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    • 1. 发明申请
    • PROCESS FOR THE MANUFACTURE OF PROPYLENE OXIDE
    • 丙烯氧化物的制造工艺
    • US20120289722A1
    • 2012-11-15
    • US13512167
    • 2010-11-24
    • Prasad MuppaCaspar SchooldermanSandra Rens Van Der LeeRon Postma
    • Prasad MuppaCaspar SchooldermanSandra Rens Van Der LeeRon Postma
    • C07D301/12
    • C07D301/12Y02P20/52
    • A process for the manufacture of propylene oxide (“PO”) by catalytic oxidation of propylene with an oxidant wherein the catalytic oxidation is performed in an aqueous reaction medium, comprising water with less than 10% by volume of cosolvents, wherein a water-soluble manganese complex is used as oxidation catalyst,characterized in that the water-soluble manganese complex is a mononuclear species of the general formula (I): [LMnX3]Y   (I) or a binuclear species of the general formula (II): [LMn(μ-X)3MnL]Y2   (II) wherein Mn is a manganese; L or each L independently is a polydentate ligand, each X independently is a coordinating species and each μ-X independently is a bridging coordinating species, whereas Y is an non-coordinating counterion, and wherein the catalytic oxidation is carried out at a pH in the range of from 1.5 to 6.0.
    • 一种通过用氧化剂催化氧化丙烯来生产环氧丙烷(PO)的方法,其中催化氧化在水性反应介质中进行,其中包含少于10体积%共溶剂的水,其中水溶性锰络合物 用作氧化催化剂,其特征在于水溶性锰络合物是通式(I):[LMnX 3] Y(I)或通式(II)的双核物种的单核物种:[LMn(μ -X)3MnL] Y2(II)其中Mn是锰; L或每个L独立地是多齿配体,每个X独立地是配位物质,每个μ-X独立地是桥联配位物质,而Y是非配位抗衡离子,并且其中催化氧化在pH 范围从1.5到6.0。
    • 2. 发明授权
    • Process for the manufacture of propylene oxide
    • 制备环氧丙烷的方法
    • US08735613B2
    • 2014-05-27
    • US13512167
    • 2010-11-24
    • Prasad MuppaCaspar SchooldermanSandra Rens Van Der LeeRon Postma
    • Prasad MuppaCaspar SchooldermanSandra Rens Van Der LeeRon Postma
    • C07D301/12
    • C07D301/12Y02P20/52
    • A process for the manufacture of propylene oxide (“PO”) by catalytic oxidation of propylene with an oxidant wherein the catalytic oxidation is performed in an aqueous reaction medium, comprising water with less than 10% by volume of cosolvents, wherein a water-soluble manganese complex is used as oxidation catalyst,characterized in that the water-soluble manganese complex is a mononuclear species of the general formula (I): [LMnX3]Y   (I) or a binuclear species of the general formula (II): [LMn(μ-X)3MnL]Y2   (II) wherein Mn is a manganese; L or each L independently is a polydentate ligand, each X independently is a coordinating species and each μ-X independently is a bridging coordinating species, whereas Y is an non-coordinating counterion, and wherein the catalytic oxidation is carried out at a pH in the range of from 1.5 to 6.0.
    • 一种通过用氧化剂催化氧化丙烯来制备环氧丙烷(“PO”)的方法,其中催化氧化在含水反应介质中进行,其中含有小于10体积%共溶剂的水,其中水溶性 锰络合物用作氧化催化剂,其特征在于水溶性锰络合物是通式(I):[LMnX 3] Y(I)或通式(II)的双核物质的单核物质:[LMn (μ-X)3MnL] Y2(II)其中Mn是锰; L或每个L独立地是多齿配体,每个X独立地是配位物质,每个μ-X独立地是桥联配位物质,而Y是非配位抗衡离子,并且其中催化氧化在pH 范围从1.5到6.0。
    • 3. 发明申请
    • MANUFACTURE OF AN EPOXYETHYL ETHERS OR GLYCIDYL ETHERS
    • 环氧乙烷或甘油三酯的制备
    • US20120330041A1
    • 2012-12-27
    • US13574704
    • 2011-01-26
    • Prasad MuppaRon PostmaCaspar SchooldermanSandra RensKostas Stoitsas
    • Prasad MuppaRon PostmaCaspar SchooldermanSandra RensKostas Stoitsas
    • C07D301/12C07D301/03
    • C07D301/12
    • Processes are provided for the formation of an epoxyethyl ether or a glycidyl ether. In one embodiment, a process is provided for the manufacture of an epoxyethyl ether or glycidyl ether including reacting a vinyl ether or an allyl ether with an oxidant in the presence of a water-soluble manganese complex in an aqueous reaction medium, wherein the water-soluble manganese complex comprises an oxidation catalyst, characterized in that the water-soluble manganese complex is a mononuclear complex of the general formula (I): [LMnX3]Y (I), or a binuclear complex of the general formula (II): [LMn(μ-X)3MnL](Y)n (II), wherein Mn is a manganese; L or each L independently is a polydentate ligand, each X independently is a coordinating species and each μ-X independently is a bridging coordinating species, Y is a non-coordinating counter ion, and wherein the epoxidation is carried out at a pH in the range of from 1.0 to 6.0. The invention also relates to epoxyethyl ethers.
