CN1927835A - Compound of 2-benzoxyacrylate and application thereof - Google Patents
Compound of 2-benzoxyacrylate and application thereof Download PDFInfo
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- CN1927835A CN1927835A CN 200510047154 CN200510047154A CN1927835A CN 1927835 A CN1927835 A CN 1927835A CN 200510047154 CN200510047154 CN 200510047154 CN 200510047154 A CN200510047154 A CN 200510047154A CN 1927835 A CN1927835 A CN 1927835A
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Abstract
The present invention discloses one kind of 2-benzoxy acrylate compound with general expression as shown. The compound of the present invention has excellent herbicidal activity and capacity of controlling broadleaf weeds effectively in seedling stage.
Description
Technical field
The invention belongs to the weedicide field.
Background technology
Because the succession of weeds population, transition and to the drug-fast generation of chemical pesticide with develop rapidly; people to the reinforcement of ecological environmental protection consciousness and to chemical pesticide pollute, agricultural chemicals is to non-target organism influence and the attention of home to return to problem in the agricultural chemicals ecotope; world cultivated area reduces and the population growth strengthens the grain demand amount; developing rapidly and reason such as updating of cropping system of agriculture production technology, need constantly invention novel with improved herbicidal compound and composition.
Some 2-benzoic acid acrylate compound is as the existing report of weedicide (USP6251829).But as the isoindole heterocyclic 2-benzoic acid acrylate compound that contains shown in the present is not seen open.
Summary of the invention
The invention provides a kind of 2-benzoic acid acrylate compound of novel structure, shown in general formula (I):
In the formula:
X is selected from H or halogen;
R
1Be selected from H or C
1-C
6Alkyl;
R
2Be selected from H or C
1-C
6Alkyl;
R
3Be selected from C
1-C
6Alkyl, C
3-C
6Thiazolinyl or C
3-C
6Alkynyl.
Comparatively preferred compound is among the present invention, in the general formula (I):
X is selected from H or F;
R
1Be selected from methyl;
R
2Be selected from methyl;
R
3Be selected from C
1-C
6Alkyl, C
3-C
6Thiazolinyl or C
3-C
6Alkynyl.
The alkyl of indication comprises the straight or branched alkyl in the general formula (I).Thiazolinyl is meant the straight or branched form, and the group of 1 to 2 carbon-carbon double bond is arranged, for example, and propenyl, allyl group etc.Alkynyl is meant the straight or branched form, and 1 to 2 carbon carbon triple-linked group is arranged, for example, and proyl, propargyl etc.
General formula compound of the present invention (I) can be prepared by following method:
With raw material (II can be buied by market) and SOCl
2, oxalyl chloride or PCl
3Be dissolved in The suitable solvent for example in chloroform, methylene dichloride, tetracol phenixin, normal hexane, benzene, toluene, ethyl acetate, tetrahydrofuran (THF) or the dioxane etc., and make catalyzer with organic bases such as triethylamine, pyridine or DMF etc., temperature is-10 ℃ reacted 0.5-48 hour under boiling point, made intermediate acyl chlorides (III).
Intermediate acyl chlorides (III) and 3-alkyl-2-oxo-carboxylicesters (with reference to the JP59-164749 preparation), in The suitable solvent, temperature is reacted down to boiling point and to be made intermediate (IV) in 0.5-48 hour for-10 ℃.Solvent can be selected from chloroform, methylene dichloride, tetracol phenixin, hexane, benzene, toluene, ethyl acetate, acetone, DMF, THF or dioxane etc.Add alkaloids, as triethylamine, pyridine, sodium hydroxide, potassium hydroxide, yellow soda ash, salt of wormwood, sodium bicarbonate etc. to reacting favourable.
Intermediate (V) can adopt conventional chemical reduction method preparation by intermediate (IV).As being reductive agent with zinc powder or iron powder etc., with water, ethanol, methyl alcohol, ethyl acetate, tetrahydrofuran (THF) or glacial acetic acid is solvent, add acidic substance such as ammonium chloride, hydrochloric acid or acetate etc. to reacting favourable, temperature was carried out reduction reaction for-10 ℃ in 0.5-48 hour to the following reaction of boiling point.
Intermediate (V) and 4,5,6,7-tetrahydrochysene isobenzofuran-1, the 3-diketone is dissolved in the The suitable solvent, for example glacial acetic acid, diacetyl oxide etc., temperature be 0 ℃ to boiling point down reaction made target compound (I) in 0.5-48 hour, add a small amount of alkaline matter in the reaction to reacting favourable, as triethylamine, pyridine or 4-Dimethylamino pyridine etc.
Part general formula of the present invention (I) compound sees Table 1.
