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公开(公告)号:MY134006A
公开(公告)日:2007-11-30
申请号:MYPI20010937
申请日:2001-03-01
Applicant: BASF AG
Inventor: DR ROLF PINKOS , DR FRANK STEIN , DR THOMAS N0XD6BEL , DR SYLVIA HUBER-DIRR , DR JOACHIM WULFF-DORING , DR ROLF-HARTMUTH FISCHER , DR STEPHAN ANDREAS SCHUNK
IPC: C07C29/136 , B01J21/18 , B01J23/656 , B01J23/89 , C07C29/14 , C07C29/145 , C07C29/147 , C07C29/17
Abstract: IN A PROCESS FOR PREPARING ALCOHOLS BY CATALYTIC HYDROGENATION OF CARBONYL COMPOUNDS OVER A CATALYST COMPRISING RHENIUM ON ACTIVATED CARBON, THE CATALYST USED COMPRISES RHENIUM (CALCULATED AS METAL) IN A WEIGHT RATIO TO THE ACTIVATED CARBON OF FROM 0.0001 TO 0.5, PLATINUM (CALCULATED AS METAL) IN A WEIGHT RATIO TO THE ACTIVATED CARBON OF FROM 0.0001 TO 0.5 AND, IF APPROPRIATE,AT LEAST ONE FURTHER METAL SELECTED FROM AMONG Zn, Cu, Ag, Au, Ni, Fe, Ru, Mn, Cr, Mo, W AND V IN A WEIGHT RATIO TO THE ACTIVATED CARBON OF FROM 0 TO 0.25, AND THE ACTIVATED CARBON HAS BEEN NONOXIDATIVELY PRETREATED. IT IS ALSO POSSIBLE TO PREPARE ETHERS AND LACTONES IF THE HYDROGEN PRESSURE IS NOT MORE THAN 2500 kPa (25 BAR). IN THIS CASE, THE ACTIVATED CARBON IN THE CATALYST MAY ALSO HAVE BEEN NONOXIDATIVELY PRETREATED.
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公开(公告)号:MY127165A
公开(公告)日:2006-11-30
申请号:MYPI20015603
申请日:2001-12-10
Applicant: BASF AG
Inventor: DR MICHAEL HESSE , DR FRANK STEIN , ALEXANDER WECK , DR RALF-THOMAS RAHN , DR STEPHAN SCHLITTER , DR MARKUS R0XD6SCH , DR BORCHERT HOLGER , DR ROLF-HARTMUTH FISCHER
IPC: C07D307/08 , C07B61/00 , C07C51/36 , C07C55/10 , C07D307/32 , C07D307/33
Abstract: C?-DICARBOXYLIC ACIDS OR DERIVATIVES THEREOF ARE HYDROGENATED IN THE GAS PHASE IN A FLUIDIZED-BED REACTOR. IT IS POSSIBLE TO USE CATALYST COMPOSITIONS KNOWN PER SE.
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3.
公开(公告)号:MY126887A
公开(公告)日:2006-10-31
申请号:MYPI20015305
申请日:2001-11-20
Applicant: BASF AG
Inventor: DR HOLGER BORCHERT , DR FRANK STEIN , DR GERD KAIBEL , ALEXANDER WECK , DR ROLF-HARTMUTH FISCHER , DR RALF-THOMAS RAHN , DR STEPHAN SCHLITTER , DR MARKUS R0XD6SCH
IPC: C07D307/08 , C07B61/00 , C07D307/33
Abstract: THE PRESENT INVENTION RELATES TO A PROCESS FOR THE GAS-PHASE HYDROGENATION OF C?-DICARBOXYLIC ACIDS AND/OR THEIR DERIVATIVES OVER A CATALYST BASED ON COPPER OXIDE TO GIVE SUBSTITUTED OR UNSUBSTITUTED Y-BUTYROLACTONE AND/OR TETRAHYDROFURAN, WHICH A FIRST REACTION ZONE IN WHICH THE C?-DICARBOXYLIC ACID AND /OR ITS DERIVATIVES IS/ARE REACTED TO GIVE A MIXTURE COMPRISING A SUBSTITUTED OR UNSUBSTITUTED TUTED Y-BUTROLACTONE AS MAIN PRODUCT AND A SUBSEQUENT SECOND REACTION ZONE IN WHICH THE SUBSTITUTED OR UNSUBSTITUTED Y-BUTYROLACTONE PRESENT IN THE MIXTURE FROM THE FIRST HYDROGENATION STEP IS REACTED AT A TEMPERATURE LOWER THAN THE TEMPERATURE IN THE FIRST HYDROGENATION STEP TO GIVE SUBSTITUTED OR UNSUBSTITUTED TETRAHYDROFURAN.
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公开(公告)号:MY126723A
公开(公告)日:2006-10-31
申请号:MYPI20002698
申请日:2000-06-14
Applicant: BASF AG
Inventor: HARALD RUST , THOMAS KRUG , DR FRANK STEIN , DR THOMAS N0XD6BEL
Abstract: A PROCESS FOR PREPARING 1,6-HEXANEDIOL FROM A CARBOXYLIC ACID MIXTURE COMPRISING ADIPIC ACID, 6-HIDROXYCAPROIC ACID AND SMALL AMOUNTS OF 1,4- CYCLOHEXANEDIOLS WHICH IS OBTAINED AS BY-PRODUCT IN THE OXIDATION OF CYCLOHEXANE TO CYCLOHEXANONE/CYCLOHEXANOL AFTER WATER EXTRACTION OF THE REACTION MIXTURE FOLLOWED BY EXTRACTION WITH AQUEOUS SODIUM HYDROXIDE SOLUTION, BY ESTERIFICATION OF THE ACIDS AND HYDROGENATION COMPRISES A) LIBERATING THE CARBOXYLIC ACIDS FROM THE ALKALINE EXTRACT BY ADDITION OF A MINERAL ACID,B) FRACTIONATING THE ORGANIC PHASE COMPRISING CARBOXYLIC ACIDS TO GIVE A DISTILLATE COMPRISING THE LOW MOLECULAR WEIGHT MONOCARBOXYLIC ACIDS AND A RESIDUE COMPRISING ADIPIC ACID AND 6-HYDROXYCAPROIC ACID,C) REACTING THE MONOCARBOXYLIC AN DICARBOXYLIC ACIDS PRESENT IN THE AQUEOUS DICARBOXYLIC ACIDS MIXTURE WITH A LOW MOLECULAR WEIGHT ALCOHOL TO GIVE THE CORRESPONDING CARBOXYLIC ESTERS, D) FREEING THE ESTERIFICATION MIXTURE OBTAINED OF EXCESS ALCOHOL AND LOW BOILERS IN A FIRST DISTILLATION STEP,E) FRACTIONATING THE BOTTOM PRODUCT IN A SECOND DISTILLATION STEP TO GIVE AN ESTER FRACTION ESSENTIALLY FREE OF 1,4-CYCLOHEXANEDIOLS AND A FRACTION COMPRISING AT LEAST THE MAJOR PART OF THE 1,4-CYCLOHEXANEDIOLS, F) CATALYTICALLY HYDROGENATING THE ESTER FRACTION WHICH IS ESSENTIALLY FREE OF 1,4-CYCLOHEXANEDIOLS AND G) ISOLATING 1,6-HEXANEDIOL FROM THE HYDROGENATION PRODUCT IN A MANNER KNOWN PER SE IN A FINAL DISTILLATION STEP.FIG.1
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