Herbicidal 4-alkoxy- and 4-(substituted)amino-arylpyrrolinone derivatives
    33.
    发明授权
    Herbicidal 4-alkoxy- and 4-(substituted)amino-arylpyrrolinone derivatives 失效
    除草剂4-烷氧基 - 和4-(取代的)氨基 - 吡咯烷酮衍生物

    公开(公告)号:US5191089A

    公开(公告)日:1993-03-02

    申请号:US565536

    申请日:1990-08-09

    CPC分类号: A01N43/36 C07D207/38

    摘要: Herbicidal 4-alkoxy- and 4-(substituted)amino-arylpyrrolinone derivatives of the formula ##STR1## in which X and Y independently of one another represent hydrogen, halogen, alkyl, alkoxy, halogenoalkyl or in each case unsubstituted or substituted aryloxy or arylthio,Z represents halogen, alkyl or alkoxy,n represents the number 0, 1, 2 or 3,A represents in each case unsubstituted or in each case halogen-substituted alkyl, alkenyl, alkynyl, alkoxyalkyl, polyalkoxyalkyl or alkylthioalkyl, cycloalkyl which is optionally interrupted by hetero atoms, arylalkyl which is unsubstituted or substituted by halogen, alkyl, halogenoalkyl, alkoxy and/or nitro, unsubstituted aryl or aryl substituted by a member selected from the group consisting of halogen, alkyl, alkoxy, halogenoalkyl, halogenoalkoxy and phenoxy or phenylthio which are in each case unsubstituted or substituted by halogen, alkyl, alkoxy, halogenoalkyl and/or halogenoalkoxy,B represents hydroxyl, alkoxy, halogenoalkoxy or cycloalkoxy, the cycloalkyl radical being unsubstituted or substituted by halogen and/or alkyl, orB represents the group ##STR2## wherein C and D independently of one another represent hydrogen, alkyl, alkenyl, alkoxyalkyl, alkylthioalkyl or polyalkoxyalkyl, cycloalkyl which is optionally interrupted by hetero atoms or in each case unsubstituted or substituted phenyl, phenylalkyl, phenoxyalkyl, hetaryl or hetarylalkyl, orC and D together with the nitrogen atom to which they are bonded, form a 3- to 9-membered, optionally substituted ring which is optionally interrupted by the further hetero atoms,with the proviso that at least one radical X, Y or Z does not represent chlorine or methyl if B represents hydroxyl and A has a meaning other than optionally substituted aryl.

    摘要翻译: 式(I)的除草4-烷氧基 - 和4-(取代的)氨基 - 芳基吡咯烷酮衍生物,其中X和Y彼此独立地代表氢,卤素,烷基,烷氧基,卤代烷基或在各种情况下是未取代或取代的 芳氧基或芳硫基,Z表示卤素,烷基或烷氧基,n表示数0,1,2或3,A表示各自为未取代的或在各种情况下为卤素取代的烷基,烯基,炔基,烷氧基烷基,聚烷氧基烷基或烷硫基烷基,环烷基 烷基,卤代烷基,烷氧基和/或硝基,未经取代的芳基或被选自卤素,烷基,烷氧基,卤代烷基,卤代烷氧基的成员所取代的芳基, 苯氧基或苯硫基,其各自为未被取代或被卤素,烷基,烷氧基,卤代烷基和/或卤代烷氧基取代,B代表羟基,烷氧基,卤代烷氧基或环 烷氧基,环烷基是未取代的或被卤素和/或烷基取代,或B表示基团,其中C和D彼此独立地表示氢,烷基,烯基,烷氧基烷基,烷硫基烷基或聚烷氧基烷基,任选地中断的环烷基 通过杂原子或在每种情况下未取代或取代的苯基,苯基烷基,苯氧基烷基,杂芳基或杂芳基烷基,或C和D与它们所键合的氮原子一起形成3至9元任选取代的环,其任选地 被另外的杂原子中断,条件是至少一个基团X,Y或Z不表示氯或甲基,如果B表示羟基,并且A具有除任选取代的芳基以外的含义。

    Herbicidal cycloalkyl-substituted thiadiazolyloxyacetamides
    34.
    发明授权
    Herbicidal cycloalkyl-substituted thiadiazolyloxyacetamides 失效
    除草剂环己基取代的三羟甲基纤维素

