利索-全球专利检索

  1. 登录
  2. 注册

搜索结果

28 条记录 (耗时 0.025 秒)

    Method for preparing formylphosphonic acid
    4.
    发明授权
    Method for preparing formylphosphonic acid 有权

    公开(公告)号：US07091376B2

    公开(公告)日：2006-08-15

    申请号：US10868236

    申请日：2004-06-15

    申请人： Thaddeus S. Franczyk, II

    发明人： Thaddeus S. Franczyk, II

    IPC分类号： C07F9/22 ,  C07F9/28

    CPC分类号： C07F9/3891 ,  C07F9/3813 ,  C07F9/3817

    摘要： An improved process for the manufacture of formylphosphonic acid derivatives is reported. An aminomethylphosphonic acid substrate is contacted with a reagent selected from the group consisting of water, an alcohol, a phenol compound, and mixtures thereof and an oxidizing gas in the presence of a catalyst to form a reaction product mixture containing a formylphosphonic acid derivative and the conditions under which said contacting is carried out are controlled so that no more than 50% of the formylphosphonic acid derivative formed in the reaction product mixture is consumed by reaction with the reagent.

    Process for the preparation of carboxylic acid salts from primary alcohols
    6.
    发明授权
    Process for the preparation of carboxylic acid salts from primary alcohols 失效
    从伯醇制备羧酸盐的方法

    公开(公告)号：US06646160B2

    公开(公告)日：2003-11-11

    申请号：US09563683

    申请日：2000-05-03

    申请人： Thaddeus S. Franczyk, II ,  William L. Moench, Jr.

    发明人： Thaddeus S. Franczyk, II ,  William L. Moench, Jr.

    IPC分类号： C07C51291

    CPC分类号： C07C227/02 ,  C07C229/08 ,  C07C229/12 ,  C07C229/16

    摘要： The present invention provides a new and useful improvement in the process to manufacture a carboxylic acid salt, particularly an amino carboxylic acid salt, from a primary alcohol, particularly a primary aminoalcohol. The process of manufacturing amino carboxylic acid salts comprises contacting an aqueous solution of a primary aminoalcohol with a strong hydroxide base selected from the group consisting of an alkali metal hydroxide, an alkaline earth metal hydroxide, an ammonium hydroxide compound including a tetraalkyl ammonium hydroxide, or the like, in the presence of an effective amount of a catalyst. The catalyst comprises one or more of elements selected from the group consisting of copper, cobalt, nickel, and cadmium as well as optionally lesser amounts of chromium, titanium, niobium, tantalum, zirconium, vanadium, molybdenum, manganese, tungsten, cobalt, nickel, or mixtures thereof. The reaction mixture contains less than about 3000 ppm, preferably less than about 500 ppm, more preferably less than about 100 ppm of oxidized copper (Cu+ and/or Cu2+) during the reaction. The concentration of oxidizing agents in the reactants is minimized to prevent formation of oxidized copper from metallic copper catalyst.

    摘要翻译： 本发明提供了从伯醇，特别是伯氨基醇制备羧酸盐，特别是氨基羧酸盐的方法中的新的和有用的改进。 制备氨基羧酸盐的方法包括将伯氨基醇的水溶液与选自碱金属氢氧化物，碱土金属氢氧化物，氢氧化铵，氢氧化四烷基铵或氢氧化四烷基铵的强氢氧化物碱 在有效量的催化剂存在下进行。 催化剂包含一种或多种选自铜，钴，镍和镉的元素，以及任选少量的铬，钛，铌，钽，锆，钒，钼，锰，钨，钴，镍 ，或其混合物。 反应混合物在反应期间含有小于约3000ppm，优选小于约500ppm，更优选小于约100ppm的氧化铜（Cu 2+和/或Cu 2+）。 反应物中氧化剂的浓度被最小化以防止金属铜催化剂形成氧化铜。

    Continuous process for the preparation of N-(phosphonomethyl)iminodiacetic acid
    7.
    发明授权
    Continuous process for the preparation of N-(phosphonomethyl)iminodiacetic acid 有权
    连续制备N-（膦酰基甲基）亚氨基二乙酸的方法

    公开(公告)号：US06278017B1

    公开(公告)日：2001-08-21

    申请号：US09612705

    申请日：2000-07-10

    申请人： Michael K. Stern ,  Todd J. Johnson ,  Amy L. Jorgenson ,  Michael D. Rogers ,  Thaddeus S. Franczyk, II

    发明人： Michael K. Stern ,  Todd J. Johnson ,  Amy L. Jorgenson ,  Michael D. Rogers ,  Thaddeus S. Franczyk, II

    IPC分类号： C07F938

    CPC分类号： C07D241/08 ,  C07C233/47 ,  C07F9/3808

    摘要： A process for the continuous production of N-(phosphonomethyl)glycine is provided. In the process, N-(acetyl)iminodiacetic acid is formed in an amidocarboxymethylation reactor system. The N-(acetyl)iminodiacetic acid product stream is either: (1) reacted with a source of phosphorous and a source of formaldehyde in the presence of an acid to form a phosphonomethylation reaction product stream containing N-(phosphonomethyl)iminodiacetic acid and acetic acid; or (2) deacylated and cyclized to form a 2,5-diketopiperazine, and then reacted with a source of phosphorous and a source of formaldehyde in the presence of an acid to form a phosphonomethylation reaction product stream containing N-(phosphonomethyl)iminodiacetic acid and acetic acid. In either case, the N-(phosphonomethyl)iminodiacetic acid product is recovered and converted to N-(phosphonomethyl)glycine.

