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公开(公告)号:DE2910132A1
公开(公告)日:1980-09-25
申请号:DE2910132
申请日:1979-03-15
Applicant: BASF AG
IPC: B01J23/38 , C07C271/06 , C07C125/06
Abstract: Prepn. of aromatic urethanes (I) by catalytic reaction of an aromatic amine with a hydroxyl cpd., CO and an oxidising agent, either oxygen or a nitro cpd., is carried out at >=100 degrees C and >=50 bar in the presence of either (a) a noble metal and/or its oxide, sulphate, nitrate, halide and/or acetate as catalyst; or (b) catalytic amts. of Se and/or S contg. catalysts with additional basic cpds. as auxiliary catalysts. (I) are starting materials in prepn. of dyes, plant protecting agents, pharmaceuticals and polyurethanes. (I) can be used in prepn. of corresp. isocyanates and ureas (intermediates for above prods.). Process gives (I) in better yields, space-time yields and purity than previous processes which gave yields of e.g. 30%.
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公开(公告)号:DE2713195A1
公开(公告)日:1978-10-05
申请号:DE2713195
申请日:1977-03-25
Applicant: BASF AG
Inventor: KUMMER RUDOLF DIPL CHEM DR , SCHNEIDER HEINZ-WALTER DIPL CH , PLATZ ROLF DIPL CHEM DR , MAGNUSSEN PETER DIPL CHEM DR , WEISS FRANZ-JOSEF DIPL CHEM DR
Abstract: A process for the manufacture of butanedicarboxylic acid esters, wherein (A) AN AQUEOUS COBALT SALT SOLUTION IS TREATED, AT FROM 50 DEG TO 200 DEG C. and under a pressure of from 50 to 500 bars, with excess carbon monoxide and hydrogen in the presence of active charcoal laden with cobalt carbonyl, (B) THE RESULTING AQUEOUS SOLUTION OF COBALT CARBONYL HYDRIDE IS EXTRACTED WITH BUTADIENE OR WITH A HYDROCARBON MIXTURE CONTAINING BUTADIENE AND THE AQUEOUS PHASE IS SEPARATED OFF, (C) THE BUTADIENE, OR BUTADIENE-HYDROCARBON MIXTURE, CONTAINING COBALT CARBONYL HYDRIDE, COBALT CARBONYL AND BUTENYL-COBALT TRICARBONYL IS REACTED WITH CARBON MONOXIDE AND AN EXCESS OF AN ALKANOL OF 1 TO 4 CARBON ATOMS IN THE PRESENCE OF FROM 0.5 TO 2 MOLES, PER MOLE OF BUTADIENE, OF A TERTIARY NITROGEN BASE HAVING A PKa of from 3 to 11, at from 80 DEG to 150 DEG C. under a pressure of from 300 to 2,000 bars, and (D) THE RESULTING REACTION MIXTURE IS FREED FROM THE TERTIARY NITROGEN BASE CONTAINED THEREIN, EXCEPT FOR FROM 0.1 TO 0.3 MOLE PER MOLE OF PENTENOIC ACID ESTER, AND FROM EXCESS HYDROCARBONS, THE PENTENOIC ACID ESTER REMAINING IN THE REACTION MIXTURE IS REACTED WITH CARBON MONOXIDE AND AN EXCESS OF AN ALKANOL OF 1 TO 4 CARBON ATOMS AT FROM 140 DEG TO 200 DEG C. and under pressures of from 100 to 400 bars in the presence of the amounts of cobalt carbonyl and tertiary nitrogen base contained in the reaction mixture, and excess alkanol and free nitrogen base are then distilled off, and (E) THE REACTION MIXTURE WHICH REMAINS, AND WHICH CONTAINS COBALT CATALYST, THE BUTANEDICARBOXYLIC ACID ESTER AND BY-PRODUCTS IS TREATED WITH AN OXIDIZING AGENT IN AN AQUEOUS ACID MEDIUM AND THE MIXTURE IS SEPARATED INTO AN ORGANIC PHASE, FROM WHICH THE BUTANEDICARBOXYLIC ACID ESTER IS ISOLATED BY DISTILLATION, AND INTO AN AQUEOUS PHASE CONTAINING COBALT SALTS.
