PROCESS FOR PREPARING 2-OXINDOLE-1-CARBOXAMIDES
    83.
    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。

    A PROCESS FOR THE PRODUCTION OF 2,6-DIMETHYLDECALIN
    84.
    发明申请
    A PROCESS FOR THE PRODUCTION OF 2,6-DIMETHYLDECALIN 审中-公开
    一种生产2,6-二甲基环己烷的方法

    公开(公告)号:WO1993006067A1

    公开(公告)日:1993-04-01

    申请号:PCT/US1992008288

    申请日:1992-09-25

    Abstract: This invention is an acid catalyzed process for producing 2,6-dimethylnaphthaline from cyclohexyl compounds and naphthenic compounds or their precursors such as cyclohexane or methylcyclopentane, as depicted in the Figure. The cyclohexyl (10), cyclic alkane (12) stream and the catalyst (11) are fed into the reactor (14). After stripping of lighter ends, the product stream is passed to a heavy ends separation unit (28) and the product comprising primarily dimethyldecalins is recovered as the overhead stream (32). This stream may then be dehydrogenated to produce a dimethylnaphthalene stream (36) which may be subjected to a crystallization step (38) to produce reasonably pure 2,6-dimethylnaphthalene (40). The latter may optionally be oxidized to produce 2,6-dicarboxynaphthalene (44) suitable for polymerization to various polyester materials.

    Abstract translation: 本发明是由环己基化合物和环烷化合物或其前体如环己烷或甲基环戊烷生产2,6-二甲基萘的酸催化方法,如图所示。 将环己基(10),环烷烃(12)料流和催化剂(11)进料到反应器(14)中。 在汽提较轻的端部之后,将产物流送至重尾分离单元(28),并且主要包含二甲基十年总胆固醇的产物作为塔顶液流(32)回收。 然后可以将该物流脱氢以产生二甲基萘流(36),其可以进行结晶步骤(38)以产生合理纯的2,6-二甲基萘(40)。 后者可任选地被氧化以产生适于聚合成各种聚酯材料的2,6-二羧基萘(44)。

    PROCESS FOR PRODUCING BROMINE FROM BROMIDE SALTS
    85.
    发明申请
    PROCESS FOR PRODUCING BROMINE FROM BROMIDE SALTS 审中-公开
    从溴化钠生产溴的方法

    公开(公告)号:WO1993006039A1

    公开(公告)日:1993-04-01

    申请号:PCT/US1992007831

    申请日:1992-09-16

    CPC classification number: B01J27/08 B01J27/122 C01B7/096

    Abstract: This invention is a combination process for producing elemental bromine using bromide salt feedstocks. The process involves acidifying an inorganic bromide salt with a strong and concentrated acid, preferably sulfuric acid, to produce a gaseous HBr stream. The HBr stream is then mixed with an O2-containing gas and passed to an oxidation reactor where it is catalytically oxidized to produce a stream of Br2 and H2O. The hot reactor effluent is quenched and the product Br2 is separated from the H2O. In the figure, HBr stream is introduced into an evaporator (204) and to superheater (206). The O2 feedstream (208) is warmed. A reactor feedstream (214) is introduced into (216). The reaction product stream (218) is cooled in stages (220) and (222) and condensed. The condensate is then separated into a Br2 stream (224) added to water stream giving stream (226) and (228). The device (230) is a separator and (232) is a refrigeration unit. The resulting stream (234) is mixed with Br2 stream (224) giving noncondensed oxygen vapor stream (236) which is scrubbed in a gas treater (238). Distillation column (242) produces two streams (252) and (244). The overhead vapor stream (244) is condensed in overhead condenser (246) and collected in drum (248). The stream (250) is mixed with other streams. Device (256) is an absorption tower and (258) is the Br2 product stream.

