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公开(公告)号:ES2176855T3
公开(公告)日:2002-12-01
申请号:ES98109834
申请日:1998-05-29
Applicant: BASF AG , MAX PLANCK GESELLSCHAFT
Inventor: STURMER RAINER DR , BORNER ARMIN DR , HOLZ JENS DR , VOSS GUDRUN
Abstract: Phospholane and diphospholane compounds of formula (I) are new. R , R = independently 1-6C alkyl, aryl or alkylaryl (R may also be H); Either A has the same meanings as R , or is a group of formula (i), where B is a 1-5C bridging group. Also claimed are metal complexes of (I) whose metal atom is selected from Rh, Ru, Ir, Pd, Pt or Ni. Also claimed is a method for asymmetric hydrogenation of a starting compound, which comprises reacting it with hydrogen in the presence of the metal complex at 1 - 2 bar.
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公开(公告)号:ES2182451T3
公开(公告)日:2003-03-01
申请号:ES99124191
申请日:1999-12-03
Applicant: BASF AG
Inventor: STURMER RAINER DR , BALDENIUS KAI-UWE DR
IPC: B65D33/28 , C07D309/30 , C07D311/66 , C07D311/70 , C07D407/04 , C07D311/74
Abstract: Preparation of substituted chroman derivatives in multi-stage process from acrolein-aldehyde starting material via new intermediates. Preparation of substituted chroman derivatives of formula (VII) comprises: (a) reacting an acrolein-aldehyde of formula (I) with an acrylonitrile-, acrolein-, acrolein-acetal-, allyl-alcohol- or allyl ether of formula (II) to give the corresponding 3,4-dihydro-2H-pyran of formula (III); (b) treating (III) with an acid to give the corresponding 5-oxo derivative of formula (IV); (c) reacting this with a substituted vinyl-ketone of formula (V) to give a chromen-6-one of formula (VI); and (d) dehydrating to give (VII). X = CN, COOR3, CHO, CH2OR7 or CH(OR8)2; R1 = 1-4C alkyl, 6-18C aryl, 7-18C aralkyl, optionally halogenated 1-4C acyl or an acid labile hydroxy protecting group; R2 = 1-23C alkyl, 2-23C alkenyl, 6-18C aryl or 7-18C aralkyl; R3 = H, 1-4C alkyl, 1-4C haloalkyl, 1-4C hydroxyalkyl or 1-4C aminoalkyl; R4-R6 = H or 1-4C alkyl; R7 = H or 1-4C alkyl; R8 = 1-4C alkyl; or R8+R8 = 2-6C alkenyl optionally branched and optionally substituted by 1-2 carboxyl, cyclohexyl or phenyl. Independent claims are included for: (1) pyran derivatives (III) as new; (2) preparation of (III) using step (a) as above; (3) tetrahydropyran derivatives (IV); (4) preparation of (IV) using steps (a) and (b) as above; (5) chromen-6-one derivatives (VI); (6) preparation of (VI) using step (c) as above.
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公开(公告)号:ES2237523T3
公开(公告)日:2005-08-01
申请号:ES01128602
申请日:2001-11-30
Applicant: BASF AG
Inventor: FUNKE FRANK DR , LIANG SHELUE DR , KRAMER ANDREAS DR , STURMER RAINER DR , HOHN ARTHUR DR
IPC: C07B55/00 , C07B61/00 , C07C209/68 , C07C209/88 , C07C211/03 , C07C209/00 , C07C213/00 , C07C213/02 , C07C217/08
Abstract: Procedimiento para el racemizado de aminas con actividad óptica de la fórmula I en la que R1 y R2 son diferentes, y R1, R2, R3 que significan restos alquilo, cicloalquilo, arilalquilo, arilo, heteroarilo, y restos heterocíclicos, y R3 representa adicionalmente hidrógeno (H), pudiendo portar los restos substituyentes seleccionados a partir del grupo alquilo, cicloalquilo, alcoxi, ariloxi, amino, alquilamino y dialquilamino, mediante reacción de la amina con actividad óptica en presencia de hidrógeno y un catalizador de hidrogenado o deshidrogenado a temperatura elevada, caracterizado porque el catalizador contiene los componentes activos cobre y óxido de cinc y un material soporte.
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公开(公告)号:ES2215533T3
公开(公告)日:2004-10-16
申请号:ES00120644
申请日:2000-09-21
Applicant: BASF AG
Inventor: SCHEIN KARIN DR , BALDENIUS KAI-UWE DR , SIEGEL WOLFGANG DR , STURMER RAINER DR , RUFF DETLEF DR , JAEDICKE HAGEN DR
IPC: C07B61/00 , C07C45/46 , C07C49/825 , C07C67/42 , C07C69/017 , C07C69/16
Abstract: Preparation of monoacetylated hydroquinone compound comprises reacting a dicetylphenol compound with peroxo compounds optionally using an acid in one reaction step. Preparation of monoacetylated hydroquinone compound of formula (I) comprises reacting a dicetylphenol compound of formula (II) with peroxo compounds optionally using an acid. R1-R3 = H or Me. Independent claims are included for: (1) preparation of (II) by reacting phenol compounds of formula (III) with an acetylation agent using an acid catalyst; (2) preparation of monoacetylated hydroquinone compounds (I) by reacting (III) with an acetylation agent using an acid catalyst to give (II) and further reacting with peroxo compounds, optionally in the presence of an acid; and (3) compounds of formula (Ia)-(Ie).
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