Thiadiazines, and insecticidal and acaricidal preparations
    22.
    发明授权
    Thiadiazines, and insecticidal and acaricidal preparations 失效
    噻二嗪,杀虫剂和杀螨剂

    公开(公告)号:US5021412A

    公开(公告)日:1991-06-04

    申请号:US328398

    申请日:1989-03-24

    摘要: Novel tetrahydro-1,3,5-thiadiazin-4-ones of the following general formula (I) or their salts which are useful as an insecticidal and acaricidal agent. ##STR1## In the formula, each of R.sup.1 and R.sup.2 represents a halogen atom or a C.sub.1 -C.sub.4 alkyl group; R.sup.3 represents a halogen atom, a C.sub.1 -C.sub.4 alkyl group, a C.sub.3 -C.sub.6 cycloalkyl group, a C.sub.1 -C.sub.4 alkoxy group, an acetyl group, a phenoxy group, a halo-substituted phenoxy group, a benzyl group, a benzyloxy group, a phenylcarbonyl group, a C.sub.1 -C.sub.4 haloalkyloxy group, a C.sub.1 -C.sub.4 haloalkyloxymethyl group, a C.sub.2 -C.sub.4 haloalkenyloxy group, a C.sub.1 -C.sub.4 haloalkylthio group, a C.sub.1 -C.sub.4 haloalkylthiomethyl group, a C.sub.2 -C.sub.4 haloalkenylthio group, a C.sub.1 -C.sub.8 haloalkyl group, a C.sub.2 -C.sub.8 haloalkenyl group, a C.sub.1 -C.sub.8 alkyloxycarbonyl group, a substituted phenoxycarbonyl group, or a substituted pyridyloxy group; m represents 0, 1, 2 or 3; and n represents 0, 1, 2 or 3.These novel thiadiazines are produced by reacting a compound of general formula (II) ##STR2## wherein R.sup.1 and m are as defined above, with a compound of general formula (III) ##STR3## wherein R.sup.2, R.sup.3 and n are as defined above.

    摘要翻译: 具有以下通式(I)的四氢-1,3,5-噻二嗪-4-酮或它们的盐可用作杀虫剂和杀螨剂。 (I)式中,R 1和R 2各自表示卤原子或C 1〜C 4烷基; R3表示卤素原子,C1-C4烷基,C3-C6环烷基,C1-C4烷氧基,乙酰基,苯氧基,卤素取代的苯氧基,苄基,苄氧基, 苯基羰基,C 1 -C 4卤代烷氧基,C 1 -C 4卤代烷氧基甲基,C 2 -C 4卤代烯氧基,C 1 -C 4卤代烷硫基,C 1 -C 4卤代烷硫基甲基,C 2 -C 4卤代链烯基硫基,C 1 -C 8 卤代烷基,C 2 -C 8卤代烯基,C 1 -C 8烷氧基羰基,取代的苯氧基羰基或取代的吡啶氧基; m表示0,1,2或3; 并且n表示0,1,2或3.这些新的噻二嗪通过使通式(II)的化合物(II)(其中R 1和m如上定义)与通式(III)的化合物反应制备, (III)其中R2,R3和n如上所定义。

    Process for producing 3-phenoxybenzyl 2-(4-alkoxyphenyl)-2-methylpropyl
ethers
    23.
    发明授权
    Process for producing 3-phenoxybenzyl 2-(4-alkoxyphenyl)-2-methylpropyl ethers 失效
    2-(4-烷氧基苯基)-2-甲基丙基醚3-苯氧基苄基的制备方法

