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    TWO-STAGE METHOD FOR PRODUCING BUTANDIOL IN TWO REACTORS
    2.
    发明申请
    TWO-STAGE METHOD FOR PRODUCING BUTANDIOL IN TWO REACTORS 审中-公开
    两步反应器制备丁醇的两步法

    公开(公告)号：WO03104214A8

    公开(公告)日：2004-05-13

    申请号：PCT/EP0306060

    申请日：2003-06-10

    Applicant: BASF AG ,  HESSE MICHAEL ,  SCHLITTER STEPHAN ,  BORCHERT HOLGER ,  SCHUBERT MARKUS ,  ROESCH MARKUS ,  BOTTKE NILS ,  FISCHER ROLF-HARTMUTH ,  WECK ALEXANDER ,  WINDECKER GUNTHER ,  HEYDRICH GUNNAR

    Inventor： HESSE MICHAEL ,  SCHLITTER STEPHAN ,  BORCHERT HOLGER ,  SCHUBERT MARKUS ,  ROESCH MARKUS ,  BOTTKE NILS ,  FISCHER ROLF-HARTMUTH ,  WECK ALEXANDER ,  WINDECKER GUNTHER ,  HEYDRICH GUNNAR

    IPC: C07C29/149 ,  C07D315/00 ,  C07C31/20 ,  C07D307/20

    CPC classification number: C07D315/00 ,  C07C29/149 ,  C07C31/207

    Abstract: The invention relates to a method for producing optionally akyl-substituted 1,4-butandiol by two-stage catalytic hydration in the gaseous phase of C4 dicarboxylic acids and/or the derivatives thereof with the steps of: a) introducing a gaseous flow of a C4 dicarboxylic acid or a derivative thereof at 200 to 300 °C and 2 to 60 bar in a first reactor and catalytic gas phase hydration to a mainly optionally alkyl-substituted gamma-butyrolactone containing product; b) introducing the product flow so obtained into a second reactor at a temperature of from 150 °C to 240 °C and a pressure of from 15 to 100 bar and catalytic gas phase hydration to optionally alkyl-substituted 1,4-butandiol; c) removing the desired product from the intermediates, byproducts and possibly not reacted educt; d) optionally returning non-reacted intermediates to one or both hydration stages, whereby in both hydration stages one catalyst each is used which comprises = 5 % by weight, preferably 5 to 95 % by weight, especially 20 to 90 % by weight of an oxidic carrier, the pressure prevailing in the second reactor is higher than in the first reactor, and the product mixture removed from the first reactor is introduced into the second reactor without further purifying it.

    Abstract translation: 本发明涉及一种用于在C4二羧酸和/或其衍生物，包括以下步骤的气相制备任选被烷基取代的1,4-丁二醇，通过两阶段催化氢化：a）将C4二羧酸的气体流或它们的衍生物 在200〜300℃和2至在第一反应器和催化气相加氢在含有产物主要为任选被烷基取代的γ-丁内酯60巴; b）将由此获得进入第二反应器在150℃的温度至240℃的产品流和15至100巴和催化气相任选烷基取代的1,4-丁二醇的压力; c）从中间体，副产物和任选未反应的离析物中分离所需产物; d）任选地回收未转化的中间体在一个或两个氢化阶段，其中，在每种情况下，催化剂在两个氢化中使用的<= 95重量％，优选为5〜95重量％，特别是10至80重量％的CuO 和> = 5具有重量％，优选为5〜95重量％，特别是20至90重量的氧化载体的％，在第二反应器更高的压力占优势比在第一反应器和与第一反应器的产物混合物将取出的 不经进一步纯化而引入第二反应器中。

    3.
    发明专利
    未知

    公开(公告)号：DE50300824D1

    公开(公告)日：2005-08-25

    申请号：DE50300824

    申请日：2003-02-28

    Applicant: BASF AG

    Inventor： WINDECKER GUNTHER ,  WECK ALEXANDER ,  FISCHER ROLF-HARTMUTH ,  ROESCH MARKUS ,  BOTTKE NILS ,  HESSE MICHAEL ,  SCHLITTER STEPHAN ,  BORCHERT HOLGER

    IPC: B01D3/14 ,  C07D307/08

    Abstract: Crude water-containing tetrahydrofuran is purified by passing the crude tetrahydrofuran through three distillation columns, withdrawing water from the bottom of the first column, recycling water-containing tetrahydrofuran from the top of the second column into the first column, passing a sidestream of the first column into the second column, recycling the bottom product of the third column into the first column, and withdrawing a distillate at the top of the first column. Additionally, a sidestream of the second column is passed into the third column and the purified tetrahydrofuran is recovered as the top product of the third column.

