Herbicidic agent

专利摘要:
New and valuable substituted O-[aminosulfonyl]-glycolic anilides and a process for controlling the growth of unwanted plants with these compounds.
公开号:SU708977A3
申请号:SU731870088
申请日:1973-01-11
公开日:1980-01-05
发明作者:Фишер Адольф；Хампрехт Герхард；Мангольд Дитрих；Рор Вольфганг
申请人:Басф Аг (Фирма)；
IPC主号:

专利说明:

I
The invention relates to chemical agents for controlling weeds and undesirable vegetation, and is a herbicidal agent containing an active ingredient from the group of glycolic acid derivatives and flooded components from among liquid or solid carriers, surfactants, etc.
Herbicidal agents based on glycolic acid derivatives are known. These include, for example, the agent on. based on substituted amides of alkylsulfonyl glycolic acids; 11 The effectiveness of this agent is manifested at a dose of the active substance of 22.4 kg / ha.
Herbicidal agents are also known, the active substances of which are L-substituted halide acetic anilides. They are effective at a dose of 5.65 kg / ha. 2 However, known products of this type are not sufficiently effective for certain types of weeds.
The aim of the invention is to obtain a new herbicidal agent based on glycolic derivatives.
acid, blast: o1tsego increased herbicidal activity.
This goal is achieved by using a glycolic acid derivative of the general formula as an active ingredient of the herbicidal agent.
ОВ2
ten
K-Wi - $ - oCH2C-T
(h;
about
about
and
where R is alkyl or propargyl; R is alkyl, allyl, butenyl or butynyl.
The content of the active substance in the herbicide tool is 0.1-95 wt.%.
The forms of application of the active substances are common: solutions, emulsions, pastes, powders, etc. They are prepared by well-known techniques.
The effectiveness of the agent according to the invention is manifested when it is used both in the pre-emergence and in the post-emergence period.
The compounds of general formula (1) are obtained by reacting a substituted glycolic anilide anion with the substitution of aminosulfonyl chloride in the presence of a hydrogen chloride acceptor
Compounds of the general formula (1) are presented in the table.
Example 1. Pre-emergence treatment. Seeds of experimental plants
were sown in prepared soil and then treated with its preparative forms with active cich substances at the rate of 500 l / ha for the preparation (aqueous dispersion) and 2 kg / ha for the active substance. The evaluation of the experiment was carried out after 4-5 weeks of growing the plant {in the greenhouse according to the following scale:
O - no effect
l60- - full of death plants.
The results of the experiment are presented in table 2. The numbers of the compounds correspond to the numbers in table.1.
Example 2. Post-harvest processing (field experiment).
Experimental plants grown to a certain stage of development (from 2 to 14 cm) were treated with active substance preparative forms at the rate of 2 kg / ha for the active substance. Evaluation of effectiveness was carried out after 3-4 weeks after treatment.
Ikala evaluation is similar to example 1 (from about to 100).
The results of the experiment are presented in table.3.
In both experiments, the well-known herbicide, N-isopropylanilide chloroxy acid (compound A), was used for comparison.
Example 3. Dov descents and
treatment. The experiment was carried out under the conditions of Example 1. The soil is clay-sand. The dose is 1) their substances - 2 kg / ha. The rating scale is the same (from O
 to 100), the results of the experiment are presented in table 4,
.Example 4. Post-harvest processing (in greenhouse)
Experimental plants grown to 5–2–16 cm were treated with preparative forms of active substances at the rate of 1 kg / ha. The evaluation was performed on the same scale / cm, example 1/3 weeks after treatment, the results are presented in table.5.
Example 5. Post-harvest application (field experiment)
The conditions of the experiment are similar to example 21, dose 1.5 kg / ha. The results are presented in Table 6.
Example 6. Post-emergence 25ЕЕ521 13 (in greenhouse conditions)
. The experiment was carried out analogously to example 4, a dose of 1 kg / ha. The results of the experiment are presented in table.7.
Example 7, Dovskhodovka processing (in greenhouse conditions)
The experiment was carried out analogously to example 1, a dose of 2 kg / ha. The results of the experiment in table.8.
Example 8. Post-emergence treatment under greenhouse conditions.
The experiment was carried out analogously to example 4, the Dose of active substances
1kg / ha The results are shown in Table. 9.
PRI m e D 9, Dovskhodova processing in conditions of greenhouse
(similar to example 1).
The dose of the active substance 2kg / ha.
The results are presented in table 10. An example. 0. Sending a scrapbook about a scourge of botanists (cc example 4),
The dose of the active substance 1 kg / ha.
The results of the experiment are presented in table 10.
Table
N-butyn-1-Il-3-anilide onyl) glycolic acid; N-butyn-1-yl-3-anilide of glycolic acid; N-butene-1-yl-3-anilide-onyl) glycolic acid N-methyl. isoprop of colic acid of l-butyn-1-yl-3-anilide of okolic acid (isopropylaminosulfo (propylaminosulphonyl) (ieopropylaminosulphoylaminosulphonyl) gluc (methylaminosulphonyl) gly- (6 7 8 9 10 11 12
Experimental plants
Corn
Zoo mantle
With
Beet
The yearbook
Cloris
Millet
Elezina
M tlick
Continuation of table 1
The effectiveness of the active substance
(known)
compound 1 A
About 15
15 10
60 40 50 30 15 N-ethyleneilide o- (isopropylaminosulfonyl) glycolic acid N-ethyleneyl o- (ethylaminosulfonyl) glycolic acid N-butin-1-yl-3-anilide o- (ethylaminosulfonyl) glycolic acid, N-isopropylanilide o- ( ethylaminosulphonyl) glycolic acid N-isopropylanilide of o- (methylaminosulphonyl) glycolic acid N-methylanilide of o- (ethylaminosulphonyl) glycolic acid N-allylanilide of o- (methylaminosulphonyl) glycolic acid "MKBfl". - Dovskhodov treatment in greenhouse conditions / dose of 2 kg / ha Experienced plants substances Corn ... OO So ... OO Cotton ... OO Beet ... OO Hedgehog ... 9570 Bristle ... 9570 M tlic .. 9540 Koster ... 9540 Foxtail .... Post-emergence treatment (field trial), dose 2 kg / ha 2 Table2 Efficacy of active compound No. 1 compound l Table 3
Table
eleven
Oh oh
to
about
about
95 90
95
708977 .12
Continuation of table.8
Table 9
Table 10
LTD
90 90
13