    公开(公告)号:US4542243A

    公开(公告)日:1985-09-17

    申请号:US540017

    申请日:1983-10-07

    CPC分类号: C07C41/24 C07C41/16 C07C41/30

    摘要: The present invention relates to a process for producing 3-phenoxybenzyl 2-(4-alkoxyphenyl)-2-methylpropyl ethers having excellent insecticidal and acaricidal activities which are represented by formula (IV): ##STR1## wherein R is a lower alkyl group and X.sub.1 and X.sub.2 are each a hydrogen or fluorine atom, which comprises reacting a 3-halogeno-4-alkoxyneophyl halide represented by the formula (I): ##STR2## wherein Y.sub.1 and Y.sub.2 are each a hydrogen, chlorine or bromine atom, at least one of them being a chlorine or bromine atom, R has the same meaning as above and X is a halogen atom, with a 3-phenoxybenzyl alcohol represented by the formula (II): ##STR3## wherein X.sub.1 and X.sub.2 have the same meaning as above, in the presence of a base to obtain a 3-phenoxybenzyl 2-(4-alkoxy-3-halogenophenyl)-2-methylpropyl ether represented by the formula (III): ##STR4## wherein Y.sub.1, Y.sub.2, R, X.sub.1 and X.sub.2 have the same meaning as above, and then subjecting the product to a hydrodehalogenation reaction, and relates to a process for producing a 3-halogeno-4-alkoxyneophyl halide represented by formula (I), which comprises reacting a 2-halogeno-1-alkoxybenzene represented by formula (V): ##STR5## wherein Y.sub.1 and Y.sub.2 are each a hydrogen, chlorine or bromine atom, at least one of them being a chlorine or bromine atom, and R represents a lower alkyl group, with a methallyl halide in the presence of an acid catalyst at -20.degree. to 50.degree. C.

    摘要翻译: 本发明涉及一种具有优异的杀虫和杀螨活性的2-(4-烷氧基苯基)-2-甲基丙醚的3-苯氧基苄基的方法,其由式(Ⅳ)表示:其中R为低级 烷基,X 1和X 2各自为氢或氟原子,其包括使由式(I)表示的3-卤代-4-烷氧基脱乙酰卤:其中Y 1和Y 2各自为氢,氯 或溴原子,其中至少一个为氯或溴原子,R具有与上述相同的含义,X为卤素原子,与式(II)表示的3-苯氧基苄醇: 其中X1和X2具有与上述相同的含义,在碱的存在下得到由式(III)表示的2-(4-烷氧基-3-卤代苯基)-2-甲基丙基3-苯氧基苄基: (III)其中Y1,Y2,R,X1和X2具有与上述相同的含义,然后使产物进行加氢脱卤反应, 涉及制备由式(I)表示的3-卤代-4-烷氧基脱乙酰卤的方法,该方法包括使由式(Ⅴ)表示的2-卤代-1-烷氧基苯:其中Y1和Y2 各自为氢,氯或溴原子,其中至少一个为氯或溴原子,R为低级烷基,在甲酸烯丙酯的卤化物存在下,在-20℃至50℃。

    Method for the preparation of unsaturated dimers of
.alpha.-methylstyrenes
    24.
    发明授权
    Method for the preparation of unsaturated dimers of .alpha.-methylstyrenes 失效
    制备{60-甲基苯乙烯的不饱和二聚体的方法

    公开(公告)号:US3985818A

    公开(公告)日:1976-10-12

    申请号:US520151

    申请日:1974-11-01

    CPC分类号: C07C2/04 C07C2531/10

    摘要: Unsaturated dimers which contain 2,4-diphenyl-4-methyl-1-pentene as their main component (i.e., in an amount of greater than 95%) are produced by reacting an .alpha.-methylstyrene at a temperature of from 20.degree. to 100.degree.C. in the presence of a sulfonic acid type cation-exchange resin catalyst and in the further presence of a primary or secondary monohydric alcohol containing from 2 to 5 carbon atoms. By this reaction, side products including a saturated dimer of 1,1,3-trimethyl-3-phenylindane, trimers and higher polymers are produced only in an extremely small amount. The unsaturated dimers are very useful as a molecular weight modifier when employed, instead of dodecylmercaptans, for the production of polymers such as an ABS resin, an AS resin, and the like.

    摘要翻译: 含有2,4-二苯基-4-甲基-1-戊烯作为其主要成分的不饱和二聚体(即,大于95%的量)通过α-甲基苯乙烯在20℃至100℃的温度下反应 在磺酸型阳离子交换树脂催化剂的存在下进一步存在,并且在另外存在含有2至5个碳原子的伯或仲一元醇的情况下。 通过该反应,仅产生极少量的包含1,1,3-三甲基-3-苯基二氢茚的饱和二聚体,三聚体和更高级聚合物的副产物。 作为分子量调节剂,当使用不饱和二聚体代替十二烷基硫醇,用于生产聚合物如ABS树脂,AS树脂等时是非常有用的。