• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    1423376 Diphenylether derivatives ROHM & HAAS CO 13 March 1973 [14 March 1972 (2) 12 Feb 1973 (2)] 11954/73 Heading C2C The invention comprises compounds of the formula where X is hydrogen, halogen, trihalomethyl, C 1 -C 4 alkyl or cyano and (i) Y is halogen, trihalomethyl or, except where X is chlorine, hydrogen and Z is hydrogen or (ii) Y is hydrogen, halogen or trihalomethyl and Z is alkoxy, alkoxyalkoxy, hydroxyalkoxy, carboxyalkoxy, carbalkoxyalkoxy, halogen, alkylthio, alkyl, amino substituted with a dialkylcarbamoyl group, one or two alkyl groups, an alkylcarbonyl group or a carbalkoxy group, carboxy, carbalkoxy, carboxyalkyl or carbalkoxyalkyl. The compounds may be prepared by reacting a suitably substituted phenol or the potassium or sodium salt thereof with a halobenzene compound, or by introducing a substituent into a diphenyl ether. The compounds may be used as herbicides.
    公开号:SU713520A3
    申请号:SU731898369
    申请日:1973-03-13
    公开日:1980-01-30
    发明作者:Отто Байер Хорст；Свитенбанк Колин；Янгминг.И Рой
    申请人:Ром Энд Хаас Компани (Фирма)；
    IPC主号:
    专利说明:

    (.54) HERBICIDE COMPOSITION
    The present invention will be applied to chemical agents to combat undesirable agent, which is associated with three plants.
    Known heroul day composition based on derivatives D1i | The enlarged v (|) iipoB (|) 3.5 XiCeH-.O Sbn.;. From. | de X-C, Me. .Og group. n 2 or 4 2, 4, as well as such as 3-tr,; Hormetn.t-4-nitrodpheny.
    The terbnnidic composition is known on the basis of and | waterstars ;; itrod} fennloto ether of the formula
    SRt
    ABOUT
    about
    ten
    6
    -Halper; a. - water gulp: h; :: R - metoke} t L n.iJi saturated n1 erd 1. However, the well-known herbicidal compositions have not been distributed; from pol1; from 1n the balance of broadleaf ::: stentiums and odnogolnykh in cereal govos; x. In order to enhance the herbicidal activity and the austerity of the action of the predisposition, a.ioreii. Trift Ormetnl, K1) L with chg1slom ATOMOv corner) to 4:; li c K1: Ogre Nla; ;: L; ged}: L1 tr1i |) tormaU5odorod. o; c; g: up11a. alko.sngrunsha to () childbirth. alknlpa. having up to 4 ltyols, uroi a .ioreif ;;. alinoggdta. Alkyltno: Alyuyuschaya to 4 carbon atoms, pn. carboxyl} 1 G1tuina, carl soil ..; -1m oydp to 4 ator in alkox; 1, fornon parts, ka; 1plna rDvnns. - meyunha up to 4 carbon atoms, carbalkoxy. per group having up to 6 carbon atoms, alkanoyloxy group having up to 4 carbon atoms, or carbamoyloxy group having up to 6 carbon atoms. as well as an additive selected from the group of solvent, emulsifier, dispersing agent (and, moreover, the weight of active ingredient ranges from 2 to 98% by weight). % Gerbptspdia kompotsptsp and its analysis are given in table. i; in tab. 2 shows the indicator of the gericidal activity of the proposed COMNOSITS1. t p about l and c and I
    Tocr- i; i4ii; e
    74 81 92 85
    and I M-lCHaCFijOH
    WITH
    II AXLE.SOOLS Cl
    I
    and OCM, CO, C, H; Cl
    MLI OSH (VIS) Cl Cl C
    II
    PI OCH (SNZ) CO, C, H5
    and I NH.