    METHOD FOR THE PRODUCTION OF 1,4- BUTANE-DIOL BY COMBINED GAS-PHASE AND LIQUID-PHASE HYDROGENATION
    8.
    发明专利
    METHOD FOR THE PRODUCTION OF 1,4- BUTANE-DIOL BY COMBINED GAS-PHASE AND LIQUID-PHASE HYDROGENATION 未知

    公开(公告)号：AU2003274707A1

    公开(公告)日：2003-12-22

    申请号：AU2003274707

    申请日：2003-06-10

    Applicant: BASF AG

    Inventor： BOTTIKE NILS ,  FISCHER ROLF-HARTMUTH ,  WECK ALEXANDER ,  WINDECKER GUNTHER ,  HEYDRICH GUNNAR ,  HESSE MICHAEL ,  SCHLITTER STEPHAN ,  BORCHERT HOLGER ,  SCHUBERT MARKUS ,  ROSCH MARKUS

    IPC: B01J23/80 ,  C07B61/00 ,  C07C29/149 ,  C07C31/20

    Abstract: The present invention relates to a process for preparing optionally alkyl-substituted 1,4-butanediol by two-stage catalytic hydrogenation in the gas phase of C 4 -dicarboxylic acids and/or of derivatives thereof having the following steps: a) introducing a gas stream of a C 4 -dicarboxylic acid or of a derivative thereof at from 200 to 300° C. and from 2 to 60 bar into a first reactor and catalytically hydrogenating it to a product which contains mainly optionally alkyl-substituted gamma-butyrolactone; b) converting the product stream into the liquid phase; c) introducing the product stream obtained in this way into a second reactor at a temperature of from 100° C. to 240° C. and a pressure of from 20 to 250 bar and catalytically hydrogenating it in the liquid phase to optionally alkyl-substituted 1,4-butanediol; d) removing the desired product from by-products and any unconverted reactants; e) optionally recycling unconverted intermediates into one or both hydrogenation stages, said hydrogenation stages both using a catalyst which comprises =5% by weight, preferably from 5 to 95% by weight, in particular from 20 to 90% by weight, of a support, said second reactor having a higher pressure than said first reactor, and the product mixture removed from said first reactor being introduced without further purification into said second reactor.

    TWO-STAGE METHOD FOR PRODUCING BUTANDIOL IN TWO REACTORS
    9.
    发明专利
    TWO-STAGE METHOD FOR PRODUCING BUTANDIOL IN TWO REACTORS 未知

    公开(公告)号：AU2003238491A1

    公开(公告)日：2003-12-22

    申请号：AU2003238491

    申请日：2003-06-10

    Applicant: BASF AG

    Inventor： HESSE MICHAEL ,  SCHLITTER STEPHAN ,  BORCHERT HOLGER ,  SCHUBERT MARKUS ,  ROSCH MARKUS ,  BOTTKE NILS ,  FISCHER ROLF-HARTMUTH ,  WECK ALEXANDER ,  WINDECKER GUNTHER ,  HEYDRICH GUNNAR

    IPC: C07C29/149 ,  C07D315/00 ,  C07D307/33 ,  C07C31/20

    Abstract: The invention relates to a method for producing optionally akyl-substituted 1,4-butandiol by two-stage catalytic hydration in the gaseous phase of C4 dicarboxylic acids and/or the derivatives thereof with the steps of: a) introducing a gaseous flow of a C4 dicarboxylic acid or a derivative thereof at 200 to 300 °C and 2 to 60 bar in a first reactor and catalytic gas phase hydration to a mainly optionally alkyl-substituted gamma-butyrolactone containing product; b) introducing the product flow so obtained into a second reactor at a temperature of from 150 °C to 240 °C and a pressure of from 15 to 100 bar and catalytic gas phase hydration to optionally alkyl-substituted 1,4-butandiol; c) removing the desired product from the intermediates, byproducts and possibly not reacted educt; d) optionally returning non-reacted intermediates to one or both hydration stages, whereby in both hydration stages one catalyst each is used which comprises = 5 % by weight, preferably 5 to 95 % by weight, especially 20 to 90 % by weight of an oxidic carrier, the pressure prevailing in the second reactor is higher than in the first reactor, and the product mixture removed from the first reactor is introduced into the second reactor without further purifying it.

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