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公开(公告)号:DE2519036A1
公开(公告)日:1976-11-11
申请号:DE2519036
申请日:1975-04-29
Applicant: HOECHST AG
Inventor: HILLE ERNST DR , RUECK RUDOLF DR
IPC: C07C231/00 , C07C20060101 , C07C67/00 , C07C231/04 , C07C231/14 , C07C233/78 , C07C103/375 , C07C103/34
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公开(公告)号:CH608786A5
公开(公告)日:1979-01-31
申请号:CH515576
申请日:1976-04-23
Applicant: HOECHST AG
Inventor: HILLE ERNST DR , RUECK RUDOLF DR
IPC: C07C231/00 , C07C20060101 , C07C67/00 , C07C231/04 , C07C231/14 , C07C233/78 , C07C103/375 , C07C103/34
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公开(公告)号:DE2240849A1
公开(公告)日:1974-03-14
申请号:DE2240849
申请日:1972-08-19
Applicant: HOECHST AG
Inventor: KUEMMERLE KURT DR , ALBERS ARNOLD DR , HILLE ERNST DR , HEISE HARTMUT DR
Abstract: Title cpds are prepared by hydrogenating the corresp. nitrobenzenes in aq. phase, using Ni catalysts, and adjusting the pH to 6-7.5 by addn. of oxyacids of 3-or 5-valent P, or of B, CO2 or low-mol. carboxylic acids and strong bases, or the corresp. salts; the additives are metered in such a way that the pH does not fall below the above limit. Nitrobenzenes carrying the above substits. cannot be hydrogenated by previous methods. Only 0.01-10 wt. % Ni catalyst is needed. Lower temps., e.g. 20-120 degrees C, can be used. Aminoacids have esp. strong stabilising effect on the pH.
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公开(公告)号:CH626326A5
公开(公告)日:1981-11-13
申请号:CH281777
申请日:1977-03-07
Applicant: HOECHST AG
Inventor: KUEMMERLE KURT DR , HEISE HARTMUT DR , HILLE ERNST DR
IPC: C07B61/00 , B01J23/00 , B01J23/40 , B01J23/74 , B01J31/00 , B01J31/02 , C07C20060101 , C07C67/00 , C07C231/00 , C07C231/12 , C07C235/16 , C07C235/24 , C07C103/34
Abstract: The liquid-phase catalytic hydrogenation of N-acetoacetyl arylamides to yield 3-hydroxybutyric acid arylamides proceeds much faster when amines, phosphines or trialkylphosphates are added. Thus, even with lower hydrogen pressures and at lower temperatures with a lower catalyst concentration, shorter reaction times are sufficient.
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公开(公告)号:CH603597A5
公开(公告)日:1978-08-31
申请号:CH515476
申请日:1976-04-23
Applicant: HOECHST AG
Inventor: SAHM WILFRIED DR , HILLE ERNST DR , SCHILLER WOLFGANG
IPC: C07D235/26
Abstract: 5-Acetoacetylamino benzimidazolone-(2) is obtained in high yield and excellent purity by reacting diketene with the aqueous solution of a salt of 5-amino-benzimidazolone-(2) and an acid having a pKa value of 1 to 7, preferably in the presence of an antioxidant and/or a reducing agent.
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公开(公告)号:CH594600A5
公开(公告)日:1978-01-13
申请号:CH1513475
申请日:1975-11-21
Applicant: HOECHST AG
Inventor: PASZTHORY EMMERICH DR , MEES BERNHARD DR , HILLE ERNST DR
IPC: C07B61/00 , C07C20060101 , C07C67/00 , C07C213/00 , C07C213/02 , C07C217/84 , C07C93/14
Abstract: 1527892 Preparation of 4-chloro-2,5-dimethoxyaniline HOECHST AG 25 Nov 1975 [25 Nov 1974] 48445/75 Heading C2C 4 - Chloro - 2,5 - dimethoxyaniline or a salt thereof is obtained by treating a mixture comprising water and particles of 4-chloro-2,5- dimethoxynitrobenzene having an average size of less than 100 microns with hydrogen in the presence of a nickel catalyst, and if desired, converting the 4-chloro-2,5-dimethoxyaniline to a salt thereof.
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公开(公告)号:DE2609835A1
公开(公告)日:1977-09-22
申请号:DE2609835
申请日:1976-03-10
Applicant: HOECHST AG
Inventor: KUEMMERLE KURT DR , HEISE HARTMUT DR , HILLE ERNST DR
IPC: C07B61/00 , B01J23/00 , B01J23/40 , B01J23/74 , B01J31/00 , B01J31/02 , C07C20060101 , C07C67/00 , C07C231/00 , C07C231/12 , C07C235/16 , C07C235/24 , C07C103/34
Abstract: The liquid-phase catalytic hydrogenation of N-acetoacetyl arylamides to yield 3-hydroxybutyric acid arylamides proceeds much faster when amines, phosphines or trialkylphosphates are added. Thus, even with lower hydrogen pressures and at lower temperatures with a lower catalyst concentration, shorter reaction times are sufficient.
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公开(公告)号:DE2518984B1
公开(公告)日:1976-10-21
申请号:DE2518984
申请日:1975-04-29
Applicant: HOECHST AG
Inventor: PASZTHORY EMMERICH DR , HILLE ERNST DR , SEIFERT KARL-GERHARD DR , ZIMMERMANN VINCENZ
IPC: C07C235/80 , C07C67/00 , C07C231/00 , C07C231/04 , C07C233/16 , C07C103/38
Abstract: N-acetoacetyl-2,5-dimethoxy-4-chloroanilide is obtained in high yield and purity by suspending 2,5-dimethoxy-4-chloroaniline in water and adding the complete amount of diketene necessary altogether at the beginning of the reaction. The product is obtained in a purity allowing its use as an azoic coupling component without purification.
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