专利摘要:
1. A method of controlling weeds in crops of cultivated plants by treating them or the soil on which they are prone to growth, with a herbicide derived from chloroacetanilide of the general formula (D) 1 .X CH2 - B Cd where RR is methyl, ethyl J is hydrogen, methyl; X is hydrogen, methyl, methoxy, chlorine, characterized in that, in order to increase the selectivity of action, the treatment is carried out with a mixture of a pro-, derived chloroacetanilide of the general formula
公开号:SU1101173A3
申请号:SU813228096
申请日:1981-01-09
公开日:1984-06-30
发明作者:Эйкен Карл;Рор Вольфганг;Иоахим Пандер Ханс;Вюрцер Бруно
申请人:Басф Аг (Фирма);
IPC主号:
专利说明:

CH3 1. CH2-X I
characterized in that, in order to increase the selectivity of the action, the treatment is carried out with a mixture of the chloroacetanilide derivative of formula V
with a 1,3-oxazine derivative of formula VI
SShSNz g | G-CCNS1,
V o
when the mass ratio of compounds V: VI is 1: P, equal to 1: 0.125-1, in the amount of 1.125-2.5 kg / ha.
The invention relates to chemical methods of controlling weeds in crops of cultivated plants by treating them with a herbicide and an antidote. We know how to control weeds ij, according to which substituted chloroacetanilides of the general formula CH7-A are used as a herbicide, where R R A is methyl or ethyl hydrogen or methylJ. substituted in the corresponding methyl, methox group or chlorine pyrazolyl, 1,2,4-triazolyl or 2, D-dimethylpyrrolyl. However, when using this herbicide in effective doses, crop plants are often damaged, i.e., the selectivity of the herbicide is not sufficient. The aim of the invention is to increase the selectivity of the method of weed control. This goal is achieved in that, according to the method for controlling weeds, plants are treated with a mixture of a derivative of chloroacetanilide of the general formula CH3 methyl, ethyl; hydrogen, methyl hydrogen, methyl, methoxy, chlorine, with 1,3-oxazine bottom of the general formula 3 SIRN; L --СНС12 hydrogen, methyl, hydrogen, methyl, ethyl, propyl, 1-ethyl-n-pentyl, or the ratio of compounds is 1: 0.125-1, in the amount of kg / ha, according to the second varioba treatment is carried out with a mixture of chlorine acetanilide formula j. one of 1,3-oxazine formulas CH3 CH% - sleep g I II H about
-BUT

