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公开(公告)号:JP2005132841A
公开(公告)日:2005-05-26
申请号:JP2004312897
申请日:2004-10-27
Applicant: Basf Ag , ビーエーエスエフ アクチェンゲゼルシャフト
Inventor: KESSINGER ROLAND , ARNDT JAN-DIRK , HENKELMANN JOCHEN , THOMAS FLORIAN
CPC classification number: C07F9/4015
Abstract: PROBLEM TO BE SOLVED: To provide a process for preparation of an alkenylphosphonic acid derivative free from formation of a coupling product, accepting reaction temperature below 200°C, accepting high yield more than 75%, being sufficient without use of an expensive noble metal catalyst and having improved yield and selectivity compared to conventional process.
SOLUTION: The invention relates to the process for preparation of the alkenylphosphonic acid derivative by reacting the phosphonic acid derivative in the presence of an alkyne and a complex catalyst system, wherein the complex catalyst system comprise (a) nickel and (b) a phosphine having at least two trivalent phosphorus atoms and/or (c) a phosphine having one trivalent phosphorus atom, in which the addition of the alkyne is carried out after at least one minute of contact of the phosphonic acid derivative with the complex catalyst system.
COPYRIGHT: (C)2005,JPO&NCIPIAbstract translation: 要解决的问题:提供一种制备不形成偶合产物的烯基膦酸衍生物的方法,接受低于200℃的反应温度,接受高产率大于75%,足以不使用昂贵的 贵金属催化剂,并且与常规方法相比具有提高的产率和选择性。 解决方案:本发明涉及通过在炔烃和络合催化剂体系存在下使膦酸衍生物反应来制备烯基膦酸衍生物的方法,其中复合催化剂体系包含(a)镍和(b) 具有至少两个三价磷原子的膦和/或(c)具有一个三价磷原子的膦,其中在将膦酸衍生物与络合催化剂体系接触至少一分钟后进行炔的添加 。 版权所有(C)2005,JPO&NCIPI
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公开(公告)号:JPH11349833A
公开(公告)日:1999-12-21
申请号:JP13436099
申请日:1999-05-14
Applicant: BASF AG
Inventor: BLUM RAINER , KELLER PETER DR , PREISS THOMAS DR , HENKELMANN JOCHEN
Abstract: PROBLEM TO BE SOLVED: To provide a dye useful for dye thermal transfer, dyeing and printing by selecting a specific (aza)methine dye with a 5-membered heterocycle having CF3 group as a central forming block and without a water-soluble group. SOLUTION: A dye represented by the formula: Q -X=Het [wherein X is N or CH; Q is one selected from groups represented by formulas I to V or the like; Het is a divalent group represented by formula VI or VII; n is 0 or 1; Z is H, a 1-13C alkyl, 1-4C alkoxy, OH or the like; Z is the same as Z or a 1-4C alkoxy; Z and Z are each H, a 1-13C alkyl, 3-4C alkenyl or the like; Z is H or a 1-4C alkyl; Z is H, a halogen, 1-13C alkyl or the like; Z is H, a 1-13C alkyl, phenyl or the like; Y is O, S, (1-4C alkyl)imino, phenylimino or a group of an acidic CH compound; A is N or a group represented by the formula: C-U; U is H, a 1-13C alkyl, halogen, CN or 1-13C alkoxycarbonyl; E is O, S, Se, a (1-4C alkyl)imino or phenylimino] is selected. For example, a dye represented by formula VIII is cited.
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公开(公告)号:JPH11322738A
公开(公告)日:1999-11-24
申请号:JP9894599
申请日:1999-04-06
Applicant: BASF AG
Inventor: BRUNNER MELANIE DR , BREITSCHEIDEL BORIS DR , HENKELMANN JOCHEN , BOETTCHER ARND DR
IPC: C07D307/62 , C07C29/141 , C07C29/145 , C07C31/26
Abstract: PROBLEM TO BE SOLVED: To obtain a sugar alcohol useful in a food industry, cosmetics, agents and an industrial field by hydrogenating a saccharide in the presence of a catalyst composed of a transition metal. SOLUTION: A saccharide (preferably glucose, mannose or the like) or a mixture of two or more of saccharides is brought into contact with hydrogen in the presence of a catalyst to give a sugar alcohol or a mixture of two or more of the sugar alcohols. The catalyst comprises at least one homogeneous compound of at least one transition metal of the group VIII of the periodic table or optionally the homogeneous compound and at least one homogeneous compound of at least one transition metal of the group I or group VII of the periodic table and is deposited on a carrier on-site. Preferably 0.01-30 wt.% based on the total weight of the catalyst is supported on a carrier, 5-50% pore volume of the catalyst comprises macropores having 50-10,000 nm pore diameters, 50-95 % pore volume comprises mesopores having 2-50 nm pore diameters and the sum of the pore volume is 100%.
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公开(公告)号:WO8902886A3
公开(公告)日:1989-05-05
申请号:PCT/EP8800854
申请日:1988-09-21
Applicant: BASF AG
Inventor: EGGERSDORFER MANFRED , HENKELMANN JOCHEN , GROSCH WALTER
CPC classification number: C07C46/00 , C01B15/023 , C07C50/18
Abstract: The new 2-neopentylanthraquinone compound, which is produced by Friedel-Crafts acylation of neopenthylbenzene with phthalic anhydride followed by cyclization of the 2-(4-neopentylbenzoyl) benzoic acid obtained in the presence of strong anhydrous acids, is a catalyst for the manufacture of hydrogen peroxide.
