3,11] dodecane. In this way, HBIW a quantity of bromine source and a co-solvent is charged to a reaction vessel. Palladium-based hydrogenation catalyst decomposition and acetic anhydride is added immediately to the reaction vessel. Hydrocracking catalyst should not contain substantially water. The reaction vessel for the conversion of tetra-acetyl-dibenzyl hexa A wood Seoul Tze Tan ("TADB") The HBIW, hydrogen is introduced rapidly removed and an atmosphere capable of reacting with the hydrogen from the reaction vessel. To have no time to form an acetylated derivative of acetic anhydride reacts with the HBIW prior to the start of the hydrogenation reaction of interest, acetic anhydride is added immediately prior to the introduction of hydrogen. In this way, very small amount, palladium-based catalyst of 10% weight / weight only less than is required by standard HBIW substrate preferably. Been subjected to use formic acid solvent, the hydrogenation process of the second in the presence of hydrogen tetra-acetyl-diformylphenol hexa A wood Seoul Tze Tan TADB which has precipitated in palladium-based hydrogenation decomposition on the catalyst, the ("TADF") form."/> 2,4,6,8,10,12, - the hexa- benzyl - 2,4,6,8,10,12 - hekisaazatetorashikuro 5.5.0.05, 9.03 and 11 hydrogenation resolution null 2,4,6,8,10,12 hexa- benzyl
首页> 外国专利> 2,4,6,8,10,12, - the hexa- benzyl - 2,4,6,8,10,12 - hekisaazatetorashikuro 5.5.0.05, 9.03 and 11 hydrogenation resolution null 2,4,6,8,10,12 hexa- benzyl

2,4,6,8,10,12, - the hexa- benzyl - 2,4,6,8,10,12 - hekisaazatetorashikuro 5.5.0.05, 9.03 and 11 hydrogenation resolution null 2,4,6,8,10,12 hexa- benzyl

机译:2,4,6,8,10,12,-六苄基-2,4,6,8,10,12-hekisaazatetorashikuro [5.5.0.05,9.03和11]氢化拆分无效2,4,6,8 ,10,12六苄基

摘要

(57) [summary] 2,4,6,8,10,12-hexa benzyl -2,4,6,8,10,12 hexaazatetracyclo [5.5.0.0 5,9 .0 water solution of ("HBIW") is disclosed 3,11] dodecane. In this way, HBIW a quantity of bromine source and a co-solvent is charged to a reaction vessel. Palladium-based hydrogenation catalyst decomposition and acetic anhydride is added immediately to the reaction vessel. Hydrocracking catalyst should not contain substantially water. The reaction vessel for the conversion of tetra-acetyl-dibenzyl hexa A wood Seoul Tze Tan ("TADB") The HBIW, hydrogen is introduced rapidly removed and an atmosphere capable of reacting with the hydrogen from the reaction vessel. To have no time to form an acetylated derivative of acetic anhydride reacts with the HBIW prior to the start of the hydrogenation reaction of interest, acetic anhydride is added immediately prior to the introduction of hydrogen. In this way, very small amount, palladium-based catalyst of 10% weight / weight only less than is required by standard HBIW substrate preferably. Been subjected to use formic acid solvent, the hydrogenation process of the second in the presence of hydrogen tetra-acetyl-diformylphenol hexa A wood Seoul Tze Tan TADB which has precipitated in palladium-based hydrogenation decomposition on the catalyst, the ("TADF") form.
机译:(57)[摘要] 2,4,6,8,10,12-六苄基-2,4,6,8,10,12六叠氮杂环[5.5.0.0 5,9 .0水 3,11] 十二烷公开了(“ HBIW”)的溶液。以此方式,将HBIW一定量的溴源和助溶剂装入反应容器中。将基于钯的氢化催化剂分解和乙酸酐立即添加到反应容器中。加氢裂化催化剂应基本不含水。用于转化四乙酰基-二苄基六氢A的木材的反应容器HTAW,氢气被快速除去,并且能够与来自反应容器的氢气反应的气氛被除去。为了没有时间形成乙酸酐的乙酰化衍生物,在感兴趣的氢化反应开始之前与HBIW反应,在加入氢之前立即添加乙酸酐。以此方式,非常少量的钯基催化剂优选地仅比标准HBIW基底所需的重量少10%重量/重量。在使用甲酸溶剂的条件下,第二次氢化过程是在氢四乙酰基-二甲酰基苯酚六氢六甲A的存在下进行的,该催化剂在钯基加氢分解催化剂上沉淀出,(“ TADF”)形成。

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