1,2-disubstituted ally/arylox yphthalate compounds and use thereof

A technology of aryloxybenzoic acid and di-substitution, applied in the field of aryloxybenzoic acid 1

Inactive Publication Date: 2006-03-22
DALIAN UNIV OF TECH
View PDF4 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But as shown in the present invention, aryloxybenzoic acid 1,2 disubstituted allyl ester compounds have not been disclosed

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • 1,2-disubstituted ally/arylox yphthalate compounds and use thereof
  • 1,2-disubstituted ally/arylox yphthalate compounds and use thereof
  • 1,2-disubstituted ally/arylox yphthalate compounds and use thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[0036] Example: Synthesis of 5-(2-chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoic acid 2-(methoxycarbonyl)-1-phenylallyl ester (compound 1) :

[0037]

[0038] Add III-1 (11.6 grams, 0.032 moles, available from the market) and 150 milliliters of methylene chloride in a 250-ml reaction flask, stir, add oxalyl chloride (6.1 grams, 0.048 moles), 2 drops of DMF, stir at room temperature for 5 hours, concentrated to obtain 11.0 g of acid chloride, the appearance of which was yellow liquid (IV-1).

[0039]

[0040] Add V-1 (0.58 grams, 3.0 mmoles) in the reaction bottle of 50 milliliters, triethylamine (0.46 grams), 5 milliliters of dichloromethanes, drip IV-1 (1.2 grams, 3.2 millimoles) under stirring cooling The mixed solution of 10 ml of dichloromethane was added in about half an hour, and the reaction was carried out at room temperature for 6 hours. After the reaction was completed, 100 ml of dichloromethane and 50 ml of water were added to the reaction liquid, and the...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The present invention belongs to the field of herbicide technology, and is especially 1, 2-disubstituted allyl aryloxy phthalate compounds and their application. The general expression of the compounds is shown. The compounds have herbicidal activity, especially on gramineous and broad-leaved weed, and may be used to control monocotylous weed effectively when it is applied before or after seeding emergence.

Description

technical field [0001] The invention belongs to the technical field of herbicides, and relates to a 1,2-disubstituted allyl ester compound of aryloxybenzoic acid and an application thereof. Background technique [0002] Because weeds develop resistance to herbicides or compositions thereof over time, there is a continuing need to invent new and improved herbicidal compounds and compositions. In addition, considering economical and environmental factors, it is also necessary to invent herbicides with different mechanisms of action from existing herbicides. [0003] Certain aryl formic acid compounds have been reported as herbicides (DE2311638, EP0020052). However, the aryloxybenzoic acid 1,2-disubstituted allyl ester compound shown in the present invention has not been disclosed. Contents of the invention [0004] The invention provides a 1,2-disubstituted allyl ester compound of aryloxybenzoic acid, as shown in general formula I: [0005] [0006] in: [0007] X is ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C07C205/59A01N39/00A01P13/00
Inventor 于春睿徐龙鹤崔东亮张弘吐松李斌
Owner DALIAN UNIV OF TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products