Table 1: the The compounds of this invention of part shown in general formula (I)
| Compound | X | R 1 | R 2 | R 3 | Rerum natura |
| 1 | H | Methyl | Methyl | Methyl | Light yellow oil |
| 2 | H | Methyl | Methyl | Ethyl | Light yellow oil |
| 3 | H | Methyl | Methyl | Propyl group | Light yellow oil |
| 4 | H | Methyl | Methyl | Allyl group | Light yellow oil |
| 5 | H | Methyl | Methyl | Propargyl | Light yellow oil |
| 6 | F | Methyl | Methyl | Ethyl | White solid mp93-94 ℃ |
Compound in the table 1
1H NMR (CDCl
3, 300MHz) data are as follows:
Compound 1:8.087-8.077 (m, 1H), 7.560-7.546 (m, 2H), 3.769 (s, 3H), 2.457-2.429 (m, 4H), 2.417 (s, 3H), 1.900 (s, 3H), 1.851-1.822 (m, 4H)
Compound 2:8.071-8.062 (m, 1H), 7.557-7.540 (m, 2H), 4.229 (q, 2H), 2.457-2.430 (m, 4H), 2.344 (s, 3H), 1.898 (s, 3H), 1.852-1.812 (m, 4H), 1.272 (t, 3H)
Compound 3:8.086-8.076 (m, 1H), 7.555-7.541 (m, 2H), 4.132 (t, 2H), 2.454-2.427 (m, 4H), 2.275 (s, 3H), 1.898 (s, 3H), 1.849-1.809 (m, 4H), 1.698-1.628 (m, 2H), 0.898 (t, 3H)
Compound 4:8.076-8.069 (m, 1H), 7.555-7.547 (m, 2H), 5.961-5.870 (m, 1H), 5.268 (dd, 2H), 4.684 (d, 2H), 2.454-2.414 (m, 4H), 2.281 (s, 3H), 2.043 (s, 3H), 1.909-1.821 (m, 4H)
Compound 5:8.082-8.074 (m, 1H), 7.557-7.539 (m, 2H), 4.762 (s, 2H), 2.450-2.414 (m, 5H), 2.291 (s, 3H), 1.921 (s, 3H), 1.849-1.820 (m, 4H)
Compound 6:7.999 (d, 1H), 7.392 (d, 1H), 4.215 (q, 2H), 2.45 (m, 4H), 2.267 (s, 3H), 1.855 (s, 3H), 1.83 (m, 4H), 1.255 (t, 3H)
General formula of the present invention (I) compound has excellent weeding activity, uses behind seedling and can effectively control broadleaf weeds.
The present invention comprises that also with general formula (I) compound be the herbicidal composition of active ingredient.The weight percentage of active ingredient is 1-99% in this herbicidal composition.Comprise also in this herbicidal composition that agricultural goes up acceptable carrier.
Herbicidal composition of the present invention can several formulations form use.Usually with compound dissolution of the present invention or be scattered in and be mixed with preparation in the carrier so that be easier to disperse when using as weedicide.For example: can general formula of the present invention (I) compound be processed into multiple formulation for example wettable powder or missible oil etc. according to ordinary method.Therefore, in these compositions, contain acceptable liquid or solid carrier on a kind of agricultural at least.Usually also need to add suitable tensio-active agent in the composition.
Other embodiments of the present invention are method of controlling weeds, and this method comprises herbicidal composition of the present invention is imposed on the surface of the place of described weeds or described weed growth or its growth medium.Usually the comparatively suitable effective dose of selecting is that per hectare 1 restrains 1000 grams, and preferred effective dose is that per hectare 10 restrains 500 grams.Use for some, can in herbicidal composition of the present invention, add one or more other weedicide, can produce additional advantage and effect thus.
Compound of the present invention both can use separately also can be mixed together use with other known sterilant, sterilant, plant-growth regulator or fertilizer etc.
Should be clear and definite be in claim of the present invention institute restricted portion, can carry out various conversion and change.
Embodiment
The following example and living test are tested the result and be can be used to further specify the present invention, but do not mean that restriction the present invention.
Synthetic example
Example 1: compound 2 synthetic
In 250 milliliters reaction flask, add 2-chloro-5-nitrobenzoic acid (11.69 grams, 58.00 mmole) and 150 milliliters of methylene dichloride, stir and slowly add oxalyl chloride (11.00 grams down, 87.00 mmole), add 3 DMF again, stirring at room reaction 4 hours, afterwards, methylene dichloride and excessive oxalyl chloride are deviate from decompression, get 12.00 gram yellow liquid, i.e. intermediate acyl chlorides.
