前苏联专利SU1032992A3 Method of destroying weed plants,bushes and aquaeous plants

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专利摘要:
Novel compounds represented by formula (I) or (II) are provided: <IMAGE> (I) <IMAGE> <IMAGE> (II). They can control annual and perennial weeds, shrubs and aquatic plants more effectively than their mother compounds, or (2-amino-4-methylphosphinobutyryl)alanylalanine and 2-amino-4-methylphosphinobutanoic acid, respectively.
公开号:SU1032992A3
申请号:SU792753552
申请日:1979-04-13
公开日:1983-07-30
发明作者:Такемацу Тецуо；Коннаи Макото；Сузуки Акира；Татибана Кунитака；Цуруока Такаси；Иноуе Сигехару；Ватанабе Тецуро
申请人:Мейдзи Сейка Кайся Лтд (Фирма)；
IPC主号:

专利说明:

: Yu
;ABOUT
:R
The invention relates to chemical IMC methods for controlling undesirable vegetation using phosphinic acid derivatives. A known method of combating undesirable vegetation is by treating it with N-phosphonomethylglycine (glyphosphate) p. V / Cl- (fH - ((
where R, OH or OMe, where Me is a cation of an organic or inorganic base;
Y is the anion of an inorganic or organic acid, m is 0; 1/2; 12,
However, this method is also not always effective. (SI) SNCO- {and where p is O or 1, in the amount of 0, 75 kg / ha. Compounds of formula (1} can be obtained by adding an equimolar amount of choline to an aqueous solution of a compound of formula O -Ci-donBH3-P-CHg-dHj where R is hydroxyl or alanylalanyl residue. It is recommended to use water liberated from carbon dioxide, since choline tends to form carbonate. The aqueous solution is then concentrated to dryness, the residue is dissolved in a 10-fold volume of a solvent, such as methanol or ethanol, adding a LO-50-fold volume of an organic solvent, such as ethyl acetate, chlorine. and benzene or diethyl ether, a white precipitate is obtained which is dried under vacuum in the presence of a drying agent to give a choline compound of the formula () in the form of a white powder. Choline. 2-amino- (oxy) (methyl) -phosphinoyl butyryl salt Alaninal The aim of the invention is to increase the effectiveness of the method.
This goal is achieved in that, according to the method of killing weeds, bushes and aquatic plants, the treatment is carried out with phosphine acid derivatives of general formula 2992.2 However, this method is not effective for broad-leaved weeds and bushes. The closest to the proposed 5 is a method of controlling undesirable vegetation, which consists in treating undesirable plants with phosphonic acid derivatives of the formula & CHj - P (HY) BI ((t) H-CH-CO) in Nina is designated as $ P-1295 choline, and the choline salt of 2-amino- (oxy) {methyl) phosphinoyl acid is designated as AMPB chooline, and substances 2-amino- (oxy) (methyl) phosphinoylbutyryl alanylalanine and 2-amino- (oxy) (methyl) phosphinoyl butyric acid - like, SF-1293 and AMPV, respectively. : The compounds of the formula (O have the physicochemical properties shown in Table 1. The substances prepared by the above-described treatment are the individual substances of the formula (1), which is confirmed by mass spectrometry and thin-layer xp method by atographic analysis. Shown that AMPB choline gives a protonated molecular ion peak (M + 1) at l / e-285 using the method of desorbing the field with mass chromatometry, confirms that AMPB choline is an individual substance. Further, AMPB choline gives a single spot with an Rf value of 0.3.1 in thin layer chromatography on cellulose C p fixator. For the manifestation, ethanol: water, ") when using spot detection reagents with ninhydrin and Draggendorf, which shows, is an individual compound. The compound AMPB and the compound containing AMPB give a color reaction with ingidrin, during which the blue-violet color develops, while compounds that do not contain AMPB do not produce this color reaction. Similarly, choline and substances containing choline ,. they give a color reaction with the Draggendorf reactor, in which a reddish-brown color develops, while AMPB does not produce this color reaction. Example 1. Choline L-AMPB. 3.55 g of L-AMPB solution in 0 ml of boiled and cooled water and 2.38 g of choline added to the mixture. The mixture is concentrated and the resulting residue is dissolved in 50 ml of ethanol. A white precipitate is isolated by adding 500 ml of ethyl acetate. The upper layer is discarded by decantation and the precipitate is washed with a small amount of ethyl acetate and dried under vacuum over phosphorus pentoxide to obtain g of choline AMPB in the form of a white powder, melting at. Found: C, 2.20; H V.ZZ; N 9.81; p 10.38. . C-10 H5tsN205P Calculated: C 42.25; H 8.86; N 9.85; R 10.90 EXAMPLE 2. Choline OL-AMPB. 7. 