    and
    Cl
    OSISNIOS SI
    n and l-I I-II
    Cl och (SNZ) C SP Cl OOSACHaOSCH Cl Cl Cl Cl
    axis (SNS) jays,
    CCA T1S1-
    M-ICOC.HS
    HUSCO C1 Cl
    SNS Cl
    C1 Cl
    about
    /
    shifts
    Cl Cl
    OCHoCHOHClljOti
    11 II I and and OCI-bCl-l.SCIb Cl Cl
    (SzN7-p) 2
    OCFL.CH.SOjCH. Cl
    (CH3) CH, CHOHOH Cl Cl Cl Cl
    NHCOKHCIb
    P
    N4-ICOSC, M, i
    II m
    N (COSC, H5) i
    with to
    with I
    A
    Cl
    SAL1 Cl Cl
    Sozsmz
    II and 11 11 n n
    axis (CH3) with, CH3 Cl Cl; SNS (SNS)
    COH (CH3) SOHMSN, Cl Cl
    OCH (,) CO (CfI ::,) I (CaH5) CH2CH, Cl Cl
    N (C, Il5) CO.HCH3
    46.22 47.82 45.96 46.00 48.49 .60 4 7, 34, 34.35 49.78 49.8, 48.60 46.98
    180-185
    (0.04
    M RT. Art.) I {4 - ia55
    14.33 14.80 15.27 14.80 14.49 14, .12 14.26 14.12 14.76 14.00 14.71 14.08 14.90 13.93 16.95 17.19 18 48 48, 9
    Continued table. 2
    S, i
    7-s
    ABOUT
    four
    5D
    note:
    权利要求:
    Claims (3)
    [1]
    Invention Formula
    A herbicidal composition comprising an active principle based on 4-trifluoromethyl-4-nitro-prophenyl ether DERIVATIVES, as well as an additive selected from the group of a solvent, an emulsifier, a dispersant, about 1 hr; :. K) 1ts and with R telts, that. in order to enhance the 1-obicide of OI activity and selective; it contains 4-trifluoromethyl-4-n as it is irpidic 4-trifluoromethyl-4, itrodiphepyloxy ether; is a compound of the general form II where X is halogen, tr1 (|) tormetp, t} extrinsic alkyl with 15 carbon atoms from I to 4 or u; 1 ny 1pp; Y -) d. halogen) or 1tr; krto; 1metid; Z is hydrogen, oKCHrpyniia, alkoxprui-20 ia, and ieyui to ij atoms of carbon alkyl; ) aruyaa, imkm.cha up to 4 atoms .ia,;: halogen volume, a.migruguiaia, alky,: gigogroup. :: a. have .y 4 atoms of lchlerod, usiaHO | -ruiiia, carboxyl primer, carbalkok-25 si. gruii, having up to 4 atoms of yi.irode in the alkoxyl idio part, carboxyalkyl: that grunia, a termea to 4 carbon atoms, a carbalkoxyalkyl group, having up to () atoms of y-lyud, alkaioyloxngrun, 30 nomerio1 to 4 carbon atoms, go KajKiamonloxygrunna, | I., which has up to G carbon atoms, and the amount of weight content contained in the act;) Often, it ranges from 2 to 98 weight. / h 5 10 Priority on the basis of signs: 14.03.72 with Z - Bo; io | joa, a.iKOKciirpyiina, had () an atom of hlsrol. alkyl group :: a, having: t 4 atoms of carbon, atom 1al () 1mm1a, II alk1 ltiogr-ppa, having 4 .iTo.Moii yr.iejTOia. 12.02. 73 with X - ;; o; the fool, halogen, trifluorme:; 1Л. Hii.-iujnn alkyl by the number of carbon atoms,; and from 1 to -} or shagaiogroup; g; odo, chod, i i; ioixn и, 1и т) и (j) - - oxygrunia, а.миогиииа. cyano. | -ru11ia, carboxylia of the soil, carbalkoS11lüruiii, and it has up to 4 carbon atoms. Croda in the alcohol part, carboxa, IpyHiia lcilla, imemia and up to 4 carbon atoms. carbadkoxyadule group: 1ms (). about carbon atoms, alkanoylOKciirpyinia, .mile1O1a.cho 4 carbon atoms i.-ni carba (5) 1, k) 1 ui P1P1a, having: w b atolls at merod, Petochikiki kn (po }) The proceedings accepted by the z: nimaii irie examination: I. France Patent As 20651G3, cl. A 01 X (), C 07 C 79/00, oublenk. 1970.
