CATALYTIC SYSTEM FOR OLEFIN OXIDATION TO CARBONYL PRODUCTS
    35.
    发明申请
    CATALYTIC SYSTEM FOR OLEFIN OXIDATION TO CARBONYL PRODUCTS 审中-公开
    用于烯烃氧化成羰基产物的催化体系

    公开(公告)号:WO1991013851A1

    公开(公告)日:1991-09-19

    申请号:PCT/US1991001508

    申请日:1991-03-05

    Inventor: CATALYTICA, INC.

    Abstract: The present invention provides aqueous catalyst solutions useful for oxidation of olefins to carbonyl products, comprising a palladium catalyst, a polyoxoacid or polyoxoanion oxidant comprising vanadium, and chloride ions. It also provides processes for oxidation of olefins to carbonyl products, comprising contacting olefin with the aqueous catalyst solutions of the present invention. It also provides processes for oxidation of olefins to carbonyl products by dioxygen, comprising contacting olefin with the aqueous catalyst solutions of the present invention, and further comprising contacting dioxygen with the aqueous catalyst solutions. The present invention also provides a process for the oxidation of palladium (0) to palladium (II) comprising contacting the palladium (0) with an aqueous solution comprising chloride ions and a polyoxoacid or polyoxoanion oxidant comprising vanadium.

    Abstract translation: 本发明提供了用于将烯烃氧化成羰基产物的含水催化剂溶液,其包含钯催化剂,包含钒和氯离子的聚氧酸或聚氧化负离子氧化剂。 它还提供了将烯烃氧化成羰基产物的方法,包括使烯烃与本发明的含水催化剂溶液接触。 它还提供了通过双氧将烯烃氧化成羰基产物的方法,包括使烯烃与本发明的含水催化剂溶液接触,并且还包括使二氧化铈与含水催化剂溶液接触。 本发明还提供了将钯(0)氧化成钯(II)的方法,包括使钯(0)与包含氯离子的水溶液和包含钒的多氧酸或多氧阴离子氧化剂接触。

    PREPARATION OF PHOSPHOMOLYBDOVANADATE POLYOXOANIONS
    36.
    发明申请
    PREPARATION OF PHOSPHOMOLYBDOVANADATE POLYOXOANIONS 审中-公开
    磷酰胺多糖的制备

    公开(公告)号:WO1991013681A1

    公开(公告)日:1991-09-19

    申请号:PCT/US1991001517

    申请日:1991-03-05

    Inventor: CATALYTICA, INC.

    Abstract: The present invention provides a process for the preparation of acidic aqueous solutions consisting essentially of phosphomolybdovanadate salts. Certain processes of the present invention dissolve in water an oxide, oxoacid, or mixtures thereof, and at least one oxoanion salt of phosphorus, molybdenum, and vanadium, wherein the sum of salt cationic charges does not exceed the sum of the phosphomolybdovanadate anionic charges in the solution. Other processes of the present invention dissolve in water a) an oxide, oxoacid, oxoanion salt, or mixtures thereof of phosphorus, molybdenum, and vanadium and b) a carbonate salt, bicarbonate salt, hydroxide salt or mixtures thereof, wherein the sum of salt cationic charges does not exceed the sum of the phosphomolybdovanadate anionic charges in the solution. The present invention also provides processes for the preparation of solid phosphomolybdovanadate salts by evaporating the so produced aqueous solutions to recover essentially all the dissolved phosphomolybdovanadate salt in solid form.

    Abstract translation: 本发明提供了一种制备基本上由磷钼钒酸盐组成的酸性水溶液的方法。 本发明的某些方法在水中溶解氧化物,含氧酸或其混合物,以及磷,钼和钒的至少一种氧阴离子盐,其中盐阳离子电荷的总和不超过磷钼钒酸盐阴离子电荷的总和 解决方案。 本发明的其它方法溶解于水中a)氧,氧酸,氧代阴离子盐或其磷,钼和钒的混合物,和b)碳酸盐,碳酸氢盐,氢氧化物盐或其混合物,其中盐的总和 阳离子电荷不超过溶液中磷钼钒酸盐阴离子电荷的总和。 本发明还提供了通过蒸发所产生的水溶液来制备固体磷钼钒酸盐的方法,以基本上全部溶解固体形式的溶解的磷钼钒酸盐。

    PROCESS FOR PREPARING 2-OXINDOLE-1-CARBOXAMIDES
    40.
    发明申请
    PROCESS FOR PREPARING 2-OXINDOLE-1-CARBOXAMIDES 审中-公开
    制备2-氧杂-1-羧酰胺的方法

    公开(公告)号:WO1995020574A1

    公开(公告)日:1995-08-03

    申请号:PCT/US1995001005

    申请日:1995-01-27

    CPC classification number: C07D223/10 C07C273/1818 C07D209/34 C07C275/54

    Abstract: The present invention provides a process for preparing 2-oxindole-1-carboxamides, comprising reacting N-acyl 2-oxindole-1-carboxamides with alcohols in the presence of aprotic weak Lewis acid catalysts. In certain processes of the present invention a 2-oxindole-1-carboxamide is prepared from a 2-oxindole by reacting the 2-oxindole with an acyl isocyanate to produce the N-acyl 2-oxindole-1-carboxamide as an intermediate, which is then reacted with alcohol in the presence of aprotic weak Lewis acid catalysts. The N-acyl 2-oxindole-1-carboxamide intermediate may be converted to the 2-oxindole-1-carboxamide without isolation.

    Abstract translation: 本发明提供2-羟基吲哚-1-甲酰胺的制备方法,其包括在非质子弱路易斯酸催化剂存在下使N-酰基2-羟基吲哚-1-甲酰胺与醇反应。 在本发明的某些方法中,2-羟基吲哚-1-甲酰胺由2-羟基吲哚通过使2-羟基吲哚与酰基异氰酸酯反应制备N-酰基-2-羟基吲哚-1-甲酰胺作为中间体,其中 然后在非质子弱路易斯酸催化剂存在下与醇反应。 N-酰基2-羟基吲哚-1-甲酰胺中间体可以不分离地转化成2-羟基吲哚-1-甲酰胺。

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