权利要求:
Claims (2)
[1]
Invention Formula
A herbicidal agent containing a glycolic acid derivative as an active substance, as well as auxiliary components selected from
K-NH-S-OCHzt-Tf
J
propargyl;
where K „- alkyl With / -C ™ or R | -
alkyl, allyl, b tenil
or butynyl, in an amount of from 0.1 to 95% by weight.
Sources of information taken into account in the examination
70897714
Continuation of table 10
groups of liquid or solid surfactant carriers, differing in that
the purpose of enhancing herbicidal activity, it contains a glycolic acid derivative of the general formula
R
ABOUT
l. US Patent No. 3586721, Cl. 26025 293.4, published. 10.27.70 (prototype).
[2]
2. US patent No. 3475157, CL.71118, published.28.10.69.
thirty

类似技术:

---

公开号 | 公开日 | 专利标题

---

SU710499A3|1980-01-15|Herbicidic substance

---

SU708977A3|1980-01-05|Herbicidic agent

---

SU518107A3|1976-06-15|Herbicidal composition

---

US3884671A|1975-05-20|Herbicidal n-haloacyl | oxazolidines

---

SU670194A3|1979-06-25|Herbicide

---

US2863754A|1958-12-09|Method of weed control

---

SU667099A3|1979-06-05|Herbicide

---

SU563893A3|1977-06-30|Herbicide compound

---

SU651645A3|1979-03-05|Herbicide composition

---

US4018801A|1977-04-19|Substituted oxirane compounds

---

SU579847A3|1977-11-05|Herbicide

---

SU629851A3|1978-10-25|Method of fighting unwanted plant growth

---

SU577933A3|1977-10-25|Herbicide

---

US2893855A|1959-07-07|N-1-napthylchlorophthalamic herbicides

---

US3707366A|1972-12-26|Pre-emergent chemical method of combating unwanted vegetation