9 g of barium salt of DL-AMPB is dissolved in 25 ml of water and 1.52 g of choline sulfate is added. The precipitate of the barium sulphate formed is filtered off and the filtrate is condensed. The precipitate is dissolved in 25 ml of ethanol and a white precipitate is isolated by adding 250. ml of acetone. The upper layer is discarded by decantation. The precipitate is broken with a small amount of acetone and dried under vacuum over phosphorus pentoxide to obtain 2.75 g of choline DL-AMPB in the form of a white powder, melting at 152-157 ° C. NeidenD: C 42.18; H 8.82; N 9.79; Р 10.97 С «H25Nj, 05P is calculated: С 42.25; I am 8.86; N 9.85; P 10.90 Example 3. Choline SF-1293. 3.23 g of SF-1293 is dissolved in 25 m of boiled and cooled water and 1.21 g of choline is added. The mixture is concentrated and the residue is dissolved in 25 ml of methanol. A white precipitate was isolated by adding 50 ml of diethyl. The upper layer is discarded by decantation and the precipitate is washed with a small amount of diethyl ether and dried under vacuum over phosphorus pentoxide to obtain 4.26 g of choline, SF-1293 in the form of a white powder, melting at. Found: C 45.02; H N, 23; N 13.10; R 7.33. , . C 6Hs5N ,, OjP Calculated: С 45.07; H 8.27; N 13.14; P 7.26 To evaluate the results of experiments, use the following scale: Damage indicator. leaf destruction,% After 4 months after treatment, the reproduction inhibition effect is evaluated, which is defined as the degree of inhibition (in percent). . Test 1: Compounds according to the invention and other compounds used for comparison are diluted to a prescribed concentration and sprayed with natural weeds growing on them by spraying on the leaves in the amount of 150 liters per 10 a. 10 octylphenyl polyoxyethanol is added as a surfactant. The kill rate after 21 days and the effect of inhibiting reproduction after 2 months are determined. (Oigitaria adscendes, Echinochloa Crusgalli) and 4 months. (other weeds) The results are shown in Table 2. Test 2: The compounds according to the invention and the other compounds listed in Table 3 are diluted to the prescribed concentration and sprayed onto the bushes by spraying their leaves on a site planted with Japanese cypress in an amount of 150 liters per 10 a. After an incident of 30 days and 3 months, the destruction indicator is determined. Plant height, cm: dl
cypress 50-70, for chestnut about 50; for Sasa nipponica50-90, for Mischan.thus uinensis about 100, for Rubus crataegifolins 70-100.
The results are shown in table 3
Test 3- The compounds according to the invention and the other compounds listed in the table are diluted to the prescribed concentration and applied to the bushes growing under natural conditions by treating them in an amount of 150 liters per 10 a.
O / T octylphenylpropyl lyoxyethanol is added as a surfactant. The destruction rate after i 1 and 3 months and the effect of inhibiting reproduction after 3 months are determined.
Experience i. The baud is placed in plastic containers of 20x30 cm in size and liquid fertilizer is added to the water.
Two plants of Eichhornia crass Eye solms float in each tank. A 0.1-0.2% solution of bl-AMPB choline is added with 0.1 or p, 2% of each of the surfactants listed in Table 5. Each solution was sprayed onto the foliage in an amount of 100 liters per 10 a. The destruction rate was determined after 21 days and 3 months and the effect of reproduction inhibition after 3 months. The results are shown in table.5.
Test 5. Water is placed in a container made of plastic material with a size of 20x30 cm and liquid fertilizer is added. Two races are placed in each vessel: the shadows of Eichhorinla crassipes solms that float on the water. On the leaf
plants are applied in the amount of 1QO l per 10 ares 0.1 or 0, solutions of each of the compounds according to the invention and which are listed in Table 6.
0.1% octylphenylpolyoxyethanol was added as a surfactant. A kill rate was determined after 21. days and 3 months and a reproduction inhibition effect after 3 months. By; the results obtained are given in; tab. 6j
Experience 6. The soil from the rice floor is placed in square, with a side of 50 cm, pots of concrete. Plants of Sagtttaria trifolla L., Sagittaria pygmaea Mig, Hydrocharis dubia, Sagittaria Aginashi Makino are transplanted on this soil, after which water is poured into the soil at a height of -5 cm. Yes.
After a period of 1 month, compounds according to the invention are applied in an amount of 100 liters per 10 a, and the treatment is subjected to leaves; the concentration of the compounds is chosen in accordance with the prescribed dose.
0.1 octylphenium polyoxyethanol is used as a surfactant.
The kill rate after 21 days 3 months and the effect of reproduction inhibition after 3 months are determined.
The results are shown in table 7.
Thus, the proposed method for eliminating weeds, shrubs and aquatic plants is effective.
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1032992
2T T a b l and c a. 5 6.2% correspond to 1.0
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27. Note. Concentrations of 0.1 and 1, 0 and 2.0 kg / ha.
28
1032992 Continuation of table 6; 0.2% correspond to the amount

