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公开(公告)号:AT243184T
公开(公告)日:2003-07-15
申请号:AT01109289
申请日:2001-04-17
Applicant: BASF AG
Inventor: EBEL KLAUS DR
IPC: C07C67/333 , C07C45/61 , C07C45/62 , C07C45/66 , C07C45/67 , C07C49/12 , C07C49/385 , C07C49/587 , C07C67/347 , C07C69/716
Abstract: Novel esters of specific formulas are new. Novel esters of formulae (Ia) and (Ib) , their esters, optically active forms, tautomers, racemates, distereomer mixtures or salts are claimed: R = phenyl or 1-6C alkyl or alkoxyalkyl, where the alkoxy is a combination of an alkoxy group with an oxygen atom, e.g. (m)ethoxy, propoxy, butoxy or pentoxy. Independent claims are included for: (1) preparation of these esters and their mixtures by radically reacting an acetate of formula (II) with 1,9-decandiene; (2) preparation of 1,15-hexadecadiones by reacting the ester of (II) with 1,9-decandiene and decarboxylating; (3) preparation of muscones of formula (III) by further reacting this product in the gaseous phase to give muscones, cyclizing in a mixture with unsaturated muscone derivatives and hydrogenating to muscone.
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公开(公告)号:DE19740112A1
公开(公告)日:1999-03-18
申请号:DE19740112
申请日:1997-09-12
Applicant: BASF AG
Inventor: PAPKALLA THOMAS DR , LUX JUERGEN ALFRED DR , EBEL KLAUS DR
Abstract: In the production of polycarboxylic acids (I), crosslinked polysaccharides (II) are used for oxidation with gaseous nitrogen dioxide/dinitrogen tetroxide in a fluidized bed at 30-150 deg C, in which at least some of the hydroxyl groups of (II) are converted to carboxyl groups and then optionally (partly) neutralized.
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公开(公告)号:DE19636768A1
公开(公告)日:1998-03-12
申请号:DE19636768
申请日:1996-09-10
Applicant: BASF AG
Inventor: FLICK KLEMENS DR , FISCHER ROLF DR , EBEL KLAUS DR , SCHNURR WERNER DR , VOIT GUIDO DR
IPC: B01J23/75 , B01J23/74 , B01J23/76 , B01J25/00 , C07B61/00 , C07C253/30 , C07C255/24 , C07C255/25
Abstract: The invention concerns catalysts suitable for preparing aliphatic alpha-, omega-aminonitriles by partial hydrogenation of aliphatic dinitriles, containing: (a) metallic cobalt, a cobalt compound or their mixtures, the metallic cobalt portion being between 20 and 100 wt % relative to (a); (b) between 10 and 70 wt %, relative to (a), of metallic iron, iron oxide, a further iron compound or their mixtures, the iron oxide portion being between 20 and 100 wt % relative to (b); and (c) between 0 and 1 wt %, relative to (a), of a compound based on an alkali metal, alkaline earth metal or zinc.
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104.
公开(公告)号:DE19636767A1
公开(公告)日:1998-03-12
申请号:DE19636767
申请日:1996-09-10
Applicant: BASF AG
Inventor: EBEL KLAUS DR , FISCHER ROLF DR , FLICK KLEMENS DR , MERGER MARTIN DR , VOIT GUIDO DR
IPC: C07C209/48 , C07C211/12 , C07C253/30 , C07C255/24
Abstract: In the production of aliphatic alpha ,w-aminonitriles (I) by catalytic partial hydrogenation of aliphatic alpha ,w-dinitriles (II), the catalyst contains: (a) iron (Fe) and/or Fe compound(s); (b) 0.01-5 wt.%, with respect to (a), of a promoter based on group 2, 3, 4 or 5 elements selected from aluminium, silicon, zirconium, titanium and vanadium; and (c) 0-0.5 wt.%, with respect to (a), of an alkali(ne earth) metal compound. Preferably component (a) is based on Fe oxide(s) and (b) on Al, Si and V. The catalyst is optionally supported. Simultaneous production of ACN and HMD from ADN comprises: (1) catalytic partial hydrogenation of ADN to a mixture containing ACN, HMD and ADN; (2) separation of ACN and HMD from the mixture; (3) adding an acid or acid ion exchanger to the mixture containing ADN especially in an amount of 0.01-10 wt.% with respect to ADN, ADN is then separated. If ADN is separated by distillation, the acid used has a boiling point above that of ADN at the pressure used for distillation and a pKa value \} 10. The purified ADN is then recycled. Hydrogenation may be carried out in a suspension or stationary bed reactor.
