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公开(公告)号:DE2414253A1
公开(公告)日:1975-10-16
申请号:DE2414253
申请日:1974-03-25
Applicant: BASF AG
Inventor: KUMMER RUDOLF DIPL CHEM DR
IPC: C07C29/136 , B01J31/00 , C07B61/00 , C07C27/00 , C07C29/141 , C07C29/16 , C07C31/20 , C07C41/50 , C07C67/00
Abstract: 1,6-Hexanediol is manufactured by hydroformylation of 1,3-butadiene by a process wherein an acetal of pent-3-en-1-al is formed in a first hydroformylation step in the presence of lower alkanols or alkanediols and of rhodium catalysts, and is then converted into 1,6-hexanediol in a second hydroformylation step in the presence of cobalt catalysts, followed by hydrogenation.
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公开(公告)号:DE2411440A1
公开(公告)日:1975-09-25
申请号:DE2411440
申请日:1974-03-11
Applicant: BASF AG
IPC: C07C69/02 , B01J21/00 , C07B61/00 , C07C51/00 , C07C51/14 , C07C51/377 , C07C57/065 , C07C67/00 , C07D307/33 , C07D315/00 , C07C57/04 , C07D307/32
Abstract: Methacrylic acid and butyrolactone are manufactured by hydroformylation of allyl esters of lower carboxylic acids in the presence of rhodium catalysts and inert organic solvents, followed by oxidation of the resulting formyl compounds with molecular oxygen (e.g. with air) in the presence of lower fatty acids, without prior removal of the rhodium catalysts, and elimination of the carboxylic acid from the acyloxybutyric acids formed, at from 150 DEG to 500 DEG C, using catalysts such as aluminum oxide, silicates or active charcoal.
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公开(公告)号:DE2401553A1
公开(公告)日:1975-07-17
申请号:DE2401553
申请日:1974-01-14
Applicant: BASF AG
Inventor: KUMMER RUDOLF DIPL CHEM DR
IPC: C07C29/132 , B01J31/00 , C07B61/00 , C07C27/00 , C07C29/141 , C07C29/16 , C07C31/20 , C07C67/00 , B01J31/24
Abstract: The manufacture of 1,4-butanediol by hydroformylation of cyclic acetals of acrolein in the presence of phosphine-modified cobalt carbonyl complexes or rhodium carbonyl complexes and hydrogenation of the 3-formylpropionaldehyde-acetals which are the principal products first formed.
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公开(公告)号:DE3046355A1
公开(公告)日:1982-07-15
申请号:DE3046355
申请日:1980-12-09
Applicant: BASF AG
IPC: C07C27/22 , B01J31/00 , B01J31/24 , B01J31/28 , C07B61/00 , C07C27/00 , C07C29/158 , C07C29/16 , C07C45/49 , C07C45/50 , C07C67/00 , C07C47/02
Abstract: A process for hydroformylating olefinically unsaturated compounds by means of rhodium/triphenylphosphine/carbonyl complexes formed in situ from rhodium acetate, triphenylphosphine and carbon monoxide, wherein the hydroformylation reaction is preceded by a starting phase in which the mixture of the hydroformylation medium, the triphenylphosphine and rhodium acetate is heated at from 90 DEG to 120 DEG C. under a CO/H2 pressure of from 5 to 20 bar and the acetic acid liberated is discharged from the reactor in gaseous form in a stream of CO and H2, until virtually no more acetic acid can be detected in this gaseous discharge.
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公开(公告)号:DE3102281A1
公开(公告)日:1982-01-07
申请号:DE3102281
申请日:1981-01-24
Applicant: BASF AG
Inventor: HOHENSCHUTZ HEINZ DIPL CHEM DR , STROHMEYER MAX DIPL CHEM DR , ELLIEHAUSEN HEINRICH DIPL CHEM , FISCHER KARL DIPL CHEM DR , KUMMER RUDOLF DIPL CHEM DR , HERR MANFRED DIPL ING , REUTEMANN WERNER ING GRAD
Abstract: Hydroformylation of propylene with simultaneous operation by the high-pressure process using cobalt catalysts and the low-pressure process using rhodium catalysts, by employing the waste gas, which still contains considerable amounts of unreacted propylene, CO and H2, obtained from the high pressure plant after the removal of cobalt from the reaction mixture, again in the low-pressure plant.
