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    Method for producing alkyl aryl sulphonates
    71.
    发明专利
    Method for producing alkyl aryl sulphonates 未知

    公开(公告)号：AU8767801A

    公开(公告)日：2002-02-25

    申请号：AU8767801

    申请日：2001-08-10

    Applicant: BASF AG

    Inventor： MAAS HEIKO ,  NARBESHUBER THOMAS ,  ROPER MICHAEL

    IPC: C07B61/00 ,  C07C15/107 ,  C07C303/06 ,  C07C303/32 ,  C07C309/31 ,  C11D1/22 ,  C11D11/04

    Abstract: The invention relates to a process for the preparation of alkylarylsulfonates by a) reaction of a C 4 -olefin mixture over a metathesis catalyst for the preparation of an olefin mixture comprising 2-pentene and/or 3-hexene, and optional removal of 2-pentene and/or 3-hexene, b) dimerization of the 2-pentene and/or 3-hexene obtained in stage a) over a dimerization catalyst to give a mixture containing C 10-12 -olefins, and optional removal of the C 10-12 -olefins, c) reaction of the C 10-12 -olefin mixtures obtained in stage b) with an aromatic hydrocarbon in the presence of an alkylating catalyst to form alkylaromatic compounds, where, prior to the reaction, additional linear olefins may be added, d) sulfonation of the alkylaromatic compounds obtained in stage c), and neutralization to give alkylarylsulfonates, where, prior to the sulfonation, linear alkylbenzenes may additionally be added, e) optional mixing of the alkylarylsulfonates obtained in stage d) with linear alkylarylsulfonates.

    74.
    发明专利
    未知

    公开(公告)号：ES2151673T3

    公开(公告)日：2001-01-01

    申请号：ES96928377

    申请日：1996-07-26

    Applicant: BASF AG

    Inventor： ACHHAMMER GUNTHER ,  ROPER MICHAEL

    IPC: C07C67/54 ,  C07C69/716

    Abstract: PCT No. PCT/EP96/03290 Sec. 371 Date Jan. 27, 1998 Sec. 102(e) Date Jan. 27, 1998 PCT Filed Jul. 26, 1996 PCT Pub. No. WO97/06126 PCT Pub. Date Feb. 20, 19975-Formylvaleric esters are prepared in a yield of not less than 90% by distillation of a formylvaleric ester mixture of 5-formylvaleric ester and either 3- or 4-formylvaleric ester or a mixture of 3- and 4-formylvaleric esters, where the ester radicals of the respective formylvaleric esters are identical, wherein the 3- or 4-formylvaleric ester or a mixture thereof is separated from the 5-formylvaleric ester in a distillation column at a pressure in the range from 2 to 100 mbar and a temperature of not above 150 DEG C. (measured as the temperature at the bottom of the column) and the esters used are the corresponding methyl or ethyl esters, where the purity of the 5-formylvaleric ester is not less than 98% and, as impurity, 4-formylvaleric ester is present in an amount of not more than 100 ppm.

    77.
    发明专利
    未知

    公开(公告)号：TR199900222T2

    公开(公告)日：2000-09-21

    申请号：TR9900222

    申请日：1997-07-23

    Applicant: BASF AG

    Inventor： FISCHER ROLF ,  PACIELLO ROCCO ,  ROPER MICHAEL ,  SCHNURR WERNER

    IPC: B01J31/18 ,  B01J31/24 ,  C07C209/26 ,  C07C253/30 ,  C07C255/24 ,  C07F9/6574

    Abstract: PCT No. PCT/EP97/03988 Sec. 371 Date Feb. 1, 1999 Sec. 102(e) Date Feb. 1, 1999 PCT Filed Jul. 23, 1997 PCT Pub. No. WO98/05632 PCT Pub. Date Feb. 12, 1998Manufacture of 6-aminocapronitrile or 6-aminocapronitrile/hexamethylene diamine mixtures, involving a) the reaction of at least one pentennitrile, selected from the group consisting of 2,3 and 4-pentennitrile with carbon monoxide and hydrogen in the presence of catalysts, which contain at least one element of the eighth subgroup as active components, obtaining a hydrogenation formylating discharge (I), b) the optional separation of carbon monoxide, hydrogen and the catalyst from the hydrogenation formylating discharge (I), obtaining a hydrogenation formylating discharge (II), c) the separation of 5-formyl valeronitrile from the hydrogenation formylating discharge (I) or (II), d) the reaction of separated 5-formyl valeronitrile with ammonia and hydrogen in the presence of hydrogenating catalysts, selected from the group consisting of rhenium, copper and its compounds as well as metals and metallic compounds of the eighth group, obtaining a hydrogenation discharge, and e) obtaining 6-aminocapronitrile and if necessary hexamethylene diamine.

    PROCESS FOR PREPARING N-BUTYL ALKYL ETHERS
    79.
    发明专利
    PROCESS FOR PREPARING N-BUTYL ALKYL ETHERS 未知

    公开(公告)号：CZ85399A3

    公开(公告)日：1999-12-15

    申请号：CZ85399

    申请日：1997-08-29

    Applicant: BASF AG

    Inventor： KANAND JURGEN ,  ROPER MICHAEL

    IPC: B01J31/24 ,  C07B61/00 ,  C07C41/00 ,  C07C41/06 ,  C07C41/20 ,  C07C41/32 ,  C07C43/00 ,  C07C43/04

    Abstract: In a process for producing n-butylalkyl ethers, (a) 1,3-butadiene or a butadiene-containing hydrocarbon mixture is reacted with an alcohol of formula ROH (I), in which the radical R is a C2-C20 alkyl or alkenyl group substituted or not with 1 to 2 C1-C10 alkoxy or hydroxy groups, a C6-C10 aryl or C7-C11 aralkyl group or a methyl group, at an increased temperature and pressure in the presence of a Brönsted acid or in the presence of a complex of an element of groups Ib, VIIb or VIIIb of the periodic table of elements with a phosphorus- or nitrogen-containing ligand, yielding a mixture of addition products of formulas (II) and (III); (b) the isomers are separated; (c) addition product III is isomerised into addition product II; (d) addition product II is hydrogenated in the presence of a homogeneous or heterogeneous transition metal element catalyst in the liquid phase or in the presence of a heterogeneous, transition metal element-containing catalyst in the gas phase, yielding n-butylalkyl ether of formula (IV).

    PROCESS FOR PREPARING ALKOXYBUTENES
    80.
    发明专利
    PROCESS FOR PREPARING ALKOXYBUTENES 未知

    公开(公告)号：CZ91399A3

    公开(公告)日：1999-06-16

    申请号：CZ91399

    申请日：1997-08-29

    Applicant: BASF AG

    Inventor： KANAND JURGEN ,  ROPER MICHAEL

    IPC: C07C41/00 ,  C07B61/00 ,  C07C41/06 ,  C07C43/00 ,  C07C43/15

    Abstract: In a process for producing alkoxybutenes, 1,3-butadiene or a butadiene-containing hydrocarbon mixture is reacted with an alcohol of formula ROH (I) at an increased temperature and pressure in the presence of a Brönsted acid, yielding a mixture of addition products of formulas (II) and (III), in which the radical R is a C2-C20 alkyl, alkenyl, cycloalkyl or cycloalkenyl group substituted or not with 1 to 2 C1-C10 alkoxy or hydroxy groups, or is a C2-C10 aryl or C7-C11 aralkyl group or a methyl group. The disclosed improvement consists in that the reaction is carried out in the presence of water.

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