LU84914A1 - Alcoylamino n-phenyl pyrazole et n-phenyl pyrazole lactames herbicides - Google Patents

Info

Publication number

LU84914A1

LU84914A1 LU84914A LU84914A LU84914A1 LU 84914 A1 LU84914 A1 LU 84914A1 LU 84914 A LU84914 A LU 84914A LU 84914 A LU84914 A LU 84914A LU 84914 A1 LU84914 A1 LU 84914A1

Authority

LU

Luxembourg

Prior art keywords

group

carbon atoms

linear

general formula

branched

Prior art date

1982-07-15

Links

• Espacenet
• Global Dossier
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• WITMXBRCQWOZPX-UHFFFAOYSA-N 1-phenylpyrazole Chemical compound C1=CC=NN1C1=CC=CC=C1 WITMXBRCQWOZPX-UHFFFAOYSA-N 0.000 title claims description 19
• 239000004009 herbicide Substances 0.000 title claims description 17
• 150000001875 compounds Chemical class 0.000 claims description 302
• 125000004432 carbon atom Chemical group C* 0.000 claims description 254
• 239000000203 mixture Substances 0.000 claims description 206
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 185
• -1 cyano, hydroxy Chemical group 0.000 claims description 181
• 229910052799 carbon Inorganic materials 0.000 claims description 151
• 125000000217 alkyl group Chemical group 0.000 claims description 138
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 108
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 99
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 82
• 238000006243 chemical reaction Methods 0.000 claims description 78
• 239000011541 reaction mixture Substances 0.000 claims description 72
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 71
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 71
• 238000010992 reflux Methods 0.000 claims description 67
• 125000003342 alkenyl group Chemical group 0.000 claims description 65
• 125000000304 alkynyl group Chemical group 0.000 claims description 62
• 241000196324 Embryophyta Species 0.000 claims description 57
• 125000003545 alkoxy group Chemical group 0.000 claims description 55
• 238000000034 method Methods 0.000 claims description 48
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 41
• 230000002363 herbicidal effect Effects 0.000 claims description 39
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 38
• 239000003960 organic solvent Substances 0.000 claims description 38
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 37
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 35
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 32
• 239000011734 sodium Substances 0.000 claims description 32
• 229910052708 sodium Inorganic materials 0.000 claims description 32
• 229910052801 chlorine Inorganic materials 0.000 claims description 30
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 27
• 230000012010 growth Effects 0.000 claims description 27
• 238000011282 treatment Methods 0.000 claims description 26
• 239000002253 acid Substances 0.000 claims description 23
• 229910052783 alkali metal Inorganic materials 0.000 claims description 23
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 23
• 239000000460 chlorine Substances 0.000 claims description 23
• 239000002585 base Substances 0.000 claims description 22
• 150000003839 salts Chemical class 0.000 claims description 22
• ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 21
• 229910052700 potassium Inorganic materials 0.000 claims description 21
• 239000011591 potassium Substances 0.000 claims description 21
• 125000003277 amino group Chemical group 0.000 claims description 20
• 230000009467 reduction Effects 0.000 claims description 20
• 150000001340 alkali metals Chemical class 0.000 claims description 18
• 239000003085 diluting agent Substances 0.000 claims description 18
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 18
• 235000021307 Triticum Nutrition 0.000 claims description 17
• 229910052731 fluorine Inorganic materials 0.000 claims description 17
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 15
• 239000011737 fluorine Substances 0.000 claims description 15
• 150000001335 aliphatic alkanes Chemical group 0.000 claims description 14
• 125000005843 halogen group Chemical group 0.000 claims description 14
• 229910052757 nitrogen Inorganic materials 0.000 claims description 14
• 239000002904 solvent Substances 0.000 claims description 14
• OEDUIFSDODUDRK-UHFFFAOYSA-N 5-phenyl-1h-pyrazole Chemical compound N1N=CC=C1C1=CC=CC=C1 OEDUIFSDODUDRK-UHFFFAOYSA-N 0.000 claims description 13
• 239000001257 hydrogen Substances 0.000 claims description 13