    Abstract translation: 本发明是使用溴化物盐原料生产元素溴的组合方法。 该方法包括用强和浓酸(优选硫酸)酸化无机溴化物盐以产生气态HBr流。 然后将HBr流与含O2气体混合并通入氧化反应器,在其中进行催化氧化以产生Br 2和H 2 O流。 将热反应器流出物淬灭并将产物Br 2从H 2 O分离。 在该图中,将HBr流引入蒸发器(204)和过热器(206)中。 O2进料流(208)被加热。 将反应器进料流(214)引入(216)中。 反应产物流(218)分级(220)和(222)冷却并冷凝。 然后将冷凝物分离成添加到产生流(226)和(228)的水流中的Br 2流(224)。 设备(230)是分离器,(232)是制冷单元。 将所得流(234)与Br 2流(224)混合,得到在气体处理器(238)中洗涤的非冷凝氧蒸气流(236)。 蒸馏塔(242)产生两股料流(252)和(244)。 塔顶蒸气流(244)在塔顶冷凝器(246)中冷凝并收集在滚筒(248)中。 流(250)与其他流混合。 装置(256)是吸收塔,(258)是Br2产物流。

    CATALYST SYSTEM FOR OLEFIN OXIDATION TO CARBONYL PRODUCTS
    88.
    发明申请
    CATALYST 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剂体系

    公开(公告)号:WO1991013853A1

    公开(公告)日:1991-09-19

    申请号:PCT/US1991001515

    申请日:1991-03-05

    Inventor: CATALYTICA, INC.

    Abstract: The present invention provides reaction mixtures useful for oxidation of olefins to carbonyl products, comprising an olefin and an aqueous catalyst solution comprising a palladium catalyst, a polyoxoacid or polyoxoanion oxidant comprising vanadium, and dissolved olefin. It also provides processes for oxidation of olefins to carbonyl products, comprising mixing an olefin with an aqueous catalyst solution. It also provides processes for oxidation of olefins to carbonyl products by dioxygen, comprising mixing an olefin with an aqueous catalyst solution, and further comprising mixing dioxygen with the aqueous catalyst solution. In certain reaction mixtures and related processes of the present invention, the concentration of dissolved olefin in the aqueous catalyst solution is effective for its oxidation rate to not be limited by its rate of its diffusion into the aqueous solution. In other reaction mixtures and related processes of the present invention, the concentration of dissolved olefin in the aqueous catalyst solution is effective for its oxidation rate to be proportional to the palladium catalyst concentration. In other processes of the present invention, the olefin is mixed with the aqueous catalyst solution under mixing conditions effective for providing an olefin oxidation rate of at least 1 (millimole olefin/liter solution)/second. In other processes of the present invention, dioxygen is mixed with an aqueous reduced vanadium-polyoxoanion solution under mixing conditions effective for providing a dioxygen reaction rate of at least 1 (millimole dioxygen/liter solution)/second. In other reaction mixtures and related processes of the present invention, the aqueous solution is essentially free of sulfuric acid and sulfate ions.

    Abstract translation: 本发明提供了可用于将烯烃氧化成羰基产物的反应混合物,其包含烯烃和包含钯催化剂的含水催化剂溶液,包含钒和溶解烯烃的多氧酸或聚氧阴离子氧化剂。 它还提供了将烯烃氧化成羰基产物的方法,包括将烯烃与含水催化剂溶液混合。 它还提供了通过双氧将烯烃氧化成羰基产物的方法,包括将烯烃与催化剂水溶液混合,并且进一步包括将二氧化硅与催化剂水溶液混合。 在本发明的某些反应混合物和相关方法中,溶解的烯烃在催化剂水溶液中的浓度对于其氧化速率而言并不受其向水溶液中的扩散速度的限制而有效。 在本发明的其它反应混合物和相关方法中,溶解的烯烃在催化剂水溶液中的浓度对于其氧化速率与钯催化剂浓度成比例是有效的。 在本发明的其它方法中,烯烃与有效提供至少1(毫摩尔烯烃/升溶液)/秒的烯烃氧化速率的混合条件下与催化剂水溶液混合。 在本发明的其它方法中,在有效提供至少1(毫摩尔二氧/升溶液)/秒的双氧反应速率的混合条件下,将二氧化合物与含水还原型钒 - 多氧阴离子溶液混合。 在本发明的其它反应混合物和相关方法中,水溶液基本上不含硫酸和硫酸根离子。

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