    • 提供了形成环氧乙醚或缩水甘油醚的方法。 在一个实施方案中,提供了制备环氧乙醚或缩水甘油醚的方法,包括在水性反应介质中在水溶性锰络合物存在下使乙烯基醚或烯丙基醚与氧化剂反应, 可溶性锰络合物包括氧化催化剂,其特征在于水溶性锰络合物是通式(I):[LMnX 3] Y(I)或通式(II)的双核络合物的单核络合物:[ LMn(μ-X)3MnL](Y)n(II),其中Mn是锰; L或每个L独立地是多齿配体,每个X独立地是配位物质,每个μ-X独立地是桥联配位物质,Y是非配位抗衡离子,并且其中环氧化在 范围从1.0到6.0。 本发明还涉及环氧乙醚。
    • 4. 发明授权
    • Manufacture of an epoxyethyl carboxylate or glycidyl carboxylate
    • 环氧乙基羧酸酯或羧酸缩水甘油酯的制备
    • US09174955B2
    • 2015-11-03
    • US13574693
    • 2011-01-26
    • Prasad MuppaRon PostmaCaspar SchooldermanSandra RensKostas Stoitsas
    • Prasad MuppaRon PostmaCaspar SchooldermanSandra RensKostas Stoitsas
    • C07D303/12C07D301/12C07D303/48
    • C07D301/12C07D303/48
    • The invention relates to a process for the manufacture of an epoxyethyl carboxylate or glycidyl carboxylate, including reacting a vinyl carboxylate or an allyl carboxylate using an oxidant and a water-soluble manganese complex in an aqueous reaction medium, and the water-soluble manganese complex comprises an oxidation catalyst, characterized in that the water-soluble manganese complex is a mononuclear species of the general formula (I) [LMnX3]Y (I), or a binuclear species of the general formula (II): [LMn(μ-X)3MnL]Yn (II), wherein Mn is a manganese; L is a ligand and each L is independently a polydentate ligand, each X is independently a coordinating species and each μ-X is independently a bridging coordinating species, Y is a non-coordinating counter ion, and wherein the epoxidation is carried out at a pH in the range of from 1.0 to 7.0.
    • 本发明涉及一种制备环氧乙基羧酸酯或缩水甘油羧酸酯的方法,包括在水性反应介质中使用氧化剂和水溶性锰络合物使羧酸乙烯酯或烯丙基羧酸酯反应,并且水溶性锰络合物包括 其特征在于所述水溶性锰络合物是通式(I)[LMnX 3] Y(I)的单核物种或通式(II)的双核物种:[LMn(μ-X )3MnL] Yn(II),其中Mn是锰; L是配体,每个L独立地是多齿配体,每个X独立地是配位物质,每个μ-X独立地是桥联配位物质,Y是非配位抗衡离子,其中环氧化在 pH范围为1.0-7.0。
    • 5. 发明授权
    • Manufacture of an epoxyethyl ethers or glycidyl ethers
    • 制备环氧乙醚或缩水甘油醚
    • US09145378B2
    • 2015-09-29
    • US13574704
    • 2011-01-26
    • Prasad MuppaRon PostmaCaspar SchooldermanSandra RensKostas Stoitsas
    • Prasad MuppaRon PostmaCaspar SchooldermanSandra RensKostas Stoitsas
    • C07D301/06C07D301/03C07D301/12
    • C07D301/12
    • Processes are provided for the formation of an epoxyethyl ether or a glycidyl ether. In one embodiment, a process is provided for the manufacture of an epoxyethyl ether or glycidyl ether including reacting a vinyl ether or an allyl ether with an oxidant in the presence of a water-soluble manganese complex in an aqueous reaction medium, wherein the water-soluble manganese complex comprises an oxidation catalyst, characterized in that the water-soluble manganese complex is a mononuclear complex of the general formula (I): [LMnX3]Y (I), or a binuclear complex of the general formula (II): [LMn(μ-X)3MnL](Y)n (II), wherein Mn is a manganese; L or each L independently is a polydentate ligand, each X independently is a coordinating species and each μ-X independently is a bridging coordinating species, Y is a non-coordinating counter ion, and wherein the epoxidation is carried out at a pH in the range of from 1.0 to 6.0. The invention also relates to epoxyethyl ethers.
    • 提供了形成环氧乙醚或缩水甘油醚的方法。 在一个实施方案中,提供了制备环氧乙醚或缩水甘油醚的方法,包括在水性反应介质中在水溶性锰络合物存在下使乙烯基醚或烯丙基醚与氧化剂反应, 可溶性锰络合物包括氧化催化剂,其特征在于水溶性锰络合物是通式(I):[LMnX 3] Y(I)或通式(II)的双核络合物的单核络合物:[ LMn(μ-X)3MnL](Y)n(II),其中Mn是锰; L或每个L独立地是多齿配体,每个X独立地是配位物质,每个μ-X独立地是桥联配位物质,Y是非配位抗衡离子,并且其中环氧化在 范围从1.0到6.0。 本发明还涉及环氧乙醚。