首页> 外国专利> process for the preparation of new gefos - foryleerde thiofeenverbindingen, methods for the preparation of preparations that contain this. things.and preparations obtained by this method.

process for the preparation of new gefos - foryleerde thiofeenverbindingen, methods for the preparation of preparations that contain this. things.and preparations obtained by this method.

机译:的新gefos的制备方法-来德硫磷酯的制备方法,包括该制剂的制备方法。用这种方法得到的东西和制剂。

摘要

1511413 Phosphorus esters containing a substituted thiophene group ROUSSEL-UCLAF 13 Feb 1976 [14 Feb 1975] 05698/76 Headings C2P and C2C The invention comprises compounds (I) of the formula wherein R 1 is C 1 -C 4 alkyl, R 2 is C 1- C 4 alkyl or -alkoxy, or a radical -NRSP1/SPRSP11/SP wherein RSP1/SP and RSP11/SP are H or C 1 -C 4 alkyl, R 3 is CN, -COOC 1 -C 4 alkyl, or -COZ where Z is C 1 -C 4 alkyl or phenyl, R 4 is C 1 -C 6 alkyl, -alkoxy or -alkythio, phenyl, N-morpholinyl, N-piperidinyl or -COOC 1 -C 4 alkyl, and X is O or S. They may be obtained by reacting in compound (II) with ClP(X)(OR 1 )R 2 preferably in the presence of a basic agent. The compounds (I) have insecticidal, acaricidal and nematocidal properties and may be used as active ingredients in conventional pesticidal compositions. Compounds (II) of the above formula in which R 3 is cyano and R 4 is methoxy, N- morpholino, ethylthio, n-butoxy and n-propyl respectively are stated to be novel and are obtained by reacting a compound (IV) of the formula wherein R 4 SP1/SP corresponds to the specified R 4 group and alk is an alkyl radical with chloroacetonitrile. The compounds (IV) in which R 4 SP1/SP is methoxy and n-butoxy respectively are also stated to be novel and are prepared by reacting 0-methyl- or 0-n-butyl-2-ethoxycarbonyl imidoacetate hydrochloride respectively with H 2 S. Examples are given for the production of the said novel compounds II and IV. The imidoacetate hydrochlorides are also stated to be novel and are prepared in examples by reacting ethyl cyanacetate with methanol or n-butanol respectively in the presence of HCl gas. Ethyl 3-thioxohexanoate is obtained by bubbling H 2 S into ethyl 3-oxo-hexanoate in ethanol saturated with HCl gas at - 10‹ C. and is converted to 2 - cyano - 3 - hydroxy - 5 - propylthiophene by reaction with chloroacetonitrile as above.
机译:包含取代的噻吩基团的1511413磷酸酯ROUSSEL-UCLAF 1976年2月13日[1975年2月14日]标题C2P和C2C本发明包括下式的化合物(I),其中R 1是C 1 -C 4烷基,R 2是C 1-C 4烷基或-烷氧基,或基团-NR 1 R 11 其中R 1 和R 11 为H或C 1 -C 4烷基,R 3为CN,-COOC 1 -C 4烷基或-COZ,其中Z为C 1 -C 4烷基或苯基,R 4为C 1 -C 6烷基, -烷氧基或-烷硫基,苯基,N-吗啉基,N-哌啶基或-COOC 1 -C 4烷基,X为O或S。它们可以通过化合物(II)与ClP(X)(OR 1)反应获得R 2优选在碱性试剂存在下。化合物(Ⅰ)具有杀虫,杀螨和杀线虫性能,可用作常规杀虫组合物中的活性成分。其中R 3为氰基且R 4为甲氧基,N-吗啉代,乙硫基,正丁氧基和正丙基的上式化合物(II)被认为是新颖的,并且是通过使以下化合物(IV)反应而获得的式中R 4 1 对应于指定的R 4基团,并且烷基是带有氯乙腈的烷基。 R 4 1 分别为甲氧基和正丁氧基的化合物(IV)也被认为是新颖的,并且是通过使0-甲基或0-正丁基-2-乙氧基羰基亚氨基乙酸酯反应来制备的盐分别与H 2 S形成盐酸盐。给出了制备所述新型化合物II和IV的实例。所述亚氨基乙酸盐酸盐也被认为是新颖的,并且在实施例中通过使氰乙酸乙酯分别与HCl或甲醇或正丁醇在HCl气体存在下反应制备。 3-硫代己酸乙酯是通过将H 2 S鼓入3-氧代己酸乙酯在10°C的HCl气体中饱和的乙醇中制得的,并通过与氯乙腈反应,转化为2-氰基-3-羟基-5-丙基噻吩。以上。

著录项

  • 公开/公告号NL7601489A

    专利类型

  • 公开/公告日1976-08-17

    原文格式PDF

  • 申请/专利权人 ROUSSEL-UCLAF S.A. TE PARIJS.;

    申请/专利号NL19760001489

  • 发明设计人

    申请日1976-02-13

  • 分类号C07F9/04;A01N9/36;

  • 国家 NL

  • 入库时间 2022-08-23 02:49:17

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