Preparation of isocyanates
    33.
    发明授权
    Preparation of isocyanates 失效
    异氰酸酯的制备

    公开(公告)号:US4322365A

    公开(公告)日:1982-03-30

    申请号:US265156

    申请日:1981-05-19

    CPC分类号: C07C263/12

    摘要: Isocyanates are prepared by thermal decomposition of oxalic acid ester amides at not less than 300.degree. C.The isocyanates obtainable by the process of the invention are valuable starting materials for the preparation of crop protection agents, pesticides, dyes, synthetic resins, plastics, textile waterproofing agents, detergents and adhesives.

    摘要翻译: 异氰酸酯是通过不低于300℃的草酸酯酰胺的热分解制备的。通过本发明的方法可获得的异氰酸酯是用于制备作物保护剂,农药,染料,合成树脂,塑料,纺织品的有价值的起始材料 防水剂,洗涤剂和粘合剂。

    Process for recycling noble metal catalysts used for the manufacture of
aromatic urethanes
    34.
    发明授权
    Process for recycling noble metal catalysts used for the manufacture of aromatic urethanes 失效
    回收用于制造芳族聚氨酯的贵金属催化剂的方法

    公开(公告)号:US4319035A

    公开(公告)日:1982-03-09

    申请号:US207057

    申请日:1980-11-10

    CPC分类号: B01J27/32

    摘要: A process for the preparation of an aromatic urethane by the reaction in solution of an aromatic nitro compound or aromatic amine in the presence of an oxidation agent, with a hydroxyl compound and carbon monoxide in the presence of a noble metal catalyst, the improvement which comprises (a) treating the reaction solution, containing the noble metal catalyst, after the urethane formation is complete, with hydrogen (b) separating the noble metal in elementary form from the reaction solution, and (c) reusing the noble metal, together with a hydrohalic acid, as a catalyst.

    摘要翻译: 在贵金属催化剂存在下,通过芳族硝基化合物或芳族胺在氧化剂存在下与羟基化合物和一氧化碳的溶液中的反应制备芳族氨基甲酸酯的方法,其改进包括 (a)在氨基甲酸酯化形成完成后,用氢(b)将基本形式的贵金属与反应溶液分离,处理包含贵金属催化剂的反应溶液,(c)将贵金属与 氢卤酸,作为催化剂。

    Preparation of 3-hydroxy-2,2,4-trimethylpentyl isobutyrate
    36.
    发明授权
    Preparation of 3-hydroxy-2,2,4-trimethylpentyl isobutyrate 失效
    制备3-羟基-2,2,4-三甲基戊基异丁酸酯

    公开(公告)号:US4273934A

    公开(公告)日:1981-06-16

    申请号:US31013

    申请日:1979-04-17

    CPC分类号: C07C67/44

    摘要: 3-Hydroxy-2,2,4-trimethylpentyl isobutyrate is prepared by reaction of isobutyraldehyde in the presence of an alkaline earth metal hydroxide and of carboxylic acids or the corresponding salts, under specific conditions in respect of reaction time and proportion and concentration of the hydroxide suspension. The product is a starting material for the preparation of dyes, pesticides, adhesives and surface coatings.

    摘要翻译: 3-羟基-2,2,4-三甲基戊基异丁酸酯通过异丁醛在碱土金属氢氧化物和羧酸或相应的盐的存在下,在特定条件下,在反应时间和比例和浓度 氢氧化物悬浮液。 该产品是制备染料,农药,粘合剂和表面涂料的起始原料。

    Preparation of 4-acetoxystyrene
    39.
    发明授权
    Preparation of 4-acetoxystyrene 失效
    4-乙酰氧基苯乙烯的制备

    公开(公告)号:US5380918A

    公开(公告)日:1995-01-10

    申请号:US126880

    申请日:1993-09-27

    IPC分类号: C07C67/297 C07C69/157

    CPC分类号: C07C67/297

    摘要: 4-Acetoxystyrene of the formula I ##STR1## is prepared by a process in which a 1-(4-acetoxyphenyl)ethyl carboxylate of the formula II ##STR2## where R is C.sub.1 -C.sub.10 -alkyl, C.sub.3 -C.sub.6 -cycloalkyl, aryl or C.sub.7 -C.sub.10 -aralkyl, is converted in the presence of an acidic catalyst and of a polymerization inhibitor in an inert heat transfer medium at from 160.degree. to 250.degree. C. and from 0.1 to 300 mbar.

    摘要翻译: 通式Ⅰ(I)的4-乙酰氧基苯乙烯通过以下方法制备:其中R为C 1 -C 10 - 烷基,C 3 -C 6烷基的式(II)的1-(4-乙酰氧基苯基)乙基羧酸酯 -C 1-6 - 环烷基,芳基或C 7 -C 10 - 芳烷基在惰性传热介质中在酸性催化剂和阻聚剂的存在下在160-250℃和0.1至300毫巴条件下转化。

    Preparation of 3-aminomethyl-3,5,5-trimethyl-cyclohexylamine
    40.
    发明授权
    Preparation of 3-aminomethyl-3,5,5-trimethyl-cyclohexylamine 失效
    3-氨基甲基-3,5,5-三甲基 - 环己胺的制备

    公开(公告)号:US5371292A

    公开(公告)日:1994-12-06

    申请号:US92029

    申请日:1993-07-15

    摘要: A process for the preparation of 3-aminomethyl-3,5,5-trimethyl-cyclohexylamine from 3-cyano-3,5,5-trimethyl-cyclohexanone, wherein the following stages are carried out in discrete reaction chambers:a) the 3-cyano-3,5,5-trimethyl-cyclohexanone is reacted in a first reaction chamber with excess ammonia over an acidic metal oxide catalyst at a temperature of from 20.degree. to 150.degree. C. and a pressure of from 15 to 500 bar, andb) in a second reaction chamber, the reaction product from stage a) is hydrogenated with hydrogen at a temperature of from 60.degree. to 150.degree. C. and a pressure of from 50 to 300 bar in the presence of excess ammonia over a catalyst containing cobalt, nickel, ruthenium, and/or some other noble metal, which catalyst optionally contains a basic component or is supported by neutral or basic supporting material.

    摘要翻译: 从3-氰基-3,5,5-三甲基 - 环己酮制备3-氨基甲基-3,5,5-三甲基 - 环己胺的方法,其中以下步骤在离散反应室中进行:a)3 氰基-3,5,5-三甲基 - 环己酮在第一反应室中与过量的氨在酸性金属氧化物催化剂上在20至150℃的温度和15至500巴的压力下反应, 和b)在第二反应室中,在过量的氨在催化剂存在下,将氢气从60℃升至150℃,压力为50-300巴,在步骤a)中的反应产物被氢化 含有钴,镍,钌和/或一些其它贵金属,该催化剂任选地含有碱性组分或由中性或碱性载体材料负载。