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公开(公告)号:DE2927734A1
公开(公告)日:1981-02-05
申请号:DE2927734
申请日:1979-07-10
Applicant: BASF AG
Abstract: In the removal and opt. recovery of O2 from gas by treatment with phosphine complexes with Mn (II) halides, the gas, if moist, is predried. Drying prevents an irreversible change, so that the complex retains a large fraction of its activity and can be used for continuous exchange. The complexes are useful for sepg. O2 from air in confined spaces, e.g. ships and aircraft, for removing traces of O2 from gases and esp. as detectors for the O2 content of gases, since they are intensely coloured when combined with O2 and colourless to pale yellow when free from O2. In an example, air was passed into 10 g 9 wt.% soln. of the dimethylphenylphosphine-Mn (II) bromide complex in THF at 20 deg.C and normal pressure. The soln. was yellowish initially and became intensely coloured very rapidly. If 2 ml water were added, the colour disappeared immediately and the O2 binding complex was destroyed. If O2 was introduced again, it was no longer bound. If 60 ml BuOH were added, the complex was destroyed within 15 min.
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公开(公告)号:DE2840168A1
公开(公告)日:1980-03-27
申请号:DE2840168
申请日:1978-09-15
Applicant: BASF AG
Abstract: Aldehydes are prepared by hydroformylating the corresponding olefinically unsaturated compounds with the aid of rhodium-carbonyl complexes which contain tertiary phosphines as ligands, by carrying out the reaction in the presence of compounds of copper, silver or zinc which are soluble in the reaction mixture and do not contain any component which deactivates the rhodium-carbonyl complexes.
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公开(公告)号:DE2837815A1
公开(公告)日:1980-03-13
申请号:DE2837815
申请日:1978-08-30
Applicant: BASF AG
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公开(公告)号:DE2646955A1
公开(公告)日:1978-04-20
申请号:DE2646955
申请日:1976-10-18
Applicant: BASF AG
Abstract: Dimethyl adipate, (I) dimethyl alpha-Me glutarate, (II), and dimethyl Et succinate, (III) are recovered from reaction mixts. prepd. by reacting Me pent-3-enoate with CO, under increased temp. and pressure, in the presence of Co carbonyl, heterocyclic aromatic tert. N bases and MeOH. The reaction mixt. is extd. with paraffinic hydrocarbons having b.pt. 40-120 degrees C in the presence of 0.1-5 wt.% water, w.r.t. reaction mixt. The catalyst-contg. MeOH phase is separated. (I), (II), and (III) are obtd. from paraffinic hydrocarbon phase by distn., e.g. by fractional distn. or several consecutive distns. (I), (II) and (III) mixts. with water glass can be used as oil reinforcing agents. (I) is easily converted to adiponitrile, which can be hydrogenated to hexamethylene diamine, a starting material for high polymers. (I) (II) and (III) are obtd. in pure form and the catalyst is not decomposed and can be recovered in active form. The catalyst-contg. aq. MeOH phase can be re-used for methoxy-carbonylation of Me pent-3-enoate. The recovered paraffinic hydrocarbons can be re-used for extn.
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公开(公告)号:DE2628987A1
公开(公告)日:1978-01-12
申请号:DE2628987
申请日:1976-06-28
Applicant: BASF AG
Inventor: ELLIEHAUSEN HEINRICH DIPL CHEM , HOHENSCHUTZ HEINZ DIPL CHEM DR , STROHMEYER MAX DIPL CHEM DR , KUMMER RUDOLF DIPL CHEM DR
IPC: C07C29/14 , B01J23/00 , B01J23/889 , C07B61/00 , C07C27/00 , C07C29/141 , C07C31/02 , C07C67/00 , C09J123/08 , C09J177/00
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