Process for the manufacture of acetoacetyl-aminobenzenes
    2.
    发明授权
    Process for the manufacture of acetoacetyl-aminobenzenes 失效
    乙酰氨基 - 氨基苯甲酸的制备方法

    公开(公告)号:US4169851A

    公开(公告)日:1979-10-02

    申请号:US957041

    申请日:1978-11-02

    CPC分类号: C07C231/04

    摘要: The N-acetoacetylamino compounds of 2,5-dimethoxy-4-chloro-aniline, 2,4-dimethyl-aniline and 2-methyl-5-chloroaniline are obtained in a good yield and excellent purity, if the above-mentioned anilines are reacted with diketene in an inert organic solvent or diluent in the presence of from 0.1 to 6%, calculated on the weight of the aniline, of water, while adding catalytic amounts of acid. An industrial aniline quality is preferably dried by heating it with a solvent forming with water an azeotropic mixture, and thereafter the amount of water required is added. The products may be used without purification as coupling components for the preparation of pigments.

    Process for the preparation of aromatic amines
    3.
    发明授权
    Process for the preparation of aromatic amines 失效
    芳香胺的制备方法

    公开(公告)号:US4375561A

    公开(公告)日:1983-03-01

    申请号:US318117

    申请日:1981-11-04

    CPC分类号: C07C209/68

    摘要: Aromatic amines are obtained from the corresponding cycloaliphatic oximes by heating the oxime to a temperature of from 150.degree. to 350.degree. C. in an ether group containing solvent in the presence of a catalyst containing a noble metal of the 8th auxiliary group of the Periodic Table of Elements. The solvent is preferably an aliphatic ether, especially a lower dialkyl ether of a polyethyleneglycol.

    摘要翻译: 在含有第8族元素周期表的贵金属的催化剂存在下,通过将肟在含有醚基的溶剂中加热至150℃至350℃的温度,从相应的脂环族肟得到芳族胺 的元素。 溶剂优选为脂族醚,特别是聚乙二醇的低级二烷基醚。

    Cyclohexanones and cyclohexenones
    5.
    发明授权
    Cyclohexanones and cyclohexenones 失效
    环己酮和环己烯酮

    公开(公告)号:US4332941A

    公开(公告)日:1982-06-01

    申请号:US195840

    申请日:1980-10-10

    CPC分类号: C07D295/088 C07C45/673

    摘要: Cyclohexanones and -hexenones ##STR1## R.sup.1 is hydrogen or--CO--O--C.sub.n H.sub.2n+1-m (--NR.sup.4 R.sup.5) (1c)R.sup.2 is a group 1c, R.sup.3 is C.sub.1 - to C.sub.10 -alkyl, phenyl or phenyl substituted by lower alkyl, lower alkoxy, trifluoromethyl, nitro, cyano, chloro, carbamoyl, lower-alkyl-carbamoyl, sulfamoyl or lower-alkyl-sulfamoyl, R.sup.4 and R.sup.5 are lower alkyl or --NR.sup.4 R.sup.5 is pyrrolidinyl, piperidyl or morpholyl, m is 1 or 2 and n is 2 to 6, are obtained by reacting 2 mols of an esterCH.sub.3 --CO--CH.sub.2 --CO--O--C.sub.n H.sub.2n+1-m (--NR.sup.4 R.sup.5).sub.m (2)with an aldehyde R.sup.3 --CHO (3). The compounds (1) easily saponify and decarboxylate without an added catalyst to form a cyclohexenones ##STR2## while setting free the alcoholHO--C.sub.n H.sub.2n+1-m (--NR.sup.4 R.sup.5).sub.m (5)which reacts without a catalyst with diketene to form the ester (2). Thus, in effect, 2 mols of diketene and 1 mol of aldehyde (3) form 1 mol of (4) and 2 mols of carbon dioxide as sole by-product. (4) can be transformed via the oxime to the correspondingly 5-substituted 3-methylaniline.

    摘要翻译: 环己酮和己烯酮其中A为R 1为氢或-CO-O-C n H 2n + 1-m(-NR 4 R 5)(1c)R 2为基团C 1,R 3为C 1 -C 10 - 烷基,苯基或被低级烷基,低级烷氧基,三氟甲基,硝基,氰基,氯代,氨基甲酰基,低级烷基 - 氨基甲酰基,氨磺酰基或低级烷基 - 氨磺酰基取代的苯基,R4和R5是低级烷基或-NR4R5是吡咯烷基, 或吗啉基,m为1或2,n为2至6,通过使2摩尔的酯CH3-CO-CH2-CO-O-CnH2n + 1-m(-NR4R5)m(2)与醛 R3-CHO(3)。 化合物(1)容易地皂化和脱羧而不加入催化剂以形成环己烯酮(4),同时游离醇,其中HO-CnH2n + 1-m(-NR4R5)m(5),其中没有催化剂与双烯酮反应 形成酯(2)。 因此,实际上,2摩尔双烯酮和1摩尔醛(3)形成1摩尔(4)和2摩尔二氧化碳作为副产物。 (4)可以通过肟转化为相应的5-取代的3-甲基苯胺。

    Process for the continuous preparation of aminoaryl or aminoalkyl
.beta.-sulfatoethyl sulfones
    6.
    发明授权
    Process for the continuous preparation of aminoaryl or aminoalkyl .beta.-sulfatoethyl sulfones 失效
    连续制备氨基芳基或氨基烷基β-磺基乙基砜的方法

    公开(公告)号:US5329040A

    公开(公告)日:1994-07-12

    申请号:US871341

    申请日:1992-04-21

    CPC分类号: C07C315/04

    摘要: In the process for the continuous preparation of aminoaryl or aminoalkyl .beta.-sulfatoethyl sulfones by reaction of the corresponding .beta.-hydroxyethyl sulfones with sulfuric acid in a molar ratio of 1:1 to 1:1.15 at temperatures above 120 .degree. C. a mixture of a .beta.-hydroxyethyl sulfone with sulfuric acid is supplied to a fluidized bed of end product produced by recycling and mechanical stirring. The mixture is reacted at 100.degree. to 200.degree. C.

    摘要翻译: 在连续制备氨基芳基或氨基烷基β-磺基乙基砜的过程中,通过相应的β-羟基乙基砜与硫酸在摩尔比为1:1至1:1.15的温度高于120℃下反应, 用硫酸将β-羟乙基砜供给到通过再循环和机械搅拌生产的最终产物的流化床。 混合物在100至200℃下反应

    Process for the preparation of aryldiazosulfonates
    9.
    发明授权
    Process for the preparation of aryldiazosulfonates 失效
    芳基二磺酸盐的制备方法

    公开(公告)号:US4515940A

    公开(公告)日:1985-05-07

    申请号:US391855

    申请日:1982-06-24

    申请人: Rudiger Berthold

    发明人: Rudiger Berthold

    CPC分类号: C07D235/26

    摘要: The invention relates to a process for the preparation of aryldiazosulfonates by reacting aqueous solutions of aryldiazonium salts with solutions or suspensions of sulfites, in particular in a manner such that the presence of an excess of one of the two reactants during the reaction is substantially excluded. The process according to the invention makes it possible substantially to increase the yields of aryldiazosulfonates.

    摘要翻译: 本发明涉及通过使芳基重氮盐的水溶液与亚硫酸盐的溶液或悬浮液反应制备芳基重氮磺酸盐的方法,特别是使得在反应期间基本排除了两种反应物中过量的一种反应物之一的存在。 根据本发明的方法使得可能基本上提高芳基二磺酸盐的产率。