Process for preparing .alpha., .beta.-unsaturated aldehydes
    5.
    发明授权
    Process for preparing .alpha., .beta.-unsaturated aldehydes 失效
    制备α,β-不饱和醛的方法

    公开(公告)号:US4745229A

    公开(公告)日:1988-05-17

    申请号:US15095

    申请日:1987-02-13

    摘要: A process for preparing .alpha.,.beta.-unsaturated aldehydes of the general formula (I) ##STR1## in which R.sup.1, R.sup.2 and R.sup.3 are independently a hydrogen atom, or an alkyl or alkenyl group with or without being substituted with a lower acyloxy group. The aldehyde of the general formula (I) is prepared by reaction between an allylic chloride of the following general formula (IIa) ##STR2## in which R.sup.1, R.sup.2 and R.sup.3 have, respectively, the same meanings as defined above, and an amine oxide selected from the group consisting of tri(lower alkyl)amine N-oxides of the formula,R.sub.3.sup.4 N.sup.+ O.sup.-,in which R.sup.4 represents a lower alkyl group having from 2 to 4 carbon atoms, and N-lower alkylmorpholine N-oxides of the following formula ##STR3## in which R.sup.5 represents a lower alkyl group having from 1 to 4 carbon atoms. Alternatively, the aldehyde of the formula (I) is obtained by reaction between an allylic chloride of the following general formula (IIb) ##STR4## in which R.sup.1, R.sup.2 and R.sup.3 have, respectively, the same meanings as defined above, and an amine oxide selected from the group consisting of tri(lower alkyl)amine N-oxides of the formula,R.sub.3.sup.4 N.sup.+ O.sup.-,in which R.sup.4 has the same meaning as defined above, and N-lower alkylmorpholine N-oxides of the following formula ##STR5## in which R.sup.5 has the same meaning as defined above, in the presence of an alkali metal iodide or a copper halide.

    摘要翻译: 制备通式(I)的α,β-不饱和醛的方法,其中R 1,R 2和R 3独立地为氢原子,或具有或不具有低级烷基或烯基的烷基或烯基 酰氧基。 通式(I)的醛通过以下通式(IIa)的烯丙基氯与其中R 1,R 2和R 3分别具有与上述相同的含义和 选自下列的三(低级烷基)胺N-氧化物的氧化胺,其中R 4表示具有2至4个碳原子的低级烷基的式R 34 N + O-,和N-低级烷基吗啉N- 下式“IMAGE”的氧化物,其中R 5表示具有1至4个碳原子的低级烷基。 或者,式(I)的醛通过以下通式(IIb)的烯丙基氯(IIb)(其中R1,R2和R3分别具有与上述相同的含义) 和选自下式的三(低级烷基)胺N-氧化物的氧化胺,其中R 4具有与上述相同的含义的R 34 N + O-,以及下述的N-低级烷基吗啉N-氧化物 在碱金属碘化物或卤化铜存在下,其中R 5具有与上述相同的含义的式“IMAGE”。

    1,3-Cyclohexanedione derivatives
    7.
    发明授权
    1,3-Cyclohexanedione derivatives 失效
    1,3-环己二酮衍生物

    公开(公告)号:US4336202A

    公开(公告)日:1982-06-22

    申请号:US264463

    申请日:1981-05-18

    摘要: Novel cyclohexanone derivatives of general formula: ##STR1## (wherein R.sup.1 is a hydrocarbon group of 1 to 15 carbon atoms) and new cyclohexanone derivatives of general formula: ##STR2## (wherein R.sup.1 and R.sup.2 each is a hydrocarbon group of 1 to 15 carbon atoms) are produced by an electrooxidative coupling of 1,3-cyclohexanedione with a vinyl ether of general formula:CH.sub.2 .dbd.CH-O-R.sup.1(wherein R.sup.1 is as defined above) in the presence or absence of an alcohol of general formula:R.sup.2 OH(wherein R.sup.2 is as defined above). These new cyclohexanone derivatives can be easily converted to N-substituted or unsubstituted-4-oxo-4,5,6,7-tetrahydroindoles, which are of value as intermediates for the production of N-substituted or unsubstituted-4-hydroxyindoles and, thence, to pindolol and its analogs.

    摘要翻译: 新型的通式为:IMA(其中R 1为1至15个碳原子的烃基)的环己酮衍生物和通式为新的环己酮衍生物:其中R1和R2各自为1至15个碳原子的烃基 原子)通过在通式R 2 OH的存在或不存在的情况下,通过1,3-环己二酮与通式为CH 2 = CH-O-R 1(其中R 1如上定义)的乙烯基醚的电氧偶合而产生 (其中R2如上所定义)。 这些新的环己酮衍生物可以容易地转化成N-取代或未取代的-4-氧代-4,5,6,7-四氢吲哚,它们作为制备N-取代或未取代的4-羟基吲哚的中间体, 因此,对吲哚洛尔及其类似物。