• 229910052739 hydrogen Inorganic materials 0.000 claims description 13
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
• 239000004094 surface-active agent Substances 0.000 claims description 13
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 12
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 12
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 12
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 12
• 125000004429 atom Chemical group 0.000 claims description 11
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
• BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 10
• BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 10
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 10
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
• 230000008569 process Effects 0.000 claims description 10
• FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims description 10
• 238000005809 transesterification reaction Methods 0.000 claims description 10
• VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 9
• KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 9
• 230000008030 elimination Effects 0.000 claims description 9
• 238000003379 elimination reaction Methods 0.000 claims description 9
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
• 239000007864 aqueous solution Substances 0.000 claims description 8
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
• IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 8
• 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 8
• 235000004977 Brassica sinapistrum Nutrition 0.000 claims description 7
• 239000003513 alkali Substances 0.000 claims description 7
• 239000003795 chemical substances by application Substances 0.000 claims description 7
• 229910052500 inorganic mineral Inorganic materials 0.000 claims description 7
• 235000010755 mineral Nutrition 0.000 claims description 7
• QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 6
• KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 6
• 239000011149 active material Substances 0.000 claims description 6
• 229910021529 ammonia Inorganic materials 0.000 claims description 6
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 6
• 239000011707 mineral Substances 0.000 claims description 6
• 229910000027 potassium carbonate Inorganic materials 0.000 claims description 6
• 235000011181 potassium carbonates Nutrition 0.000 claims description 6
• 239000012312 sodium hydride Substances 0.000 claims description 6
• 229910000104 sodium hydride Inorganic materials 0.000 claims description 6
• 150000007513 acids Chemical class 0.000 claims description 5
• 125000004450 alkenylene group Chemical group 0.000 claims description 5
• 125000000033 alkoxyamino group Chemical group 0.000 claims description 5
• 125000004694 alkoxyaminocarbonyl group Chemical group 0.000 claims description 5
• 125000002947 alkylene group Chemical group 0.000 claims description 5
• 125000004419 alkynylene group Chemical group 0.000 claims description 5
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
• 230000032050 esterification Effects 0.000 claims description 5
• 238000005886 esterification reaction Methods 0.000 claims description 5
• 125000001424 substituent group Chemical group 0.000 claims description 5
• 240000005979 Hordeum vulgare Species 0.000 claims description 4
• 235000007340 Hordeum vulgare Nutrition 0.000 claims description 4
• 240000007594 Oryza sativa Species 0.000 claims description 4
• 235000007164 Oryza sativa Nutrition 0.000 claims description 4
• WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 4
• 125000004414 alkyl thio group Chemical group 0.000 claims description 4
• NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 claims description 4
• 150000001721 carbon Chemical group 0.000 claims description 4
• 125000001153 fluoro group Chemical group F* 0.000 claims description 4
• 229910052751 metal Inorganic materials 0.000 claims description 4
• 239000002184 metal Substances 0.000 claims description 4
• BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 4
• 235000009566 rice Nutrition 0.000 claims description 4
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
• 238000009333 weeding Methods 0.000 claims description 4
• 244000075850 Avena orientalis Species 0.000 claims description 3
• XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 3
• 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 3
• 229910052794 bromium Inorganic materials 0.000 claims description 3