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公开(公告)号:DE2615887A1
公开(公告)日:1977-10-20
申请号:DE2615887
申请日:1976-04-10
Applicant: BASF AG
Inventor: FOUQUET GERD DIPL CHEM DR , MERGER FRANZ DIPL CHEM DR , PLATZ ROLF DIPL CHEM DR , BAER KARL DIPL CHEM DR
IPC: C07C51/353 , C07C69/54 , C07C51/00 , C07C57/04 , C07C67/24
Abstract: Methacrylic acid and methyl methacrylate CH2 = C(CH3)-COOR' (where R1 is H or Me) are made by reacting propionic acid or methyl propionate CH3-CH2-COOR' with formaldehyde dimethylacetal CH3-O-CH2-O-CH3 (I) for 0.1-100 seconds. Reactions is in the presence of (i) 0-0.5 moles water per mol (I) and (ii) a catalyst comprising phosphates and/or silicates of Mg, Ca, Al, Zr, Th or Ti, opt. with the addn. of oxides of Zr, Al, Th and/or Ti and/or boric acid and/or urea. Catalyst is opt. modified by alkali(ne earth) carboxylates or cpds. forming these under the prevailing conditions, pref. with alkali propionate, KOH or LiOH. Process proceeds with high space-time yield and high selectivity to the prodn. of the desired prod. No additional diluent is required and the post treatment for recovery of the prod. is simple and economical in expenditure of energy. The unconverted (I) is easily recycled to the reaction.
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公开(公告)号:DE2435821A1
公开(公告)日:1976-02-12
申请号:DE2435821
申请日:1974-07-25
Applicant: BASF AG
IPC: C07D301/32
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公开(公告)号:DE3205946A1
公开(公告)日:1983-09-01
申请号:DE3205946
申请日:1982-02-19
Applicant: BASF AG
IPC: B01J23/86 , C07C233/00 , C07C103/133 , C07C102/10
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公开(公告)号:DE3031324A1
公开(公告)日:1982-09-30
申请号:DE3031324
申请日:1980-08-20
Applicant: BASF AG
Inventor: RIEBER NORBERT DIPL CHEM DR , BOEHM HEINRICH DIPL CHEM DR , PLATZ ROLF DIPL CHEM DR , FUCHS WERNER DIPL CHEM DR
IPC: C07D261/20
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公开(公告)号:DE2751336A1
公开(公告)日:1979-05-23
申请号:DE2751336
申请日:1977-11-17
Applicant: BASF AG
Inventor: PLATZ ROLF DIPL CHEM DR , DOCKNER TONI DIPL CHEM DR , HENERS JUERGEN DIPL CHEM DR , KRUG HERBERT
IPC: C07B61/00 , B01J23/00 , B01J23/72 , C07C67/00 , C07C231/00 , C07C231/06 , C07C231/08 , C07C233/09 , C07C103/133 , C07C102/08
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公开(公告)号:DE2742034A1
公开(公告)日:1979-03-29
申请号:DE2742034
申请日:1977-09-19
Applicant: BASF AG
Inventor: PLATZ ROLF DIPL CHEM DR , FUCHS WERNER DIPL CHEM DR , RIEBER NORBERT DIPL CHEM DR , JUNG JOHANN , WUERZER BRUNO
IPC: A01N43/02 , A01N43/44 , A01N43/48 , A01N43/62 , A01N43/78 , A01N43/80 , A01N43/90 , A01N57/08 , A01N57/28 , A01N57/30 , A01P21/00 , C07D203/00 , C07D205/00 , C07D205/12 , C07D229/00 , C07D231/00 , C07D231/54 , C07D249/00 , C07D261/00 , C07D303/00 , C07D417/12 , C07D487/08 , C07D487/10 , C07D491/08 , C07D495/04 , C07D495/08 , C07D498/08 , C07D519/00 , A01N5/00 , A01N9/22
Abstract: Tricyclic nitrogenous compounds having strong plant growth regulating properties are disclosed. The compounds display the general formula wherein A is one of several nitrogen-containing radicals, R1, R2, R3 and R4 are selected from various recited aliphatic, aryl, araliphatic and heterocyclic groups. R3 and R4 may also together form one of a number of nitrogen, sulfur and oxygen containing radicals. These compounds have a variety of uses, including the reduction of plant growth height without harm to the plant.
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公开(公告)号:DE2630086A1
公开(公告)日:1978-01-12
申请号:DE2630086
申请日:1976-07-03
Applicant: BASF AG
Inventor: PLATZ ROLF DIPL CHEM DR , KUMMER RUDOLF DIPL CHEM DR , SCHNEIDER HEINZ-WALTER DIPL CH , SCHWIRTEN KURT DIPL CHEM DR
IPC: C07C69/533 , B01J31/00 , C07B61/00 , C07C51/00 , C07C51/14 , C07C57/03 , C07C67/00 , C07C69/52 , C07C57/02 , C07C67/38
Abstract: A process for the manufacture of pent-3-enoic acid and its alkyl esters, of the general formula CH3-CH=CH-CH2-CO-OR where R is hydrogen or alkyl of 1 to 4 carbon atoms, comprising carbonylating butadiene with carbon monoxide and a compound ROH at from 300 to 1,000 bars CO pressure and from 100 DEG to 160 DEG C. in the presence of cobalt catalysts and nitrogen bases, wherein C4 cuts are used as starting materials and a tertiary amine having a pKA of from 3 to 11 is used as the nitrogen base. The pent-3-enoic acid or alkyl esters produced may be used for the manufacture of adipic acid or its alkyl esters, which compounds are starting materials for the manufacture of nylons.
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