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1. 发明授权

US06506952B2 Production of hexabromocyclododecane of enhanced gamma isomer content 失效
公开(公告)号：US06506952B2
公开(公告)日：2003-01-14
申请号：US09982708
申请日：2001-10-18
申请人： John K. Kendall
发明人： John K. Kendall
IPC分类号： C07C1702
CPC分类号： C07C17/02 , C07C23/02
摘要： Hexabromocyclododecane with enhanced gamma isomer content is produced by brominating cyclododecatriene in a liquid medium comprised of (1) at least 50 wt % of at least one liquid inert organic solvent other than 1,4-dioxane having a solubility in water of at least 1 wt % at 25° C., and (2) water in an amount of up to about 40 wt %, in the presence of (3) about 0.5 to about 30 wt % of bromide ion (Br−), each wt % being based on the total weight of the liquid portion of the liquid medium.

2. 发明授权

US06337425B1 Method for chlorinating ketones 失效
标题翻译：氯化酮的方法
公开(公告)号：US06337425B1
公开(公告)日：2002-01-08
申请号：US09646186
申请日：2000-09-14
申请人： Armin Stamm , Jochem Henkelmann
发明人： Armin Stamm , Jochem Henkelmann
IPC分类号： C07C1702
CPC分类号： C07C17/18 , C07C17/00 , C07C22/04 , C07C23/10 , C07C21/04 , C07C19/01
摘要： In a process for chlorinating ketones which, apart from the carbonyl group, are inert in respect of triarylphosphine dichlorides, except for cyclopropyl methyl ketone, in which the ketones are reacted with a chlorinating agent in the presence of triarylphosphine oxides, the amount of triarylphosphine oxide is from 0.1 to 10 mol %, based on the amount of ketone. The ketones preferably have a least one CH-acid proton in the &agr; position to the carbonyl group.
摘要翻译：在氯化酮的过程中，除了在三芳基氧化膦存在下酮与氯化剂反应的环丙基甲基酮以外，除了羰基外，它们是三芳基膦二氯化物是惰性的，三芳基氧化膦基于酮的量为0.1〜10摩尔％。酮优选在羰基的α位置具有至少一个CH-酸质子。

3. 发明授权

US06420617B1 Process for producing hexabromocyclododecane 有权
标题翻译：六溴环十二烷生产工艺
公开(公告)号：US06420617B1
公开(公告)日：2002-07-16
申请号：US09876902
申请日：2001-06-08
申请人： John K. Kendall , Jeffrey T. Aplin
发明人： John K. Kendall , Jeffrey T. Aplin
IPC分类号： C07C1702
CPC分类号： C07C17/02 , C07C23/02
摘要： This invention relates to the production of an hexabromocyclododecane product, which process comprises brominating cyclododecatriene in the presence of a 1,4-dioxane and water based solvent and from about 0.5 to about 30 wt % bromide ion in the liquid phase of the reaction mass. Optional post-reaction heat treatment in a finishing step increases process yields if needed. The hexabromocyclododecane product is unrecrystallized and contains no more than about 1.5 wt % tetrabromocyclododecene impurities.
摘要翻译：本发明涉及六溴环十二烷产物的制备，该方法包括在1,4-二恶烷和水基溶剂存在下溴化环十二碳三烯和在反应物料的液相中约0.5至约30重量％的溴离子。如果需要，在精加工步骤中可选的反应后热处理增加了工艺产量。六溴环十二烷产物是未再结晶的，并且含有不超过约1.5重量％的四溴环十二烷杂质。

4. 发明授权

US06252125B1 Process and unit for the production of 1,2-dichloroethane 有权
标题翻译：用于生产1,2-二氯乙烷的方法和单元
公开(公告)号：US06252125B1
公开(公告)日：2001-06-26
申请号：US09549682
申请日：2000-04-14
申请人： Peter Porscha
发明人： Peter Porscha
IPC分类号： C07C1702
CPC分类号： C07C17/02 , C07C17/383 , Y02P20/124 , Y02P20/51 , C07C19/045
摘要： By a process for the production of 1,2-dichloroethane (EDC) by reaction of ethylene with chlorine in the liquid phase (direct chlorination), the heavy ends being separated from the obtained 1,2-dichloroethane in a heavy-ends column and in a downstream vacuum column and, for the purpose of heat recovery and heating of the column bottoms, a 1,2-dichloroethane part-stream from the direct chlorination passing through a heat exchanger (one attributed to each column) for indirect heat exchange with the bottom product of each column, the aim of the invention is to provide a solution in which the reaction enthalpy of the direct chlorination can be used in a variable manner, thus precluding the above-described disadvantages. This is achieved by using at least one falling-film evaporator for heating the column bottoms, the bottom product of the respective column being routed to the distributor at the head of the column.
摘要翻译：通过在液相（直接氯化）中通过乙烯与氯的反应生产1,2-二氯乙烷（EDC）的方法，将重质末端与重馏分塔中的所得1,2-二氯乙烷分离，在下游真空塔中，为了塔底的热回收和加热，从直接氯化的1,2-二氯乙烷部分物流通过热交换器（一个归因于每个塔），用于与每列的底部产物，本发明的目的是提供一种溶液，其中可以以可变的方式使用直接氯化的反应焓，从而排除上述缺点。这通过使用至少一种用于加热柱底的降膜蒸发器，相应塔的底部产物被引导到塔顶部的分配器。

