首页> 外国专利> COMPOUNDS CONTAINING AN UNSATURATED ALIPHATIC CHAIN HAVING AN INSECTICIDAL ACTION AND HAVING AN INHIBITING EFFECT ON THE DEVELOPMENT AND METAMORPHOSIS OF INSECTS

COMPOUNDS CONTAINING AN UNSATURATED ALIPHATIC CHAIN HAVING AN INSECTICIDAL ACTION AND HAVING AN INHIBITING EFFECT ON THE DEVELOPMENT AND METAMORPHOSIS OF INSECTS

机译:包含不饱和脂肪链的化合物具有杀虫作用并具有抑制作用,可促进昆虫的发生和经复分解

摘要

1497570 Chlorovinylated compounds and their preparation MONTEDISON SpA 13 Jan 1975 [11 Jan 1974 18 Oct 1974] 1366/75 Heading C2C Compounds having the general formula in which: X represents a hydrogen or chlorine atom, n and t are each 1 or 2, m, p, q, r and s are each 0, 1 or 2, each R represents a hydrogen atom or a C 1-3 alkyl group which may be branched and/or substituted with the proviso that in the group -(CR = CR) n - at least one of the groups R represents -CH 3 or -C 2 H 5 , A and B each represents a hydrogen atom, or A and B together represents and extra bond so forming a double bond between the two carbon atoms to which they are attached, Z represents ORSP1/SP, or -SRSP1/SP, -SCSORSP1/SP, -CN, -NRSP11/SPRSP111/SP or -COY RSP1/SP represents a C 1-3 alkyl group a C 2-4 alkenyl group, an oxalkyl group, or C 6 H (5-Á) W Á , Á is 0, 1, 2 or 3, W represents a hydrogen or halogen atom, a C 1-5 alkyl group a C 2-4 alkenyl group, an alkoxy group, an alkylthio group, an alkoxy carboxyl group, a keto group, an alkyl carboxyl, -NO 2 , -CN, a phenyl group, a methylanedioxy group linked for example at the 3, 4 positions to the C 6 H (5-Á) nucleus, or an amino group optionally substituted with one or more monovalent substituents or with a substitutuent which together with the nitrogen atom completes a heterocyclic ring, RSP11/SP and RSP111/SP, which may be the same as or different from one another, each represents a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms or an alkenyl group containing 2 to 4 carbon atoms or the group; or RSP11/SP and RSP111/SP, together with the nitrogen atom form a 5, 6 or 7-membered heterocyclic ring, Y represents a hydrogen atom, or an alkyl group containing 1 to 5 carbon atoms, an alkoxy group containing 1 to 5 carbon atoms, -OH, -O-metal, a cycloalkyl group or an aryl group, and M represents -CH 2 - or -CO-. The compound may be prepared in a series of reactions in which (a) carbon tetrachloride is reacted with a diene of formula to give a chloro-derivative of the formula CCl 3 -CH 2 -CR=CH-CH 3 Cl, (b) the latter is reacted with a keto-acid of the formula in which RSP1/SP has the same meanings as R, to obtain a compound of the formula (c) the product of step (b) is decarboxylated to give the compound (d) HCl is removed from the product of step (c) to give the ketone of formula or the compound obtained in step (c) is hydrogenated to give the saturated compound which is subsequently converted, by removal of HCl, to an unsaturated