Process for the manufacture of
5-dichloroacetyl-3,3,6-trimethyl-9-oxo-1,5-diazabicyclo�4.3.0! nonane
    3.
    发明授权
    Process for the manufacture of 5-dichloroacetyl-3,3,6-trimethyl-9-oxo-1,5-diazabicyclo�4.3.0! nonane 失效
    制备5-二氯乙酰基-3,3,6-三甲基-9-氧代-1,5-二氮杂双环[4.3.0]壬烷的方法

    公开(公告)号:US5677452A

    公开(公告)日:1997-10-14

    申请号:US736438

    申请日:1996-10-24

    CPC classification number: C07D487/04

    Abstract: The manufacture of 5-dichloroacetyl-3,3,6-trimethyl-9-oxo-1,5-diazabicyclo�4.3.0!-nonane I by the reaction of 3,3,6-trimethyl-9-oxo-1,5-diaza-bicyclo�4.3.0!nonane II with dichloroacetyl chloride in the presence of a solvent and a base, wherein a) this reaction is carried out in a two-phase system comprising a virtually water-insoluble organic solvent and water, and sodium or potassium hydroxide acting as the base is metered in at a rate corresponding to the rate of consumption of the dichloroacetyl chloride such that the aqueous phase exhibits a pH of from 7 to 9, and b) the resulting product is separated.

    Abstract translation: 通过使3,3,6-三甲基-9-氧代-1,2-二氢异喹啉的反应制备5-二氯乙酰基-3,3,6-三甲基-9-氧代-1,5-二氮杂双环[4.3.0] 5-二氮杂 - 双环[4.3.0]壬烷II与二氯乙酰氯在溶剂和碱存在下反应,其中a)该反应在包含实际上不溶于水的有机溶剂和水的两相体系中进行, 以对应于二氯乙酰氯的消耗速率的速率计量作为碱的氢氧化钠或氢氧化钾,使得水相的pH为7-9,并且b)分离得到的产物。

    Preparation of cyclohexane-dione derivatives
    4.
    发明授权
    Preparation of cyclohexane-dione derivatives 失效
    环己酮衍生物的制备

    公开(公告)号:US5118856A

    公开(公告)日:1992-06-02

    申请号:US562445

    申请日:1990-08-02

    Abstract: A process for the preparation of cyclohexanedione derivatives of the general formula I ##STR1## where R.sup.1 is C.sub.2 -C.sub.8 -alkyl, C.sub.2 -C.sub.8 -alkenyl, C.sub.3 -C.sub.12 -cycloalkyl, C.sub.5 -C.sub.12 -cycloalkyl with 0-4 olefinically unsaturated bonds, C.sub.2 -C.sub.8 -alkylthioalkyl, C.sub.6 -C.sub.12 -bicycloalkyl with 0-3 olefinically unsaturated bonds, unsubstituted or substituted aryl or hetaryl, or a heterocyclic radical of 4 to 7 atoms of which not more than 3 may be hetero-atoms chosen from O, S and N, the radical being saturated or olefinically unsaturated, by reacting an .alpha.,.beta.-unsaturated ketone (II) with a dialkyl malonate in the presence of a base to give the alkoxycarbonylcyclohexenolone or its salt (III) ##STR2## and acylation, hydrolysis and decarboxylation of (III), wherein the .alpha.,.beta.-unsaturated ketone (II) is reacted, in the presence of a base, with the dialkyl malonate in a solvent from which the alcohol liberated from the malonate can be distilled off, the alcohol is distilled off, where appropriate as an azeotrope, the salt of the alkoxycarbonylcyclohexenolone is reacted with a carboxylic acid halide and the product, where appropriate after removal of excess acyl halide, is treated with an acylation catalyst, hydrolyzed and decarboxylated.

    Abstract translation: 制备通式I(I)的环己二酮衍生物的方法,其中R 1是C 2 -C 8 - 烷基,C 2 -C 8 - 烯基,C 3 -C 12 - 环烷基,具有0-4烯属的C 5 -C 12 - 环烷基 不饱和键,C 2 -C 8烷硫基烷基,具有0-3烯属不饱和键的C 6 -C 12 - 双环烷基,未取代或取代的芳基或杂芳基,或其中不超过3的4至7个原子的杂环基可以是选择的杂原子 通过在碱存在下使α,β-不饱和酮(II)与丙二酸二烷基酯反应得到烷氧基羰基环己烯醇或其盐,从O,S和N中选择饱和或烯属不饱和基团(III) 和(III)的酰化,水解和脱羧反应,其中α,β-不饱和酮(II)在碱的存在下与丙二酸二烷基酯在可从其中释放出来的丙二酸酯释放的醇的溶剂中反应 关闭,酒精被蒸馏掉,在适当的地方作为azeo 将烷氧基羰基环己烯醇的盐与羧酸卤化物反应,并且在除去过量酰基卤后适当的产物用酰化催化剂处理,水解和脱羧。

    Preparation of aromatic azomethines
    8.
    发明授权
    Preparation of aromatic azomethines 失效
    芳香偶氮甲碱的制备

    公开(公告)号:US4491672A

    公开(公告)日:1985-01-01

    申请号:US155760

    申请日:1980-06-02

    CPC classification number: C07C249/02

    Abstract: Aromatic azomethines are prepared by reacting anilines with formaldehyde and then removing the greater part of the water by distillation, low-boiling alcohols, in certain amounts, being present during the distillation and, if desired, during the reaction or during a part thereof.The aromatic azomethines obtainable by the novel process are valuable starting materials for the preparation of herbicides, especially pre-emergence herbicides and post-emergence herbicides, fungicides, insecticides, bacteriostatic agents, fungistatic agents and vulcanization accelerators.

    Abstract translation: 芳族偶氮甲碱通过苯胺与甲醛反应然后通过蒸馏除去大部分水,一定量的低沸点醇,在蒸馏期间以及如果需要在反应过程中或在其一部分期间进行制备。 通过新方法获得的芳族偶氮甲碱是用于制备除草剂,特别是芽前除草剂和芽后除草剂,杀真菌剂,杀虫剂,抑菌剂,抑菌剂和硫化促进剂的有价值的起始材料。

Patent Agency Ranking