    摘要翻译： 提供了连续生产N-（膦酰基甲基）甘氨酸的方法。 在此过程中，N-（乙酰基）亚氨基二乙酸在酰胺羧甲基化反应器体系中形成。 N-（乙酰基）亚氨基二乙酸产物流是：（1）在酸存在下与磷源和甲醛源反应，形成含有N-（膦酰基甲基）亚氨基二乙酸和乙酸的膦酰基甲基化反应产物流 酸; 或（2）脱酰基并环化形成2,5-二酮哌嗪，然后在酸存在下与磷源和甲醛源反应，形成含有N-（膦酰基甲基）亚氨基二乙酸的膦酰基甲基化反应产物流 和乙酸。 在任一种情况下，N-（膦酰基甲基）亚氨基二乙酸产物被回收并转化成N-（膦酰基甲基）甘氨酸。

    Method for preparing formylphosphonic acid
    9.
    发明授权
    Method for preparing formylphosphonic acid 有权
    甲酰膦酸的制备方法

    公开(公告)号：US07294733B2

    公开(公告)日：2007-11-13

    申请号：US11422256

    申请日：2006-06-05

    申请人： Thaddeus S. Franczyk, II

    发明人： Thaddeus S. Franczyk, II

    IPC分类号： C07F9/22 ,  C07F9/30 ,  C07F9/32

    CPC分类号： C07F9/3891 ,  C07F9/3813 ,  C07F9/3817

    摘要： An improved process for the manufacture of formylphosphonic acid derivatives is reported. An aminomethylphosphonic acid substrate is contacted with a reagent selected from the group consisting of water, an alcohol, a phenol compound, and mixtures thereof and an oxidizing gas in the presence of a catalyst to form a reaction product mixture containing a formylphosphonic acid derivative and the conditions under which said contacting is carried out are controlled so that no more than 50% of the formylphosphonic acid derivative formed in the reaction product mixture is consumed by reaction with the reagent.

    摘要翻译： 报道了制备甲酰基膦酸衍生物的改进方法。 使氨基甲基膦酸底物与选自水，醇，酚化合物及其混合物的试剂和氧化气体在催化剂存在下接触以形成含有甲酰基膦酸衍生物和 控制进行所述接触的条件，使得反应产物混合物中形成的甲酰基膦酸衍生物不超过50％被与试剂反应消耗。

    Method of making phosphorus-containing compounds and products thereof
    10.
    发明授权
    Method of making phosphorus-containing compounds and products thereof 有权
    制造含磷化合物及其制品的方法

    公开(公告)号：US06864218B2

    公开(公告)日：2005-03-08

    申请号：US10192709

    申请日：2002-07-09

    申请人： Thaddeus S. Franczyk, II

    发明人： Thaddeus S. Franczyk, II

    IPC分类号： C07F9/38 ,  C07F9/40 ,  A01N57/18 ,  C07C9/22 ,  C07F9/02

    CPC分类号： C07F9/4065 ,  C07F9/3813 ,  C07F9/3891 ,  C07F9/4006

    摘要： A process for oxidizing a hydroxymethylphosphonic acid compound to produce a formylphosphonic acid compound is described. The oxidation reaction is carried out in the presence of an oxidant and a catalyst. For example, hydroxymethylphosphonic acid (HMPA) is oxidized by oxygen or hydrogen peroxide in the presence of a copper-containing catalyst to give formylphosphonic acid (FPA). Formylphosphonic acid can then be reacted with glycine to produce a condensation product which, upon hydrogenation, yields glyphosate. Glyphosate can be incorporated into various formulations for use as a herbicide. In addition to glycine, formylphosphonic acid can also be reacted with ammonia, ethanolamine, or other primary amines to form a precursor compound, which can be converted to glyphosate.

    摘要翻译： 描述了氧化羟甲基膦酸化合物以产生甲酰膦酸化合物的方法。 氧化反应在氧化剂和催化剂的存在下进行。 例如，羟基甲基膦酸（HMPA）在含铜催化剂存在下被氧或过氧化氢氧化，得到甲酰基膦酸（FPA）。 然后可以将甲基膦酸与甘氨酸反应以产生缩合产物，其在氢化时产生草甘膦。 草甘膦可以并入用作除草剂的各种制剂中。 除了甘氨酸之外，甲酰基膦酸还可以与氨，乙醇胺或其它伯胺反应形成前体化合物，其可以转化成草甘膦。