    [2]
    2. Pate} Mr. Yaionnn L 13038, cl. 30 F 371, Mr. Pub. 1971
    [3]
    3. Patent Ang.cn L1 1014802, cd. L 5 EL 01 X 9/12,. 1963. 4. 11ATilJ.-l L 3454392, cl. 71-124. , 909.
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    同族专利:
    公开号 | 公开日
    GB1423376A|1976-02-04|
    OA04348A|1980-01-31|
    JPS49236A|1974-01-05|
    AU5328973A|1974-09-19|
    FR2175997B1|1977-02-04|
    KE2734A|1977-05-27|
    AR208495A1|1977-02-15|
    NL174825B|1984-03-16|
    DK144561B|1982-03-29|
    CH567359A5|1975-10-15|
    PH18682A|1985-08-29|
    RO77037A|1981-08-30|
    HU172709B|1978-11-28|
    IL41766D0|1973-05-31|
    TR18291A|1976-12-28|
    JPS5825641B2|1983-05-28|
    DK144561C|1982-09-20|
    SE416544B|1981-01-19|
    FR2175997A1|1973-10-26|
    IL41766A|1977-04-29|
    IE37575B1|1977-08-31|
    IT983545B|1974-11-11|
    IN138701B|1976-03-20|
    IE37575L|1973-09-14|
    AU467605B2|1975-12-04|
    LU67204A1|1973-09-14|
    NL7303590A|1973-09-18|
    NL174825C|1984-08-16|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    FR1602719A|1968-11-22|1971-01-18|Herbicidal diphenylether/pheny urea compos - ition |USRE32243E|1969-04-25|1986-09-09|Rhone-Poulenc Agrochimie|Esters of substituted phenoxybenzoic acids, compositions of the same and herbicidal use thereof|
    USRE32216E|1969-04-25|1986-07-29|Rhone-Poulenc Agrochimie|Salts of substituted phenoxybenzoic acids, compositions of the same and herbicidal use thereof|
    USRE32215E|1971-02-11|1986-07-22|Rhone-Poulenc Agrochimie|Substituted phenoxybenzoic acids compositions of the same and herbicidal use thereof|
    JPS5436209B2|1972-10-24|1979-11-08|
    EG11593A|1973-07-03|1980-07-31|Bayer Ag|Halogenated 4-trifluiromethyl-4-cyano-diphenyl-ethers process for their preparation and their use as herbicides|
    JPS5068800U|1973-10-22|1975-06-19|
    JPS5724761B2|1973-12-19|1982-05-26|
    JPS50123824A|1974-03-15|1975-09-29|
    JPS50132125A|1974-04-12|1975-10-20|
    JPS5726561B2|1974-12-23|1982-06-05|
    JPS5726642B2|1977-06-15|1982-06-05|
    DE2938595A1|1979-09-24|1981-04-23|Celamerck Gmbh & Co Kg, 6507 Ingelheim|METHOD FOR PRODUCING DIPHENYL ETHERS|
    DE2942930A1|1979-10-24|1981-05-27|Basf Ag, 6700 Ludwigshafen|SUBSTITUTED UREAS, THEIR PRODUCTION AND USE AS HERBICIDES|
    DE3045805A1|1980-12-05|1982-07-08|Basf Ag, 6700 Ludwigshafen|DIPHENYL ETHER, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS HERBICIDES|
    DE3269621D1|1981-08-07|1986-04-10|Ciba Geigy Ag|Phenoxyphenyl-aminocarboxylic-acid derivatives, their preparation, compositions containing them and their use|
    JP2801181B2|1983-01-10|1998-09-21|キヤノン株式会社|Sheet reversing device|
    FR2549047B1|1983-07-12|1986-03-21|Rhone Poulenc Agrochimie|NOVEL HERBICIDES DERIVED FROM ARYLOXYBENZENES CARBONIMIDES|
    EP0161529B1|1984-05-18|1989-07-12|Asahi Kasei Kogyo Kabushiki Kaisha|2-nitro-5-phenylacetic ester, thioester and amide, process for preparation therof, herbicidal composition, and method for destruction of undesirable weeds|
    HU193466B|1984-11-12|1987-10-28|Budapesti Vegyimuevek|Fungicidal composition comprising 2-nitrobenzoic acid derivative as active substance|
    JPS63157065U|1987-04-02|1988-10-14|
    DE69902987T2|1998-12-23|2003-01-23|Dow Agrosciences Llc|Manufacture of diphenyl ethers|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US23465172A| true| 1972-03-14|1972-03-14|
    US234656A|US3888932A|1972-03-14|1972-03-14|Herbicidal 4-trifluoromethyl-4-nitrodiphenyl ethers|
    US05331719|US3928416A|1972-03-14|1973-02-12|Herbicidal 4-trifluoromethyl-4{40 nitrodiphenyl ethers|
    US05/331,947|US4076741A|1972-03-14|1973-02-12|Herbicidal 4-trifluoromethyl-4-nitrodiphenyl ethers|
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