权利要求:
Claims (1)
[1]
METHOD FOR DESTROYING WEEDS, SHUSTERS AND AQUATIC PLANTS by treating them with the active principle based on derivatives of phosphinic acid, which is based on the fact that, in order to increase the efficiency of the method, the treatment is carried out with phosphinic acid derivatives of the general formula
9 <'Hj-P ^ H ^ CHCO-CNHCH-CO-NH-CH-COVOi.CH ^ NCHjCH ^ OH _ О' НЬЦ where η is 0 or 1, in the amount of 0.75 “3.75 kg / ha. Priority by signs: 04/15/78 the way to destroy sor-; _from nyak and bushes. 'S
04.07 · 78 a method of destruction of water I plants.
1 1032992. 2

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同族专利:

公开号 | 公开日

DE2915085A1|1979-10-25|

US4226610A|1980-10-07|

BR7902241A|1979-12-04|

IT7921898D0|1979-04-13|

ES480214A1|1980-01-16|

FR2422674A1|1979-11-09|

AU4586779A|1979-10-25|

AU526102B2|1982-12-16|

GB2018776A|1979-10-24|

MY8400304A|1984-12-31|

GB2018776B|1982-09-22|

DE2915085C2|1985-05-09|

CA1136644A|1982-11-30|

FR2422674B1|1985-01-11|

IT1120121B|1986-03-19|

引用文献:

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

US3832394A|1972-07-17|1974-08-27|Meiji Seika Kaisha|Methanephosphinylethane substituted amid trimer of alanine|

US3868407A|1973-11-21|1975-02-25|Monsanto Co|Carboxyalkyl esters of n-phosphonomethyl glycine|

DE2717440C2|1976-05-17|1984-04-05|Hoechst Ag, 6230 Frankfurt|Weed control with [ propyl-1] methylphosphinic acid derivatives|

CA1120280A|1977-11-08|1982-03-23|Makoto Konnai|Herbicidal compositions andherbicidal processes|

US4265654A|1977-12-28|1981-05-05|Meiji Seika Kaisha Ltd.|Herbicidal compositions|JPS5839127B2|1978-03-09|1983-08-27|Meiji Seika Co|

EP0010067B1|1978-10-05|1983-08-31|Ciba-Geigy Ag|Process for influencing plant growth|

DE3008186A1|1980-03-04|1981-10-15|Hoechst Ag, 6000 Frankfurt|SYNERGISTIC COMBINATIONS OF PHOSPHINOTHRICIN|

DE3035554A1|1980-09-20|1982-05-06|Hoechst Ag, 6000 Frankfurt|HERBICIDAL AGENTS|

US4466913A|1981-06-30|1984-08-21|Maiji Seika Kaisha Ltd.|Phosphorus-containing compounds and process for producing the same|

EP0075334A3|1981-09-25|1984-03-21|The Wellcome Foundation Limited|Pharmaceutical compounds, and preparation, formulations and use thereof|

JPH0373556B2|1983-05-27|1991-11-22|Meiji Seika Co|

ZW23187A1|1986-12-15|1988-06-29|Hoffmann La Roche|Phosphinic acid derivatives|

FR2650733A1|1989-08-08|1991-02-15|Roussel Uclaf|NEW PESTICIDE USES OF BIALAPHOS|

US6083874A|1997-11-11|2000-07-04|Elf Atochem North America, Inc.|Composition and method for plant desiccation|

法律状态:

优先权:

申请号 | 申请日 | 专利标题

JP4466278A|JPS6121960B2|1978-04-15|1978-04-15|

JP8048678A|JPS559003A|1978-07-04|1978-07-04|Herbicide for aquatic plant|

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