Hydroformylation of compounds containing ethylenically unsaturated double bond(s) comprises reacting with carbon monoxide and hydrogen in the presence of hydroformylation catalyst

    公开(公告)号:DE10205702A1

    公开(公告)日:2002-08-29

    申请号:DE10205702

    申请日:2002-02-12

    Applicant: BASF AG

    Abstract: Process for the hydroformylation of compounds containing ethylenically unsaturated double bond are hydroformylated by reacting with carbon monoxide and hydrogen in the presence of hydroformylation catalyst. Process for the hydroformylation of compounds containing ethylenically unsaturated double bond are hydroformylated by reacting with carbon monoxide and hydrogen in the presence of hydroformylation catalyst that comprises at least one complex of a metal transition group VIII with ligand(s) from compounds of formula (I). [Image] A1>O, S, NRc>, SiRd>Re> or CRf>Rg>; Rc>-Rg>H, (cyclo) alkyl, heterocycloalkyl, aryl or hetaryl, where Rf> and Rg> together with carbon atom to which they are bound may form 3-8-membered carbocycle or heterocycle which may additionally be fused with 1, 2 or 3 cycloalkyl, heterocycloalkyl, aryl and/or hetaryl; Y1>, Y2>radicals containing phosphorus atom(s); Ra>, Rb>H, (cyclo)alkyl, heterocycloalkyl, aryl, hetaryl or (CHRi>CH2O)xRh>; Rh>H, (cyclo)alkyl or aryl; Ri>H, Me or Et; x : 1-120; R1>-R6>H, (cyclo)alkyl, heterocycloalkyl, aryl, hetaryl, COORh>, COO-M+>, SO3Rh>, (SO3)->M+>, NE1>E2>, NE1>E2>E3>+>X->, alkylene-NE1>E2>E3>+>X->, ORh>, SRh>, (CHRi>CH2O)xRh>, (CH2N(E1>))xRh>, (CH2CH2N(E1>))xRh>, halo, trifluoromethyl, nitro, acyl or cyano; Rh>, E1>, E1>, E3>H, (cyclo)alkyl) or aryl; Ri>H, Me or Et; M+>cation; X->anion; and R1> and R2> and/or R3> and R4>together with the adjacent carbon atoms of the benzene ring to which they are bound to form a fused ring system comprising 1,2, or 3 rings. Independent claims are included for: (1) a compound of formula (I); and (2) a catalyst comprising complex(es) of a metal transition group VIII with ligand(s) of formula (I).

    73.
    发明专利
    未知

    公开(公告)号:ES2165087T3

    公开(公告)日:2002-03-01

    申请号:ES97941891

    申请日:1997-07-23

    Applicant: BASF AG

    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.

    75.
    发明专利
    未知

    公开(公告)号:DE59704683D1

    公开(公告)日:2001-10-25

    申请号:DE59704683

    申请日:1997-07-23

    Applicant: BASF AG

    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.

    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

    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 5-AMINOCAPRONITRILE OR MIXTURES OF 6-AMINOCAPRONITRILE AND HEXAMETHYLENEDIAMINE

    公开(公告)号:CZ23899A3

    公开(公告)日:1999-04-14

    申请号:CZ23899

    申请日:1997-07-23

    Applicant: BASF AG

    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.

    Method for producing n-butyraldehyde and/or n-butanol

    公开(公告)号:AU6828998A

    公开(公告)日:1998-10-12

    申请号:AU6828998

    申请日:1998-03-06

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP98/01324 Sec. 371 Date Sep. 15, 1999 Sec. 102(e) Date Sep. 15, 1999 PCT Filed Mar. 6, 1998 PCT Pub. No. WO98/41494 PCT Pub. Date Sep. 24, 1998Process for the preparation of n-butyraldehyde and/or n-butanol, wherein a) 1,3-Butadiene or a butadiene-containing hydrocarbon mixture is reacted with an alcohol of the formula IROHI, where R is C2-C20-alkyl or alkenyl which is unsubstituted or substituted by 1 or 2 C1-C10-alkoxy or hydroxyl groups, or is C6-C10-aryl, C7-C11-aralkyl or methyl, at elevated temperatures and superatmospheric pressure in the presence of a Br+E,uml o+EE nsted acid or in the presence of a complex of an element of Group Ia, VIIA or VIIIA of the Periodic Table of Elements with phosphorus- or nitrogen-containing ligands to give a mixture of the adducts of the formulae II and III b) the adduct III is isomerized to the adduct II, c) the adduct II is converted into the acetal of the formula IV d) n-butyraldehyde and/or n-butanol are then produced from this acetal IV by reacting it, in the liquid phase, with hydrogen and water or water in the presence of a homogeneous or heterogeneous transition metal catalyst which differs from dicobaltoctacarbonyl or hydridocobalttetracarbonyl.

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