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公开(公告)号:FI88914B
公开(公告)日:1993-04-15
申请号:FI872515
申请日:1987-06-04
Applicant: BASF AG
Inventor: EGGERSDORFER MANFRED , SIEGEL HARDO , SCHUHMACHER ALFRED , GROSCH WALTER , HENKELMANN JOCHEN
IPC: C07B41/06 , B01J31/00 , B01J31/12 , B01J31/14 , C07B31/00 , C07B61/00 , C07C45/00 , C07C45/46 , C07C49/76 , C07C51/083 , C07C51/373 , C07C65/34 , C07C67/00
Abstract: 1. A process for the acylation of an aromatic by the Friedel-Crafts method, wherein the acylation is carried out in the presence of a metalalkyl or metalalkyl halide of a metal or semimetal of main groups two to five and/or of a metal of subgroups two or four of the Periodic Table.
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公开(公告)号:BR0108422A
公开(公告)日:2003-03-25
申请号:BR0108422
申请日:2001-02-16
Applicant: BASF AG
Inventor: HENKELMANN JOCHEN , MAAS HEIKO , SCHULZ GERHARD , STAMM ARMIN , RINK HEINZ-PETER , JUNG WERNER-ALFONS , SCHWAB PETER
IPC: C07C263/10 , C07C265/14 , C08G18/62 , C08G18/72 , C08G18/73 , C09D175/04 , C09J175/04
Abstract: A description is given of polyisocyanates of the formula I in which R and R' are identical or different and are alkyl groups having 1-4 carbon atoms and n is on average from 1.5 to 5 and also of a process for preparing these polyisocyanates in which a polyamine of the formula II in which R, R', and n are as defined above, is reacted with phosgene. The new polyisocyanates are suitable for producing crosslinked polyurethanes from reaction mixtures with low solvent content and for producing coating compositions or adhesives. Also described are the coating compositions and adhesives, and their use.
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公开(公告)号:DE102004057146A1
公开(公告)日:2006-06-01
申请号:DE102004057146
申请日:2004-11-26
Applicant: BASF AG
Inventor: ROHDE THORSTEN , HENKELMANN JOCHEN
IPC: C07C51/60 , B01J31/24 , C07C63/331
Abstract: A process for preparing phthaloyl chloride by reacting phthalic anhydride with a chlorinating agent (I) selected from the group of thionyl chloride and phosgene in the presence of a catalyst at a temperature of from 80 to 200° C. and a pressure of from 0.01 to 10 MPa abs, in which the catalyst (II) used is triphenylphosphine, triphenylphosphine oxide or a mixture thereof.
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公开(公告)号:NO872383A
公开(公告)日:1987-12-07
申请号:NO872383
申请日:1987-06-05
Applicant: BASF AG
Inventor: EGGERSDORFER MANFRED , SIEGEL HARDO , SCHUHMACHER ALFRED , GROSCH WALTER , HENKELMANN JOCHEN
IPC: C07B41/06 , B01J31/00 , B01J31/12 , B01J31/14 , C07B31/00 , C07B61/00 , C07C45/00 , C07C45/46 , C07C49/76 , C07C51/083 , C07C51/373 , C07C65/34 , C07C67/00 , C07C
CPC classification number: C07C51/373 , C07C45/46 , C07C49/76 , C07C65/34
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公开(公告)号:FI872515A0
公开(公告)日:1987-06-04
申请号:FI872515
申请日:1987-06-04
Applicant: BASF AG
Inventor: EGGERSDORFER MANFRED , SIEGEL HARDO , SCHUHMACHER ALFRED , GROSCH WALTER , HENKELMANN JOCHEN
IPC: C07B41/06 , B01J31/00 , B01J31/12 , B01J31/14 , C07B31/00 , C07B61/00 , C07C45/00 , C07C45/46 , C07C49/76 , C07C51/083 , C07C51/373 , C07C65/34 , C07C67/00 , C07C
Abstract: 1. A process for the acylation of an aromatic by the Friedel-Crafts method, wherein the acylation is carried out in the presence of a metalalkyl or metalalkyl halide of a metal or semimetal of main groups two to five and/or of a metal of subgroups two or four of the Periodic Table.
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公开(公告)号:DE10007695A1
公开(公告)日:2001-08-23
申请号:DE10007695
申请日:2000-02-19
Applicant: BASF AG
Inventor: GOETZ ROLAND , STAMM ARMIN , GOETZ NORBERT , KEIL MICHAEL , WOLF BERND , STEINMETZ ADRIAN , HENKELMANN JOCHEN
Abstract: Production of o-chloromethylbenzoyl chlorides (I) by reacting benzo-condensed lactones (II) with thionyl chloride is carried out in the presence of catalytic amounts of (a) a catalyst (III) containing boron, selected from boric acid and anhydride, borates, boronic acid and boronic esters, and (b) a quaternary ammonium salt (IV). Production of o-chloromethylbenzoyl chlorides of formula (I) by reacting benzo-condensed lactones of formula (II) with thionyl chloride is carried out in the presence of catalytic amounts of (a) a catalyst (III) containing boron, selected from boric acid and anhydride, borates, boronic acid and boronic esters, and (b) a quaternary ammonium salt (IV). [Image] R 1-R 4H, 1-4C alkyl, halogen or CF 3.
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