5. 发明授权

US06693224B1 Method and device for utilizing heat in the production of 1,2-dichloroethane 失效
标题翻译：在生产1,2-二氯乙烷时利用热量的方法和装置
公开(公告)号：US06693224B1
公开(公告)日：2004-02-17
申请号：US10070842
申请日：2002-05-22
申请人： Joachim Motz
发明人： Joachim Motz
IPC分类号： C07C1702
CPC分类号： C07C17/02 , Y02P20/123 , Y02P20/124 , Y02P20/51 , C07C19/045
摘要： The invention relates to a method for the production of 1,2-dichloroethane by direct chlorination using chlorine and ethene in which, despite low reaction temperatures during direct chlorination, reaction heat produced is nevertheless used. According to the invention, vaporous 1,2-dichloroethane obtained in the direct chlorination reactor is compressed and the compressed 1,2-dichloroethane is transported to heat exchangers whereby heat is given off by the 1,2-dichloroethane. The invention also relates to a device including a turbocompressor arranged directly after the direct chlorination reactor.
摘要翻译：本发明涉及使用氯和乙烯通过直接氯化生产1,2-二氯乙烷的方法，其中尽管在直接氯化期间反应温度低，但仍然使用所产生的反应热。根据本发明，在直接氯化反应器中获得的气态1,2-二氯乙烷被压缩，并将压缩的1,2-二氯乙烷输送到热交换器，由此由1,2-二氯乙烷发出热量。本发明还涉及一种包括直接排放在直接氯化反应器之后的涡轮压缩机的装置。

6. 发明授权

US06348634B1 Process for the (CFC-113a) dimerization 失效
标题翻译：（CFC-113a）二聚方法
公开(公告)号：US06348634B1
公开(公告)日：2002-02-19
申请号：US09496184
申请日：2000-02-02
申请人： Paolo Cuzzato , Ornella Majaron , Francesco Pinna
发明人： Paolo Cuzzato , Ornella Majaron , Francesco Pinna
IPC分类号： C07C1702
CPC分类号： C07C17/00 , B01J21/18 , B01J23/462 , B01J35/10 , C07C17/269 , C07C19/10 , C07C21/18
摘要： A reductive dimerization process of 1,1,1-trifluoro, 2,2,2-trichloroethane (CFC-113a) with hydrogen, with formation of 1,1,1,4,4,4-hexafluoro-2,2,3,3-tetrachlorobutane and 1,1,1,4,4,4-hexafluoro-2,2-dichlorobutene, and mixtures thereof, wherein the catalyst is constituted by metal ruthenium supported on graphitized carbon obtainable by treatment of the carbon at temperatures higher than 2000° C., in inert gas, or aluminum fluoride having an high surface area.
摘要翻译： 1,1,1-三氟，2,2,2-三氯乙烷（CFC-113a）与氢气的还原二聚过程，形成1,1,1,4,4,4-六氟-2,2,3 ，3-四氯丁烷和1,1,1,4,4,4-六氟-2,2-二氯丁烯及其混合物，其中催化剂由负载在石墨化碳上的金属钌构成，可通过在较高温度下处理碳获得超过2000℃，惰性气体或具有高表面积的氟化铝。

7. 发明授权

US06756513B2 Process for preparing monochlorinated hydrocarbons having a high isomeric purity 失效
标题翻译：具有高异构纯度的单氯代烃的方法
公开(公告)号：US06756513B2
公开(公告)日：2004-06-29
申请号：US10219289
申请日：2002-08-16
申请人： Manfred Neumann , Clemens Osterholt
发明人： Manfred Neumann , Clemens Osterholt
IPC分类号： C07C1702
CPC分类号： C07C17/16 , C07C22/04 , C07C19/01
摘要： Monochlorinated hydrocarbons of high isomeric purity are prepared by a process, which comprises: reacting a monoalcohol having an alkyl radical having from 3 to 20 carbon atoms with cyanuric chloride; and purifying the resulting monochlorinated hydrocarbon by distillation after separation of salts and washing the monochlorinated hydrocarbon with alkali. The invention relates to a process for preparing monochlorinated hydrocarbons which contain an alkyl radical having from 3 to 20 carbon atoms and have a high isomeric purity by reacting a monoalcohol having a hydrocarbon radical containing an alkyl radical having from 3 to 20 carbon atoms to which additional cycloaliphatic radicals, aryl radicals, aralkyl radicals and alkylaryl radicals may be bound with cyanuric chloride, separating off salts, washing the reaction mixture with alkali and purifying the resulting monochlorinated hydrocarbons by distillation.
摘要翻译：通过一种方法制备高异构纯度的一氯化烃，该方法包括：使具有3-20个碳原子的烷基的一元醇与氰尿酰氯反应; 并在分离盐后通过蒸馏对所得一氯化烃进行纯化，并用碱洗涤一氯化烃。本发明涉及一种制备含有具有3至20个碳原子并具有高异构纯度的单氯代烃的方法，其通过使具有含有具有3至20个碳原子的烷基的烃基的一元醇，其中另外的脂环族基团，芳基，芳烷基和烷基芳基可以与氰尿酰氯结合，分离出盐，用碱洗涤反应混合物并纯化通过蒸馏得到单氯化烃。