4-Methoxypyrazolyl-1 Ethyl
D E F 3-Methylpyrazolyl-1, 4-Dimethylpyrrolyl-1 Me Teel
94
Butter
126 PRI me R 1. Experiments in greenhouse conditions. Plasticate boxes for seedlings with a length of 51 cm, a width of 32 cm and a height of 6 cm are filled with sand mixed with clay with a pH of 6 and a humus content of about 1.5%. In this substrate there is a wide range of maize or wheat. Besides; iToro, they are added .J as unwanted leafberry plants and foxtail. Unsterilized land additionally contains. viable weeds that increase the population of unwanted plants. Thus, the arable land is sown with the sowing of cultivated plants, which is clogged with weeds. Active substances and antidotes are introduced both in pure form and in the described mixtures. To do this, they are distributed in water in the form of an emulsion or suspension (water serves as a carrier) and sprayed by means of a thin-layer device onto the ground immediately after sowing and before the emergence of seedlings of experimental plants. In some cases, the herbicidal agent is also introduced into the ground before sowing. After sowing and processing, the crates are irrigated with water and covered with a transparent plastic cover until seeding the shoots. These measures ensure uniform germination and germination of plants. Yav (incubator at 18-30 C. Observation is carried out until corn develops into a phase of 3-5 leaves (after this stage the herbicidal agent does not act, which is also confirmed by experiments conducted in open ground). Evaluation of the average action is carried out on a scale from 0 to 100. At the same time, O means normal germination and development of plants in comparison with untreated and control plants, 100 corresponds to complete suppression of germination or dying of plants. At the same time, it is learned that, for example, in corn and even under completely normal conditions, and without any chemical treatment, individual plants appear ugly or repressed. Example 2. Field experiments. Open field experiments were carried out on small experimental sandy soil with pH 5-6 and humus content.1-1.5%. Pre-emergence treatment is carried out either immediately after sowing, or no later than three days after sowing of cultivated plants. The weed flora is represented by various species compositions of natural populations (only the dominant Do). The active substances and antidotes, as well as their mixtures, are suspended or emulsified in water (carrier and distribution to the medium) and the experienced units are treated with the help of a tractor mounted sprayer. With a lack of natural precipitation, additional watering is carried out to ensure the normal growth of cultivated plants and weeds. All experiments were carried out for several months so that the development of cultivated plants could be observed until the formation of seeds. The assessment of the average action of the herbicidal agent is also carried out on a scale from 0 to 100. Table 3-6 shows the results of the pre-emergence treatment (Table 3 and the experience in the greenhouse).
Table 3 Herbicide Antidote Active, kg / ha 54.0 64.0 74.0 Herbicide Antidote Active,
1.0 2.0 4.0
1.0 + 0.125 1.0 + 0.5 1.0 + 2.0 1.0 2.0
1.0 + 0.25 2.0 + 0.5 2.0 + 2.0 1.0 2.0 1.0 + 0.25
88 90 10 10 О 5
100
100
ABOUT
100
100
100
70 88 O 5 5
100
100
100
100
100
30 70 O
100
100
100 Continued from table 3 Damage,% Cultural ras-Sorn to shade Shchetinnik Millet pekukuruzatushe OOO O00 O00 Table4 Damage,% ha Cultivated Weeds ki Plants Petunier millet Maize
Antidote
Active herb Herbicide, kg / ha
1.0 + 1.0
2.0 + 0.25
2.0 + 2.0
1.0
2.0
1.0 + 0.25

1 + 1
2.0 + 0.5
2.0 + 2.0
1.0
2.0

1.0 + 0.25
2.0 + 0.5
1.0
2.0
.1.0 + 1.0
1.0 + 0.25
2.0 + 2.0
1.0
2.0
1.0 + 0.125
1.0 + 1.0
2.0 + 0.5
2.0
Damage,%
Sorn ki
{Cultivated plants
Petusia millet
Corn
100
100 ;
100
100
100
100
100
100
100
100
100
100
100
100
100 .
100
100
100
99
100
98
98
98
9b
15
“The data presented in the tables show that the new antagonist-acting 1,3-oxazines, introduced separately, have no effect or have a barely noticeable effect on the germination and growth of crops.
1101173 Table 6
however, the phytotoxicity of herbicidal acetanilides of formula 1 is significantly reduced (or completely eliminated) with respect to cultivated plants, such as corn and cereals.
权利要求:
Claims (3)
[1]
1. A method of controlling weeds in crops of cultivated plants by treating them or the soil on which they grow with a chloroacetanilide derivative of the general formula (I)> <n—
R 1 'where R' is hydrogen, methyl;
R is hydrogen, methyl, ethyl, propyl, 1-ethyl-n-pentyl, with a mass ratio of 1: P equal to 1: 0.125-
[2]
2 in the amount of 1.125-4 kg / ha <2. The method of controlling weeds in crops of cultivated plants by treating them with a herbicide - a derivative of chloroacetanilide of the formula III
ССН 2 С1 о
characterized in that, with increasing selectivity, de-processing is carried out with a mixture of where R R *
X about l the purpose of the action of the chloroacetanilide formula III with a derivative of 1,3-oxazine formula IV
CH 3 ^ CH 2 Cl
0 ethyl;
methyl;' methyl methoxy
- methyl
- hydrogen
- hydrogen, chlorine, and especially for increasing the selectivity of actions
C & SNE
V 0 th with the fact that, for the sake of purpose, the treatment is carried out with a mixture of prog of chloroacetanilide of general formula (I) with a derivative of 1,3-oxazine of general formula (U) in a weight ratio of compounds of formula (11: 11 /, equal to 1: 0.25-1, in the amount of 1.25-4 kg / ha.
[3]
3. A method of controlling weeds in crops of cultivated plants, by treating them with a herbicide derivative of chlorac ^ tanilide of the formula V unit
CH3 ch 2 --n (| Mt
ССН 2 С1 о
with a 1,3-oxazine derivative of the formula VI, characterized in that, in order to increase the selectivity of the action, the treatment is carried out with a mixture of the chloroacetanilide derivative of the formula V at a mass ratio of compounds V: VI 1: p equal to 1: 0.125-1, in an amount of 1.125- 2.5 kg / ha.
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同族专利:
公开号 | 公开日
AT66T|1981-05-15|
HU181851B|1983-11-28|
ES482839A1|1980-04-16|
AU4920979A|1980-01-31|
AU525577B2|1982-11-11|
CA1133902A|1982-10-19|
US4295875A|1981-10-20|
RO76976A|1981-08-30|
PL121169B2|1982-04-30|
AR230274A1|1984-03-01|
DE2832890A1|1980-02-14|
ZA793862B|1980-08-27|
BR7904768A|1980-04-22|
EP0007588A1|1980-02-06|
NZ191129A|1981-10-19|
IL57800A|1982-08-31|
DD145052A5|1980-11-19|
GR66644B|1981-04-03|
IL57800D0|1979-11-30|
PT69976A|1979-08-01|
EP0007588B1|1981-05-13|
PL217380A2|1980-04-21|
DE2960349D1|1981-08-20|
JPS5520768A|1980-02-14|
MA18536A1|1980-04-01|
CS213391B2|1982-04-09|
DK314979A|1980-01-28|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题