In 500 milliliters reaction flask, add 3-methyl-2-ketobutyric acid ethyl ester (4.60 grams, 32.00 mmole), triethylamine (3.80 grams, 38.00 mmole) and in 50 milliliters of dichloromethane solutions, be added dropwise to above-mentioned intermediate acyl chlorides (7.50 grams under the ice-water bath, 34.00 mmole) and the solution that form of 100 milliliters of methylene dichloride, drip half an hour approximately.Reaction is after 5 hours under the room temperature, in reaction solution, add 200 milliliters of ethyl acetate and 200 ml waters, ethyl acetate layer is used saturated sodium bicarbonate aqueous solution, each 200 milliliters of washing of saturated sodium-chloride water solution successively, anhydrous magnesium sulfate drying, the decompression precipitation, separate (ethyl acetate/petroleum ether=1/10) through silica gel column chromatography, get the faint yellow oily thing of 8.50 grams, be the intermediate esters of unsaturated carboxylic acids.
In 250 milliliters the reaction flask, add intermediate esters of unsaturated carboxylic acids (8.50 grams, 26.00 mmoles), ammonium chloride (13.89 grams, 260.00 mmoles), 50 milliliters in water, 50 milliliters of tetrahydrofuran (THF)s under the room temperature, stirring and dissolving is warmed up to about 50 ℃.Zinc powder (15.21 grams, 234 mmoles) is slowly joined (about 30 minutes) in the said mixture between 50-60 ℃, reaction is 4 hours about 60 ℃.Remove by filter insolubles, the filtrate layering, oil reservoir washing, concentrate 7.85 gram left and right sides reddish-brown semisolids, be intermediate amine.Crude product washs with 1: 5 ethyl acetate/petroleum ether, obtains the yellow solids of 6.50 grams.
4.
In 150 milliliters the reaction flask, add 70 milliliters of intermediate amine (6.55 grams, 22.00 mmoles), tetrahydrophthalic anhydride (3.8 grams, 24.20 mmoles), acetic acid, 90 ℃ of reactions 6 hours.Deviate from whole solvents, separate (ethyl acetate/petroleum ether=1/10) through silica gel column chromatography, get the yellow thickness oily target compound of 5.50 grams, promptly compound 2.
Example 2: compound 5 synthetic
In 250 milliliters reaction flask, add 3-methyl-2-ketobutyric acid sodium salt (2.76 grams, 20.00 mmole), propargyl bromide (3.57 grams, 30.00 mmole), N, 30 milliliters of dinethylformamides, stirring and dissolving is warmed up to about 40 ℃ and reacted 3 hours, afterwards, in reaction solution, add 50 milliliters of ethyl acetate and 50 ml waters, layering, upper strata be 2 * 20 milliliters, 20 milliliters saturated sodium bicarbonate aqueous solutions of water, 20 milliliters of saturated sodium-chloride water solution washings successively, anhydrous magnesium sulfate drying, the decompression precipitation obtains 2.60 gram 3-methyl-2-ketobutyric acid alkynes propyl ester.
In 250 milliliters reaction flask, add above-mentioned carboxylicesters (2.30 grams, 14.90 mmole), 20 milliliters of methylene dichloride, triethylamine (1.81 grams, 17.88 mmole), be added dropwise to 2-chloro-5-nitrobenzoyl chloride (3.61 grams under the ice-water bath, 16.41 mmole) and the solution that form of 10 milliliters of methylene dichloride,, drip half an hour approximately, reaction is after 5 hours under the room temperature, in reaction solution, add 50 ml waters, organic phase is water successively, saturated sodium bicarbonate aqueous solution, each 50 milliliters of washing of saturated sodium-chloride water solution, anhydrous magnesium sulfate drying, decompression precipitation, get the faint yellow oily thing of 5.82 grams, be the intermediate benzoyloxy unsaturated carboxylate.
In 250 milliliters reaction flask, add benzoyloxy unsaturated carboxylate (4.83 grams, 14.31 mmoles), iron powder (3.21 grams, 57.24 mmoles), 50 milliliters of glacial acetic acids stir, and are heated to about 60 ℃ and react 2 hours.Not tolerant back precipitation is removed in cooling, obtains 4.73 gram intermediate amine.
In 150 milliliters the reaction flask, add 50 milliliters of intermediate amine (4.00 grams, 13.00 mmoles), tetrahydrophthalic anhydride (2.18 grams, 14.30 mmoles), acetate, 90 ℃ of reactions 6 hours.Deviate from whole solvents, separate (ethyl acetate/petroleum ether=1/10) through silica gel column chromatography, get the yellow thickness oily target compound of 2.91 grams, promptly compound 5.
Other compounds in the table 1 can make by above similar method.
Give birth to and survey example
Example 3: with the former medicine of acetone solution,, join in the certain water gaging that contains tensio-active agent, make certain density preparation by design dosage.Spray with mobile belt atomizer.The examination material is put in spraying rolling in the cupboard and is with, and mobile shower nozzle is sprayed onto medicament on the examination material with the covering of the fan Sprayable through examination material top, identical on nozzle and the common field spray device.Roll band and will try material and shift out outside the cupboard, place loft drier dry.