---

SU670196A3|1979-06-25|Herbicide

---

US3881908A|1975-05-06|Herbicidal N-haloacyl | oxazolidines

---

SU580801A3|1977-11-15|Herbicide

---

SU651644A3|1979-03-05|Herbicide

---

SU540551A3|1976-12-25|Herbicidal composition

---

SU843696A3|1981-06-30|Herbicidic composition

---

SU579845A3|1977-11-05|Herbicide

---

SU648049A3|1979-02-15|Herbicide

---

SU605520A3|1978-04-30|Herbicide

---

US3532686A|1970-10-06|Alkyleneiminourea compounds

同族专利:

---

公开号 | 公开日

---

DE2201432C2|1983-11-03|

---

IL41216A|1976-02-29|

---

GB1407114A|1975-09-24|

---

TR17278A|1975-03-24|

---

CS192459B2|1979-08-31|

---

FR2168009B1|1976-08-27|

---

JPS4880727A|1973-10-29|

---

AT322276B|1975-05-12|

---

CA1001642A|1976-12-14|

---

AU5080073A|1974-07-11|

---

IL41216D0|1973-03-30|

---

BG22788A3|1977-04-20|

---

HU165488B|1974-09-28|

---

FR2168009A1|1973-08-24|

---

JPS5635162B2|1981-08-15|

---

CH575712A5|1976-05-31|

---

IT976809B|1974-09-10|

---

PL78984B1|1975-06-30|

---

AU472352B2|1976-05-20|

---

OA04316A|1980-01-15|

---

ZA73264B|1973-11-28|

---

AR195814A1|1973-11-09|

---

BR7300284D0|1973-09-25|

---

NL7300422A|1973-07-17|

---

US3870740A|1975-03-11|

---

DK134042B|1976-09-06|

---

DD104171A5|1974-03-05|

---

DE2201432A1|1973-07-19|

---

BE794013A|1973-07-12|

---

DK134042C|1977-02-07|

---

BR7300274D0|1973-09-25|

引用文献:

---

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

---

---

US3536721A|1963-09-13|1970-10-27|Stauffer Chemical Co|Substituted-sulfonyl glycolamide compositions|DE2417764A1|1974-04-11|1975-10-30|Basf Ag|O-AMINOSULFONYL GLYCOLIC ANILIDES|

---

DE2431582A1|1974-07-01|1976-01-22|Basf Ag|O-AMINOSULFONYL-GLYCOLIC ACID AMIDE|

---

DE2453908A1|1974-11-14|1976-05-26|Basf Ag|HERBICIDAL MIXTURES|

---

US4144048A|1974-11-18|1979-03-13|Basf Aktiengesellschaft|Herbicidal compositions|

---

US4209317A|1974-11-18|1980-06-24|Basf Aktiengesellschaft|Herbicidal compositions|

---

DE2458972A1|1974-12-13|1976-06-16|Basf Ag|SUBSTITUTED O-ALKYL SULFONYL GLYCOLIC ANILIDES|

---

US4264520A|1974-12-13|1981-04-28|Basf Aktiengesellschaft|Substituted O-alkylsulfonylglycolic acid anilides|

---

DE2852274A1|1978-12-02|1980-06-19|Basf Ag|METHOD FOR PRODUCING SULFAMID ACID HALOGENIDES|

---

JPS611020B2|1978-12-28|1986-01-13|Hokko Chem Ind Co|

---

DE2904490A1|1979-02-07|1980-08-21|Bayer Ag|METHOD FOR THE PRODUCTION OF ALPHA HYDROXYCARBONIC ACID AMIDES|

---

DE3038598A1|1980-10-13|1982-05-19|Bayer Ag, 5090 Leverkusen|Alpha-hydroxy-carboxylic acid amide prepn. - by reacting an alpha formyl:oxy-n benzyloxy-carboxylic acid amide with an alcohol|

---

DE19504225A1|1995-02-09|1996-08-14|Hoechst Ag|Process for the preparation of O-acyloxycarboxylic acid anilides|

---

DE19933936A1|1999-07-20|2001-01-25|Bayer Ag|Substituted heteroaryloxyacetanilides|

法律状态:

优先权:

---

申请号 | 申请日 | 专利标题

---

DE2201432A|DE2201432C2|1972-01-13|1972-01-13|Substituted 0- [aminosulfonyl] -glycolic acid anilides and herbicides containing them|

---