    公开(公告)号:US5169427A

    公开(公告)日:1992-12-08

    申请号:US706127

    申请日:1991-05-28

    CPC分类号: C07D285/13 A01N43/82

    摘要: Herbicidal cycloalkyl-substituted thiadiazolyloxyacetamides of the formula ##STR1## in which R.sup.1 represents hydrogen, or represents an optionally substituted radical selected from the group consisting of alkyl, alkenyl, alkynyl and aralkyl,R.sup.2 represents an optionally substituted radical selected from the group consisting of alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aralkyl, aryl, alkoxy, alkenyloxy and alkynyloxy, orR.sup.1 and R.sup.2, together with the nitrogen atom to which they are bonded, form an optionally substituted saturated or unsaturated nitrogen-heterocyclic radical, which can contain further hetero atoms and to which a benzo grouping can be fused, andR.sup.3 represents optionally substituted cycloalkyl.Intermediates of the formula ##STR2## are also new.

    摘要翻译: 式(I)的除草环烷基取代的噻二唑氧基乙酰胺,其中R 1表示氢,或表示任选取代的选自烷基,烯基,炔基和芳烷基的基团,R 2表示任选取代的基团,其选自 由烷基,烯基,炔基,环烷基,环烯基,芳烷基,芳基,烷氧基,烯氧基和炔氧基组成,或者R1和R2与它们所键合的氮原子一起形成任选取代的饱和或不饱和的氮杂环基, 其可以含有另外的杂原子,并且苯并基团可以被稠合,并且R 3表示任选取代的环烷基。 公式的中间体也是新的。

    Process for the preparation of halogenomethylketones, in particular of
1,1,1-trifluoroacetone
    35.
    发明授权
    Process for the preparation of halogenomethylketones, in particular of 1,1,1-trifluoroacetone 失效
    制备卤代甲基酮的方法,特别是1,1,1-三氟乙酸

    公开(公告)号:US5093532A

    公开(公告)日:1992-03-03

    申请号:US739112

    申请日:1991-07-31

    摘要: Halogenomethylketones are prepared from nitro compounds by treating the latter in alcoholic solution with sodium alkoxide or potassium alkoxide, cooling to a temperature in the range -10.degree. to -100.degree. C. and then allowing the mixture to react with ozone at -10.degree. to -100.degree. C. The process is particularly suitable for the preparation of 1,1,1-trifluoroacetone from 1,1,1-trifluoro-2-nitropropane.

    摘要翻译: 卤化甲基酮由硝基化合物制备,通过在醇溶液中用醇钠或醇钾处理后者,冷却至-10〜-100℃的温度,然后使混合物与-10℃〜 -100℃。该方法特别适用于从1,1,1-三氟-2-硝基丙烷制备1,1,1-三氟丙酮。

    Process for the preparation of nitromethylene derivatives
    37.
    发明授权
    Process for the preparation of nitromethylene derivatives 失效
    硝基亚甲基衍生物的制备方法

    公开(公告)号:US4767864A

    公开(公告)日:1988-08-30

    申请号:US2837

    申请日:1987-01-13

    IPC分类号: C07D401/06 C07D401/08

    CPC分类号: C07D401/06

    摘要: A process for the preparation of a nitromethylene derivative of the formula (I) ##STR1## in which R represents hydrogen or lower alkyl,m represents the numbers 2, 3 or 4, andn represents the numbers 0, 1, 2 or 3, comprising reacting a diamine of the formula (II), ##STR2## in which R, m and n have the abovementioned meanings, with a fluoronitroethane derivative of the formula (IV)CFX.sup.1 X.sup.2 --CH.sub.2 --NO.sub.2 (IV)in whichX.sup.1 and X.sup.2, independently of one another, represent fluorine or chlorine,in the presence of a base and if appropriate in the presence of a diluent, at temperatures between -10.degree. C. and +100.degree. C. The nitromethylene derivatives have insecticidal properties.

    摘要翻译: 制备式(I)的硝基亚甲基衍生物的方法其中R表示氢或低级烷基,m表示2,3或4号,n表示数字0,1,2 或者3,包括使式(II)的二胺,其中R,m和n具有上述含义的式(II)的二氯化物与式(Ⅳ)CFX1X2-CH2-NO2(Ⅳ)的氟硝基乙烷衍生物反应, 其中X1和X2彼此独立地表示氟或氯,在碱的存在下,如果合适的话,在稀释剂存在下,在-10℃至+ 100℃之间的温度下。硝基亚甲基衍生物具有 杀虫性。