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公开(公告)号:ES2111110T3
公开(公告)日:1998-03-01
申请号:ES93114033
申请日:1993-09-02
Applicant: BASF AG
Inventor: TELES JOAQUIM HENRIQUE DR , MELDER JOHANN-PETER DR , GEHRER EUGEN DR , HARDER WOLFGANG DR , EBEL KLAUS DR , GROENING CARSTEN DR
IPC: B01J31/02 , C07B61/00 , C07C45/75 , C07C47/19 , C07C49/17 , C07D249/08 , C07D249/10 , C07D249/12 , C07D249/14 , C07D257/04 , C07D471/04 , C07D487/04
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公开(公告)号:DE59307979D1
公开(公告)日:1998-02-19
申请号:DE59307979
申请日:1993-09-02
Applicant: BASF AG
Inventor: TELES JOAQUIM HENRIQUE DR , MELDER JOHANN-PETER DR , GEHRER EUGEN DR , HARDER WOLFGANG DR , EBEL KLAUS DR , GROENING CARSTEN DR , MEYER REGINA DR
IPC: B01J31/02 , C07B61/00 , C07C45/75 , C07C47/19 , C07C49/17 , C07D249/08 , C07D249/10 , C07D249/12 , C07D249/14 , C07D257/04 , C07D471/04 , C07D487/04
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公开(公告)号:DE19544450A1
公开(公告)日:1997-06-05
申请号:DE19544450
申请日:1995-11-29
Applicant: BASF AG
Inventor: SCHROEDER JUERGEN DR , BOECK STEFAN DR , EBEL KLAUS DR
IPC: B01J21/04 , B01J21/06 , B01J21/08 , C07B61/00 , C07C41/28 , C07C43/16 , C07C43/166 , C07C43/176 , C07C67/327 , C07C69/734 , C07C69/708 , C07C67/317 , C07C255/15
Abstract: The preparation of enol-ethers of formula R3R4C=C(OR1)R2 is by gas phase reaction at 100-550 (especially 200-350) degrees C and 0.001-5 bar of acetals or ketals of formula R3R4HC-C(OR1)(OR1')R2 on a heterogeneous highly porous catalyst which is an oxide of a Gp. II, III or IV or sub-Gp. II or IV element, the catalyst having a pH of 7-14, a porosity of 40-80% and a BET surface area of 0.5-250 m /g. R1-5 = 1-20 C alkyl, 2-20 C alkenyl or 7-20 C phenylalkyl; R2-4 = H, aryl, CN, COOR5, 1-12 C alkyl (optionally 1-3 times substituted or interrupted by COOR5, CO, CN or 1-12 C alkoxy), aryl or 7-12 C phenylalkyl (each optionally 1-3 times substituted by 1-12 C alkyl, 1-12 C alkoxy, halogen or CN); R2/R4 or R3/R4 = together 3-10 C alkylene or 2-20 C alkylidene; and R1' = R1, but not necessarily the same.
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公开(公告)号:DE59304854D1
公开(公告)日:1997-02-06
申请号:DE59304854
申请日:1993-04-23
Applicant: BASF AG
Inventor: GEHRER EUGEN DR , HARDER WOLFGANG DR , VOGEL HERBERT DR , KNUTH BERNHARD DR , EBEL KLAUS DR , GROENING CARSTEN DR
Abstract: Process for the preparation of dihydroxyacetone by the thiazolium ylide-catalysed condensation of formaldehyde, in which the reaction is carried out in a reaction system consisting of an aqueous phase and at least one organic liquid phase.
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公开(公告)号:DE4435176A1
公开(公告)日:1996-04-04
申请号:DE4435176
申请日:1994-09-30
Applicant: BASF AG
Inventor: GROENING CARSTEN DR , EBEL KLAUS DR , KAIBEL GERD DR , THERRE JOERG DR , KOOPMANN JUERGEN DR , MENIG HELMUTH DR , FRITZ GERHARD DR , DIETZ RAINER
Abstract: Prepn. of methyl glyoxal dimethyl acetal comprises reacting methyl glyoxal and methanol in the presence of a catalyst, in which the acetal is recovered by heating in the presence of water to bring about azeotropic distillation.
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公开(公告)号:ES2082034T3
公开(公告)日:1996-03-16
申请号:ES91107246
申请日:1991-05-04
Applicant: BASF AG
Inventor: EBEL KLAUS DR
IPC: C07D233/54 , C07D233/58 , C07D233/64 , C07D233/68 , C07D521/00
Abstract: Process for the preparation of N-substituted imidazoles of the general formula I … … in which the substituents …… R denotes C1- to C20-alkyl, C2- to C20-alkenyl, C2- to C20-alkynyl, C2- to C20-alkoxyalkyl, C3- to C20-alkenyloxyalkyl, C3- to C12-cycloalkyl, C4- to C20-cycloalkylalkyl, aryl which is unsubstituted or substituted by C1- to C8-alkyl, C1- to C8-alkoxy, halogen, C1- to C4-haloalkyl, C1- to C4-haloalkoxy or phenoxy or denotes C7- to C20-arylalkyl, … the substituents R , R , R , independently of one another, denote hydrogen, C1- to C20-alkyl, C2- to C20-alkoxyalkyl, C3- to C12-cycloalkyl, halogen, aryl which is unsubstituted or substituted by C1- to C8-alkyl, C1- to C8-alkoxy, halogen, C1- to C4-haloalkyl, C1- to C4-haloalkoxy or phenoxy or denote C7- to C20-arylalkyl or R and R together denote a (CH2)n or (CH=CH)m group which is unsubstituted or mono- or disubstituted by C1- to C8-alkyl, C1- to C8-alkoxy and/or halogen and in which n represents 1 to 6 and m represents 1 to 3, … by reaction of imidazoles of the general formula II … … in which R , R and R have the abovementioned meanings, with halides of the general formula III… R -X (III> in which X represents chlorine, bromine or iodine and R has the abovementioned meanings, in aqueous hydroxide solutions at temperatures of 0 to 100 DEG C by carrying out the reaction in the presence of 0.1 to 50 mol % of an N-substituted imidazole, relative to II.
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