ketone of the formula (e) the unsaturated ketone obtained in step (d), generically denoted A-COR wherein A is the radical CCl 2 = CH-CR = CH-CH 2 -CHRSP1/SP- or the radical CCl 2 = CH-CHR-(CH 2 ) 2 -CHRSP1/SP-, is reacted either with a vinyl magnesium bromide of formula R-CH=CR-Mg-Br, or with a vinyllithium salt of formula in order to give the unsaturated alcohol of the general formula (f) the alcohol from step (e) is dehydrated and halogenated to give the compound in which XSP1/SP represents a halogen atom, and (g) the product from step (f) is reacted with a compound of formula ZH. The carbon chain of the product thus obtained may be lengthened further by reacting the halogen derivative obtained in step (f) with a keto-acid of the formula R-CO-CHRSP1/SP-COOC 2 H 5 in a manner similar to that employed in step (b), to give a keto-ester of the formula which may then be reacted further as in steps (c), (d), (e) and (f) above. Products in which Z represents -COY may be obtained by reacting the ketone of the formula A-COR according to a Wittig reaction with a phosphine of the general formula or with a phosphonate of the formula or according to another Wittig synthesis. The products possess insecticidal properties.
机译:1497570氯丁酰化的化合物及其制备MONTEDISON SpA 1975年1月13日[1974年1月11日1974年10月18日] 1366/75标题C2C具有以下通式的化合物:X代表氢或氯原子,n和t分别为1或2,m ,p,q,r和s分别为0、1或2,每个R代表氢原子或C 1-3烷基,可以分支和/或取代,但条件是-(CR = CR )n-基团R中的至少一个代表-CH 3或-C 2 H 5,A和B各自代表一个氢原子,或者A和B一起代表一个或多个额外的键,因此在两个碳原子之间形成一个双键Z代表OR 1 或-SR 1 ,-SCSOR 1 ,-CN,-NR 11 < / SP> R 111 或-COY R 1 表示C 1-3烷基,C 2-4烯基,氧代烷基或C 6 H(5 -Á)WÁ,A为0、1、2或3,W代表氢或卤素原子,C 1-5烷基,C 2-4烯基,烷氧基,烷基硫基,烷氧基羧基,酮基,烷基羧基,-NO 2,-CN,苯基,甲撑二氧基,例如在C 6 H(5-Á)核的3、4位连接,或任选被一个或多个一价取代基或取代基取代的氨基,该取代基与氮原子一起完成杂环R 11 和R 111 彼此相同或不同,分别表示氢原子或碳数1〜4的烷基或碳原子数2〜4的烯基或该基团。或R 11 和R 111 与氮原子一起形成5元,6元或7元杂环,Y代表氢原子或含1的烷基碳原子数为5〜5的碳原子数为1〜5的烷氧基,-OH,-O-金属,环烷基或芳基,M为-CH 2-或-CO-。该化合物可以在一系列反应中制备,其中(a)使四氯化碳与下式的二烯反应以得到下式的氯代衍生物:CCl 3 -CH 2 -CR = CH-CH 3 Cl,(b)后者与下式的酮酸反应,其中R 1 与R具有相同的含义,以获得式(c)的化合物,将步骤(b)的产物脱羧为得到化合物(d)。从步骤(c)的产物中除去HCl,得到下式的酮或将步骤(c)中获得的化合物氢化,得到饱和的化合物,随后将其通过除去HCl而转化为式(e)的不饱和酮,是在步骤(d)中获得的不饱和酮,一般表示为A-COR,其中A是基团CCl 2 = CH-CR = CH-CH 2 -CHR 1 -或基团CCl 2 = CH-CHR-(CH 2)2 -CHR 1 -与式R-CH = CR-Mg-Br的乙烯基溴化镁反应或与式的乙烯基锂盐,以产生不饱和键通式(f)的醇,将步骤(e)的醇脱水并卤化,得到其中X 1 代表卤原子的化合物,以及(g)步骤(f)的产物)与式ZH化合物反应。通过将步骤(f)中获得的卤素衍生物与式R-CO-CHR 1 -COOC 2 H 5的酮酸在室温下反应,可以进一步延长由此获得的产物的碳链。以类似于步骤(b)中所采用的方式,得到下式的酮基酯,然后可以使其与上述步骤(c),(d),(e)和(f)进一步反应。 Z代表-COY的产物可通过根据Wittig反应使通式A-COR的酮与通式的膦或与通式的膦酸酯或根据另一Wittig的合成反应而获得。该产品具有杀虫性能。

著录项

  • 公开/公告号GB1497570A

    专利类型

  • 公开/公告日1978-01-12

    原文格式PDF

  • 申请/专利权人 MONTEDISON SPA;

    申请/专利号GB19750001366

  • 发明设计人

    申请日1975-01-13

  • 分类号C07C121/50;A01N9/00;C07C43/14;C07C49/20;C07C57/02;C07C69/52;C07C87/26;C07C121/30;C07C147/14;C07C149/14;C07C149/34;C07C154/02;C07D317/64;

  • 国家 GB

  • 入库时间 2022-08-22 21:40:13

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