Test behind the seedling, seed germination also grew 10-21 days, made the examination material that has a series of growing stages before the processing, selected size, the consistent examination material of growing stage then, handled, and handled to be placed on the greenhouse and to water.The examination material with compound treatment does not compare.The examination material is monocotyledon weed barnyard grass grass, lady's-grass, broadleaf weed youth-and-old-age, piemarker.
Examination material after the spraying drying places the greenhouse.Test is poured water from the bottom and was kept 48 hours so that water does not touch the blade face behind the seedling.
Handle the preventive effect of periodical visual inspection investigation reagent agent in back, and investigate various weeds.Inhibiting rate is total effect of various infringements such as chlorosis, withered spot, retarded growth or the calcination of leaf angle, obtains the result with blank after relatively.Partial test the results are shown in Table 2.
Table 2: the weeding activity of part general formula (I) compound (behind the seedling, inhibiting rate %)
| Dosage gram effective constituent/hectare | The barnyard grass grass | Lady's-grass | Youth-and-old-age | Piemarker | |
| Compound 1 | 20 | 20 | 60 | 100 | 100 |
| Compound 2 | 20 | 20 | 55 | 95 | 100 |
| Compound 3 | 20 | 45 | 50 | 100 | 100 |
| Compound 4 | 20 | 40 | 50 | 100 | 100 |
| Compound 5 | 20 | 55 | 75 | 100 | 100 |
| Compound 6 | 15 | --* | -- | -- | 90 |
*: "--" expression is not surveyed.
Claims (5)
1, a kind of 2-benzoic acid acrylate compound, shown in general formula (I):
Wherein:
X is selected from H or halogen;
R
1Be selected from H or C
1-C
6Alkyl;
R
2Be selected from H or C
1-C
6Alkyl;
R
3Be selected from C
1-C
6Alkyl, C
3-C
6Thiazolinyl or C
3-C
6Alkynyl.
2, compound as claimed in claim 1 is characterized in that, in:
X is selected from H or F;
R
1Be selected from methyl;
R
2Be selected from methyl;
R
3Be selected from C
1-C
6Alkyl, C
3-C
6Thiazolinyl or C
3-C
6Alkynyl.
3, the described compound of claim 1 is used to control the purposes of weeds.
4, a kind of herbicidal composition contains general formula as claimed in claim 1 (I) compound and agricultural goes up acceptable carrier, and the weight percentage of active ingredient is 1-99% in the composition.
5, a kind of control method for weed is characterized in that: the herbicidal composition as claimed in claim 4 of using the weeding effective dose on the growth mediums of weeds or weeds or place.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100471547A CN100427466C (en) | 2005-09-08 | 2005-09-08 | Compound of 2-benzoxyacrylate and application thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100471547A CN100427466C (en) | 2005-09-08 | 2005-09-08 | Compound of 2-benzoxyacrylate and application thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1927835A true CN1927835A (en) | 2007-03-14 |
| CN100427466C CN100427466C (en) | 2008-10-22 |
Family
ID=37857989
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2005100471547A Expired - Fee Related CN100427466C (en) | 2005-09-08 | 2005-09-08 | Compound of 2-benzoxyacrylate and application thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100427466C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009046665A1 (en) * | 2007-10-09 | 2009-04-16 | Sinochem Corporation | Isoindole compounds and their uses |
| CN101407490B (en) * | 2007-10-09 | 2012-01-25 | 中国中化股份有限公司 | 3-benzoxy acrylic ester compounds and uses thereof |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU542544B2 (en) * | 1980-03-12 | 1985-02-28 | Nippon Kayaku Kabushiki Kaisha | Tetrahydrophthalimide derivatives |
| JPS60109563A (en) * | 1983-11-16 | 1985-06-15 | Kanesho Kk | Herbicide |
| JPS6345253A (en) * | 1986-08-13 | 1988-02-26 | Nippon Soda Co Ltd | Isoindole derivative, production thereof and selective herbicide |
| US4919704A (en) * | 1987-08-14 | 1990-04-24 | Ciba-Geigy Corporation | 4,5,6,7-Tetrahydroisoindole-1,3-diones |
| US6251829B1 (en) * | 2000-04-18 | 2001-06-26 | Rohm And Haas Company | Herbicidal benzoyloxy carboxylates and carboxamides |
-
2005
- 2005-09-08 CN CNB2005100471547A patent/CN100427466C/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009046665A1 (en) * | 2007-10-09 | 2009-04-16 | Sinochem Corporation | Isoindole compounds and their uses |
| CN101407490B (en) * | 2007-10-09 | 2012-01-25 | 中国中化股份有限公司 | 3-benzoxy acrylic ester compounds and uses thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100427466C (en) | 2008-10-22 |
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Granted publication date: 20081022 Termination date: 20130908 |