• 150000003983 crown ethers Chemical class 0.000 claims description 3
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
• 230000000694 effects Effects 0.000 claims description 3
• 125000000623 heterocyclic group Chemical group 0.000 claims description 3
• 238000004519 manufacturing process Methods 0.000 claims description 3
• 239000011736 potassium bicarbonate Substances 0.000 claims description 3
• 229910000028 potassium bicarbonate Inorganic materials 0.000 claims description 3
• 235000015497 potassium bicarbonate Nutrition 0.000 claims description 3
• TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims description 3
• OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 2
• ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 2
• 244000291564 Allium cepa Species 0.000 claims description 2
• 235000002732 Allium cepa var. cepa Nutrition 0.000 claims description 2
• 244000105624 Arachis hypogaea Species 0.000 claims description 2
• 235000007319 Avena orientalis Nutrition 0.000 claims description 2
• 240000002791 Brassica napus Species 0.000 claims description 2
• 240000007124 Brassica oleracea Species 0.000 claims description 2
• 235000003899 Brassica oleracea var acephala Nutrition 0.000 claims description 2
• 235000011301 Brassica oleracea var capitata Nutrition 0.000 claims description 2
• 235000001169 Brassica oleracea var oleracea Nutrition 0.000 claims description 2
• 229920000742 Cotton Polymers 0.000 claims description 2
• 235000002767 Daucus carota Nutrition 0.000 claims description 2
• 244000000626 Daucus carota Species 0.000 claims description 2
• 235000010469 Glycine max Nutrition 0.000 claims description 2
• 244000068988 Glycine max Species 0.000 claims description 2
• 241000219146 Gossypium Species 0.000 claims description 2
• 244000020551 Helianthus annuus Species 0.000 claims description 2
• 235000003222 Helianthus annuus Nutrition 0.000 claims description 2
• 235000004431 Linum usitatissimum Nutrition 0.000 claims description 2
• 240000006240 Linum usitatissimum Species 0.000 claims description 2
• 240000004658 Medicago sativa Species 0.000 claims description 2
• 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 claims description 2
• 235000010627 Phaseolus vulgaris Nutrition 0.000 claims description 2
• 244000046052 Phaseolus vulgaris Species 0.000 claims description 2
• 235000010582 Pisum sativum Nutrition 0.000 claims description 2
• 240000004713 Pisum sativum Species 0.000 claims description 2
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
• 240000008042 Zea mays Species 0.000 claims description 2
• 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 2
• 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 2
• 239000003377 acid catalyst Substances 0.000 claims description 2
• 125000005091 alkenylcarbonylamino group Chemical group 0.000 claims description 2
• 125000003368 amide group Chemical group 0.000 claims description 2
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
• 229910052796 boron Inorganic materials 0.000 claims description 2
• 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
• 235000005822 corn Nutrition 0.000 claims description 2
• 125000005265 dialkylamine group Chemical group 0.000 claims description 2
• 230000004992 fission Effects 0.000 claims description 2
• 235000019253 formic acid Nutrition 0.000 claims description 2
• 125000005842 heteroatom Chemical group 0.000 claims description 2
• 150000002391 heterocyclic compounds Chemical class 0.000 claims description 2
• 150000004678 hydrides Chemical class 0.000 claims description 2
• 150000002466 imines Chemical class 0.000 claims description 2
• 229910052740 iodine Chemical group 0.000 claims description 2
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
• 229910052760 oxygen Inorganic materials 0.000 claims description 2
• 239000001301 oxygen Substances 0.000 claims description 2
• 235000020232 peanut Nutrition 0.000 claims description 2
• 229910052717 sulfur Inorganic materials 0.000 claims description 2
• 239000011593 sulfur Substances 0.000 claims description 2
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 2
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
• ABJSOROVZZKJGI-OCYUSGCXSA-N (1r,2r,4r)-2-(4-bromophenyl)-n-[(4-chlorophenyl)-(2-fluoropyridin-4-yl)methyl]-4-morpholin-4-ylcyclohexane-1-carboxamide Chemical compound C1=NC(F)=CC(C(NC(=O)[C@H]2[C@@H](C[C@@H](CC2)N2CCOCC2)C=2C=CC(Br)=CC=2)C=2C=CC(Cl)=CC=2)=C1 ABJSOROVZZKJGI-OCYUSGCXSA-N 0.000 claims 1
• 235000016068 Berberis vulgaris Nutrition 0.000 claims 1