8. 发明授权

US06528693B1 Preparation of cyclopropylethyne and intermediates for preparation of cyclopropylethyne 失效
标题翻译：环丙基乙炔和制备环丙基乙炔的中间体的制备
公开(公告)号：US06528693B1
公开(公告)日：2003-03-04
申请号：US09806980
申请日：2001-04-05
申请人： Robert Gandy , Peter John Cremins , Allan Williams Timms
发明人： Robert Gandy , Peter John Cremins , Allan Williams Timms
IPC分类号： C07C1702
CPC分类号： C07F9/535 , C07C1/30 , C07C13/04 , C07C17/00 , C07C2601/02 , C07C22/00
摘要： 1-chloropropylethyne is prepared by dehydrochlorination with a base of 1-chloro-1-cyclopropylethene, which is itself prepared by treating 1-cyclopropylethanone with dichlorotriarylphosphorane or dichlorotrialkylphosphorane in the presence of a base.
摘要翻译： 1-氯丙基乙炔通过用1-氯-1-环戊烯的碱脱氯化氢来制备，其本身是通过在碱的存在下用二氯三芳基磷烷或二氯三烷基磷烷处理1-环丙基乙酮来制备的。

9. 发明授权

US06403848B1 Preparation of hexafluoropropylene from the pyrolysis of trifluoromethane and tetrafluoroethylene 失效
标题翻译：从三氟甲烷和四氟乙烯的热解制备六氟丙烯
公开(公告)号：US06403848B1
公开(公告)日：2002-06-11
申请号：US09820631
申请日：2001-03-30
申请人： Dong Ju Moon , Hong Gon Kim , Byoung Sung Ahn , Moon Jo Chung , Young Soo Kwon
发明人： Dong Ju Moon , Hong Gon Kim , Byoung Sung Ahn , Moon Jo Chung , Young Soo Kwon
IPC分类号： C07C1702
CPC分类号： C07C17/269 , C07C21/18
摘要： The present invention relates to a process for preparing hexafluoropropylene(CF3CF═CF2, HFP) from the pyrolysis of trifluoromethane(CHF3, R23) and tetrafluoroethylene(C2F4, TFE) and more particularly, to the process for preparing hexafluoropropylene from the pyrolysis of an admixture of R23 and TFE mixed in an appropriate molar ratio at below 900 which is lower than the conventional reaction temperature and longer residence time, after investigating the pyrolysis reaction of R23 and TFE by the computer simulation. The process for preparing HFP is performed by carefully controlling reaction temperature with heat balance resulted from an endothermic pyrolysis of R23 and an exothermic dimerization of TFE to prevent from carbon formation, recycling unreacted R23 and TFE in the product separated and purified from distillation column, adding fresh R23 additionally to keep an appropriate molar ratio of R23 and TFE, to improve a total yield of HFP and to minimize heat supply from outside.
摘要翻译：本发明涉及从三氟甲烷（CHF 3，R 23）和四氟乙烯（C 2 F 4，TFE）的热解制备六氟丙烯（CF 3 CF = CF 2，HFP）的方法，更具体地说，涉及从混合物的热解制备六氟丙烯的方法通过计算机模拟研究R23和TFE的热解反应后，R23和TFE以适合的摩尔比混合在900以下，低于常规反应温度和较长的停留时间。制备HFP的过程是通过仔细控制反应温度和由R23的吸热热解产生的热平衡和TFE的放热二聚反应来防止形成碳，循环未反应的R23和TFE，从蒸馏塔中分离和纯化，加入新鲜的R23另外保持适当的R23和TFE的摩尔比，以提高HFP的总产率并最小化从外部的供热。

10. 发明授权

US06291731B1 Continuous method for producing propargyl chloride 失效
标题翻译：产生炔丙基氯的连续方法
公开(公告)号：US06291731B1
公开(公告)日：2001-09-18
申请号：US09623171
申请日：2000-08-29
申请人： Armin Stamm , Jochem Henkelmann , Hans-Jürgen Weyer
发明人： Armin Stamm , Jochem Henkelmann , Hans-Jürgen Weyer
IPC分类号： C07C1702
CPC分类号： C07C17/16 , C07C21/22
摘要： In a continuous process for preparing propargyl chloride by reacting propargyl alcohol with a chlorinating agent in the presence of a catalyst, the chlorinating agent, propargyl alcohol and from 0.1 to 10 mol % of the catalyst, based on the amount of propargyl alcohol, are continuously metered into a reaction zone and reacted at from 40 to 70° C.
摘要翻译：在催化剂存在下，通过炔丙醇与氯化剂反应来制备炔丙基氯的连续方法中，氯化剂炔丙醇和基于炔丙醇的量为0.1-10mol％的催化剂是连续的计量加入反应区，并在40〜70℃反应

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