ground with additives. A paste is obtained from which suspensions of any desired concentration can be obtained by diluting with water. In addition to compounds of the formula I, these forms of application can include, for example, insecticides, fungicides, fungistatic agents, bacteriostats, nematocides, or the cheapest herbicides to expand the spectrum of action. The active substance in suitable apparatus for this is intensively mixed and ground with additives. A paste is obtained from which suspensions with any desired concentration can be obtained by diluting with water. . Example 3. The coat of arms and the inhibiting growth of plants, the effect of the compounds of formula I is determined by the following experiments. Pre-emergence herbicidal action (pre-growing action), in a greenhouse, seeds of p & sthenium are sown in 12–15 cm flower pots so that 10–25 plants can grow on each pot. Immediately after sowing, the soil surface is treated with an aqueous suspension of the active substance obtained from a 10% wettable powder. Four different ranges of concentrations are used, corresponding to 2 and. 1 kg of active substance per 1 ha. Flower pots are kept in a greenhouse at 22-25 ° C and 50-70% of the relative humidity of the roses of the spirit and regular watering, and experience estimates-. with in 3 weeks. The condition of the plants is assessed according to the following EWRC-assessment scheme (European Weed Research Council): 9 - the plants succeed as untreated controls; 6-9 - light damage; 5 medium damage; - those yellow povrelgdeni; 1 - plants died. Compounds 1-4 were tested (Table 1). The results of tests for pre-emergence herbicidal action of representation, lena in the table .. 2. Table 2
    Herbicidal action when applying active substances after germination of plants (post-emergence).
    Various cultivated plants and weeds from seeds are grown in the greenhouses in the greenhouse until they reach the 4-6-th degree stage. The plants are then sprayed with aqueous emulsions of the active substances (obtained from a 25% strength concentration) in dosages of 2 and 1 kg / ha. Obra Continuation of the table. 2
    Plants that are harvested are maintained under the optimal conditions for cooling, regular irrigation at 22-25 ° C and 50-70% relative humidity of air. Evaluation | 1 experiment is carried out 15 days after processing on the so-called; 40 bathroom appraisal scheme. The results for compounds 2 and 4 (see table) are listed in Table. 3, which contains specific test results for
    post-harvest herbicidal action.
    I -. -.
    Table 3.
    Selective herbicidal effect on rice according to the post-emergence method.
    Rice plants cultivated for 25 days in a greenhouse in large rectangular cups. Seeds of weeds found in rice crops are then sown between rows of rice plants.
    The cups are well watered and kept at about 1 ° C and high humidity. After 12 days, when the weeds have sprung up and reached the 2-3-leaf stage, the ground
    Drying and defoliruyuschee action.
    Cotton plants of the Deltaptne variety were cultivated in clay pots in a greenhouse. Upon completion, form
    Continued tabl, 3
    in cups it is covered with a 2.5 cm high layer of water. Then the active substance is applied in the form of an emulsion concentrate with a pipette between rows of plants. The emulsion concentrate is diluted to apply in such a way that it corresponds in the field of application rates 1 and 1/2. kg of active food per hectare. The experience is assessed after 4 weeks. . The results for compounds 1 and 2 (see Table 1) are presented in Table. 4, where the results of tests of the post-emergence herbicidal action on fig.
    Table 4
    Neither the boxes are sprayed with aqueous preparations of the active substance 1 at a rate that would correspond to 1.2, 0.6 and 0.3 kg / ha in the field. Raw races
    权利要求:
    Claims (1)
    [1]
    Claim
    A method for producing 3-heterocyclic derivatives of 4-nitro-2'-chloro (or 2 ', 6'-dichloro) - 4' - trifluoromethyldiphenyl ethers of the formula D where R is hydrogen or chloro;
    X is oxygen or sulfur
    A-C ^ -C ^ is alkylene, agonium differs in that the compound of formula H where X, R and A have the indicated meanings, is treated with alkali metal hydroxide when boiled in an inert organic solvent.
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    同族专利:
    公开号 | 公开日
    ES8201401A1|1982-01-01|
    EP0035475A1|1981-09-09|
    PL229972A1|1981-11-13|
    ZA811425B|1982-03-31|
    CS225828B2|1984-02-13|
    AT5478T|1983-12-15|
    IL62279A|1984-09-30|
    PL126684B1|1983-08-31|
    IL62279D0|1981-05-20|
    ES500071A0|1982-01-01|
    JPS56154461A|1981-11-30|
    DD156664A5|1982-09-15|
    US4431439A|1984-02-14|
    AR227537A1|1982-11-15|
    DE3161525D1|1984-01-05|
    CA1161841A|1984-02-07|
    AU6806281A|1981-09-10|
    EP0035475B1|1983-11-30|
    US4350519A|1982-09-21|
    AU538588B2|1984-08-23|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US2786870A|1954-04-19|1957-03-26|Parke Davis & Co|Synthesis of chloramphenicol and related acylamidodiols|
    US3652645B1|1969-04-25|1984-07-24|
    US3563920A|1969-06-16|1971-02-16|Dow Chemical Co|Bi-2-oxazoline and oxazine ethers and thioethers|
    US3981905A|1970-03-16|1976-09-21|Boots Pure Drug Company Limited|2- propionic acids|
    US3877921A|1971-06-28|1975-04-15|Scott & Sons Co O M|Herbicidal Phenoxyalkyloxazolines|
    US3776961A|1971-12-23|1973-12-04|Oil Corp|3-substituted 4-nitrophenyl halophenyl ethers|
    US3928416A|1972-03-14|1975-12-23|Rohm & Haas|Herbicidal 4-trifluoromethyl-4{40 nitrodiphenyl ethers|
    US3816446A|1972-04-11|1974-06-11|Merck & Co Inc|-4-chlorobenzyl)heterocycles|
    US4019892A|1975-12-31|1977-04-26|Shell Oil Company|Herbicidal heterocyclic compounds|
    EP0002812B1|1978-01-02|1982-02-03|Ciba-Geigy Ag|Phenoxy-alkyl oxazolines, their preparation, compositions containing them and their application as herbicides|
    IL56484D0|1978-01-25|1979-03-12|Ciba Geigy Ag|Novel phenoxyalkyloxazolines, their preparation and their use as herbicides|US4576960A|1981-12-23|1986-03-18|Hoechst Roussel Pharmaceuticals Incorporated|6,11-Dihydro-11-oxo-dibenz[b,e]oxepin derivatives|
    US4515946A|1981-12-23|1985-05-07|Hoechst-Roussel Pharmaceuticals Inc.|6,11-Dihydro-11-oxo-dibenz-[b,e]oxepin derivatives|
    US4843087A|1983-08-29|1989-06-27|Sterling Drug Inc.|Di-heterocyclic compounds and their use as antiviral agents|
    AU634608B2|1989-12-09|1993-02-25|Kyoyu Agri Co., Ltd.|2-substituted phenyl-2-oxazoline or thiazoline derivatives, process for producing the same and insectides and acaricides containing the same|
    DE4404373A1|1994-02-11|1995-08-17|Bayer Ag|Substituted oxazacycloalkenes|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    CH173980|1980-03-05|
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