US3719466A|1970-04-16|1973-03-06|Gulf Research Development Co|Protection of wheat and grain sorghum from herbicidal injury|
CA1174865A|1971-04-16|1984-09-25|Ferenc M. Pallos|Thiolcarbamate herbicides containing nitrogencontaining antidote|
US4021224A|1971-12-09|1977-05-03|Stauffer Chemical Company|Herbicide compositions|
FR2137005B1|1971-05-11|1974-08-23|Delalande Sa|
US3989503A|1972-10-13|1976-11-02|Stauffer Chemical Company|Herbicidal antidote compositions with substituted oxazolidines and thiazolidines|
CH574207A5|1973-01-25|1976-04-15|Ciba Geigy Ag|
FR2310348B1|1975-05-07|1978-06-09|Ugine Kuhlmann|
DE2648008C3|1976-10-23|1980-09-04|Basf Ag, 6700 Ludwigshafen|Acetanilide|DE2948535A1|1979-12-03|1981-06-25|Basf Ag, 6700 Ludwigshafen|DICHLORACETAMIDES, HERBICIDE AGENTS THAT CONTAIN ACETANILIDES AS HERBICIDAL ACTIVE SUBSTANCES AND THESE DICHLORACETAMIDES AS AN ANTAGONISTIC AGENTS, AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH|
DE3119077A1|1981-05-14|1982-12-02|Basf Ag, 6700 Ludwigshafen|HETEROCYCLIC DIHALOGEN ACETMIDES, METHOD FOR THE PRODUCTION THEREOF AND HERBICIDAL AGENTS THAT CONTAIN ACETANILIDES AS HERBICIDAL ACTIVE SUBSTANCES AND THESE DIHALOGEN ACETAMINES AS AN ANTAGONISTIC AGENTS|
US4618361A|1983-12-12|1986-10-21|Ciba-Geigy Corporation|Acylamides and compositions for the protection of cultivated plants against the phytotoxic action of herbicides|
US4601745A|1983-12-12|1986-07-22|Ciba-Geigy Corporation|Composition for the protection of cultivated plants against the phytotoxic action of herbicides|
US5514678A|1992-03-26|1996-05-07|E. I. Du Pont De Nemours And Company|Arthropodicidal 1,2,4-triazinyl amides|
法律状态:
优先权:
申请号 | 申请日 | 专利标题
DE19782832890|DE2832890A1|1978-07-27|1978-07-27|HERBICIDAL AGENTS|
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