• 241000335053 Beta vulgaris Species 0.000 claims 1
• 244000098338 Triticum aestivum Species 0.000 claims 1
• 239000003905 agrochemical Substances 0.000 claims 1
• 238000005904 alkaline hydrolysis reaction Methods 0.000 claims 1
• 125000004185 ester group Chemical group 0.000 claims 1
• 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
• 230000008635 plant growth Effects 0.000 claims 1
• 229940124530 sulfonamide Drugs 0.000 claims 1
• WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 196
• 238000002844 melting Methods 0.000 description 145
• 230000008018 melting Effects 0.000 description 145
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 120
• 239000007787 solid Substances 0.000 description 109
• VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 104
• 239000003480 eluent Substances 0.000 description 103
• 238000004587 chromatography analysis Methods 0.000 description 99
• 239000013078 crystal Substances 0.000 description 89
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 78
• 238000002425 crystallisation Methods 0.000 description 73
• 230000008025 crystallization Effects 0.000 description 73
• 239000000243 solution Substances 0.000 description 52
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 45
• 238000002360 preparation method Methods 0.000 description 35
• ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 28
• WBKFWQBXFREOFH-UHFFFAOYSA-N dichloromethane;ethyl acetate Chemical compound ClCCl.CCOC(C)=O WBKFWQBXFREOFH-UHFFFAOYSA-N 0.000 description 26
• 238000003756 stirring Methods 0.000 description 24
• 238000001704 evaporation Methods 0.000 description 23
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
• 239000003208 petroleum Substances 0.000 description 22
• 230000008020 evaporation Effects 0.000 description 21
• HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 20
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 20
• 239000008187 granular material Substances 0.000 description 20
• 239000003921 oil Substances 0.000 description 20
• 235000019198 oils Nutrition 0.000 description 20
• 239000000843 powder Substances 0.000 description 20
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
• 239000004563 wettable powder Substances 0.000 description 18
• JVVRJMXHNUAPHW-UHFFFAOYSA-N 1h-pyrazol-5-amine Chemical compound NC=1C=CNN=1 JVVRJMXHNUAPHW-UHFFFAOYSA-N 0.000 description 17
• 239000012530 fluid Substances 0.000 description 17
• CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 16
• 241000209140 Triticum Species 0.000 description 16
• 239000012141 concentrate Substances 0.000 description 16
• 235000008504 concentrate Nutrition 0.000 description 16
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 16
• ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
• WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
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• HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 14
• 229960000583 acetic acid Drugs 0.000 description 11
• 238000009835 boiling Methods 0.000 description 11
• INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 11
• 239000000725 suspension Substances 0.000 description 11
• YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 11
• ATANUYPSKXKEDC-UHFFFAOYSA-N 3-chlorobutanoyl chloride Chemical compound CC(Cl)CC(Cl)=O ATANUYPSKXKEDC-UHFFFAOYSA-N 0.000 description 10
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 10
• 229960001701 chloroform Drugs 0.000 description 10
• 238000001816 cooling Methods 0.000 description 10
• 238000000227 grinding Methods 0.000 description 10
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• 239000012429 reaction media Substances 0.000 description 9
• 238000005507 spraying Methods 0.000 description 9
• QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 8
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
• 239000004480 active ingredient Substances 0.000 description 8
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 8
• 150000008048 phenylpyrazoles Chemical class 0.000 description 8
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
• PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
• 241000394440 Viola arvensis Species 0.000 description 7
• 238000010438 heat treatment Methods 0.000 description 7
• PVWOIHVRPOBWPI-UHFFFAOYSA-N n-propyl iodide Chemical compound CCCI PVWOIHVRPOBWPI-UHFFFAOYSA-N 0.000 description 7
• 239000002994 raw material Substances 0.000 description 7
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