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    • 44. 发明授权
    • Process for production of iodine compounds and process for production of high-purity 5-iodo-2-methylbenzoic acid
    • 生产碘化合物的方法和生产高纯度5-碘-2-甲基苯甲酸的方法
    • US07750182B2
    • 2010-07-06
    • US10545005
    • 2004-02-10
    • Toshio HidakaTakafumi YoshimuraYoshifumi SatoNorio FushimiMasaharu Doya
    • Toshio HidakaTakafumi YoshimuraYoshifumi SatoNorio FushimiMasaharu Doya
    • C07C17/00C07C63/04
    • C07C253/30C07B39/00C07C17/12C07C17/156C07C17/158C07C51/363C07C51/43C07C25/02C07C25/13C07C25/18C07C25/125C07C63/70C07C255/50
    • Provided is a production method for an iodine compound in which iodine is reacted with a substrate in the presence of a porous material having a pore diameter of 500 nm or less or in the presence of the above porous material and an oxidizing agent and a production process for high purity 5-iodo-2-methylbenzoic acid comprising an iodination reaction step carried out by the above-mentioned, a crystal precipitation and separation step in which a product is precipitated by adding water or cooling and then separated and a purification step in which crystal separated is recrystallized using an organic solvent. According to the production method for an iodine compound described above, iodine can be introduced into various substrates at a high selectivity. Since expensive metals and specific reagents do not have to be used, it can readily be carried out in an industrially scale, and the product having a high purity can be obtained. Further, the process comprising the iodination reaction, separation and purification steps described above makes it possible to readily obtain at a high yield, 5-iodo-2-methylbenzoic acid having a high purity which is useful in uses for functional chemical products such as medicines. The process of the present invention comprising iodination reaction, separation and purification steps is characterized by that it is simple in terms of a procedure and that the purification load is smaller, and it is very advantageous in industrially carrying out.
    • 提供一种碘化合物的制造方法,其中碘在孔径为500nm以下的多孔质材料的存在下,或者在上述多孔质材料和氧化剂的存在下,与基材反应,制造方法 包括通过上述进行的碘化反应步骤的高纯度5-碘-2-甲基苯甲酸,其中通过加入水或冷却然后分离产物而沉淀产物的晶体沉淀和分离步骤和纯化步骤,其中 使用有机溶剂重结晶晶体分离。 根据上述碘化合物的制造方法,能够以高选择性将碘引入各种基材中。 由于不需要使用昂贵的金属和特定试剂,因此可以容易地以工业规模进行,可以获得高纯度的产物。 此外,包括上述碘化反应,分离和纯化步骤的方法使得可以容易地以高产率获得具有高纯度的5-碘-2-甲基苯甲酸,其可用于诸如药物的功能性化学产品的用途 。 包括碘化反应,分离和纯化步骤的本发明方法的特征在于它在程序方面简单,净化负荷较小,在工业上非常有利。
    • 49. 发明授权
    • Processes for geometric isomerization of halogenated olefins
    • 卤代烯烃几何异构化方法
    • US07563936B2
    • 2009-07-21
    • US11588466
    • 2006-10-27
    • Haiyou WangHsueh Sung Tung
    • Haiyou WangHsueh Sung Tung
    • C07C17/00
    • C07C17/358C07C21/18
    • Disclosed are processes for the conversion of isomerizable halogenated C2-C6 olefins from one geometric form to a more preferred geometric form. Preferred process aspects involve converting C2-C6 olefin in a cis-form to a trans-form under conditions effective to convert at least about 50 percent, and even more preferably at least about 70 percent, of the cis-form compound to the trans-form compound. In preferred embodiments the C2-C6 olefin comprises tetrafluoropropene, with cis-1,3,3,3 tetrafluoropropene (cis-HFO-1234ze) being converted, preferably at high conversion rates and high selectivity, to trans-1,3,3,3 tetrafluoropropene (trans-HFO-1234ze). In preferred embodiments the conditions effective to achieve the desired high levels of conversion and selectivity include exposing the feed to a metal based catalyst selected from the group consisting of halogentated metal oxides, Lewis acid metal halides, zero-valent metals, and combinations of these, preferably under reaction conditions, including reaction temperature and residence time, effective to convert at least about 5% of the cis-form of the compound to other compounds and to further achieve a selectivity to the trans-form of the compound of at least about 70%.
    • 公开了将可异构化的卤代C 2 -C 6烯烃从一种几何形式转化为更优选的几何形式的方法。 优选的方法方面涉及在有效将至少约50%,甚至更优选至少约70%的顺式形式化合物转化成反式 - 形式的条件下,将顺式C2-C6烯烃转化为反式 - 形成化合物。 在优选的实施方案中,C2-C6烯烃包括四氟丙烯,顺式-1,3,3,3四氟丙烯(顺式-HFO-1234ze)优选以高转化率和高选择性转化成反式1,3,3,3-四氟丙烯, 3四氟丙烯(反式HFO-1234ze)。 在优选的实施方案中,有效实现期望的高水平转化率和选择性的条件包括将进料暴露于金属基催化剂中,所述催化剂选自卤化金属氧化物,路易斯酸金属卤化物,零价金属及其组合, 优选在反应条件下,包括反应温度和停留时间,有效地将至少约5%的顺式化合物转化为其它化合物,并进一步实现化合物的反式形式至少约70的选择性 %。