PROCESS FOR PREPARING 3-SUBSTITUTED 2-ALKENALS, IN PARTICULAR PRENAL
    11.
    发明申请
    PROCESS FOR PREPARING 3-SUBSTITUTED 2-ALKENALS, IN PARTICULAR PRENAL 有权
    制备3-取代的2-ALKENALS,特别是预处理的方法

    公开(公告)号:US20140323770A1

    公开(公告)日:2014-10-30

    申请号:US14360323

    申请日:2012-11-23

    Applicant: BASF SE

    CPC classification number: C07C45/66 C07C45/002 C07C45/29 C07C47/21 C07C47/20

    Abstract: The present invention to a process for preparing 2-alkenals of the formula I in which R1 is selected from hydrogen and C1-C4-alkyl; and R2 is selected from hydrogen, C1-C12-alkyl, C2-C12-alkenyl, C4-C8-cycloalkyl and C6-C10-aryl, wherein C1-C12-alkyl and C1-C12-alkenyl may be substituted with C5-C7-cycloalkyl or C5-C7-cylcoalkenyl; comprising dehydrogenating an alkenol of the formula II, an alkenol of the formula III or a mixture thereof, wherein R1 and R2 are each as defined above, wherein the alkenol II, the alkenol III or a mixture thereof is brought into contact with a catalytic system comprising at least one ligand and a metal compound selected from ruthenium(II) compounds and iridium(I) compounds, and wherein the hydrogen formed during the dehydrogenation is removed from the reaction mixture by: v) reaction with a reoxidant selected from C3-C12-alkanones, C4-C9-cycoalkanones, benzaldehyde and mixtures thereof; and/or vi) purely physical means.

    Abstract translation: 本发明涉及一种制备式Ⅰ的2-烯烃的方法,其中R 1选自氢和C 1 -C 4 - 烷基; 并且R 2选自氢,C 1 -C 12 - 烷基,C 2 -C 12 - 烯基,C 4 -C 8 - 环烷基和C 6 -C 10 - 芳基,其中C 1 -C 12 - 烷基和C 1 -C 12 - 烯基可以被C 5 -C 7 环烷基或C5-C7-环基烯基; 包括使式II的烯醇脱氢,式III的烯醇或其混合物,其中R1和R2各自如上所定义,其中链烯醇II,链烯醇III或其混合物与催化体系接触 包括至少一种配体和选自钌(II)化合物和铱(I))化合物的金属化合物,并且其中通过以下步骤从反应混合物中除去在脱氢过程中形成的氢:v)与选自C 3 -C 12 - 烷基酮,C 4 -C 9 - 环烷基酮,苯甲醛及其混合物; 和/或vi)纯粹的物理手段。

    PROCESS FOR PREPARING AND PURIFYING SALTS OF ACRYLAMIDO-2-METHYLPROPANESULFONIC ACID
    12.
    发明申请
    PROCESS FOR PREPARING AND PURIFYING SALTS OF ACRYLAMIDO-2-METHYLPROPANESULFONIC ACID 有权
    丙烯酰胺-2-甲基丙烯酸的制备和纯化工艺

    公开(公告)号:US20130137893A1

    公开(公告)日:2013-05-30

    申请号:US13687156

    申请日:2012-11-28

    Applicant: BASF SE

    CPC classification number: C07C303/22 C07C303/32 C07C303/44 C07C309/15

    Abstract: A process for preparing salts of acrylamido-2-methylpropanesulfonic acid (A) using the steps of: preparing a solution of a contaminated salt of acrylamido-2-methyl-propanesulfonic acid (A) in an anhydrous organic solvent (L) using at least one basic component (B) selected from the group of alkali metal oxides, alkaline earth metal oxides, alkali metal hydroxides, alkaline earth metal hydroxides and amines of the formula (I) NRaRbRc  (I) where the Ra, Rb and Rc radicals are each independently: hydrogen, C1-C4-alkyl, hydroxy-C1-C4-alkyl or C1-C4-alkoxy, where the molar ratio of compound (A) to the basic component (B) is 1:1 to 1:3, recovering the dissolved salt of compound (A) by crystallization or by precipitation, by altering the temperature and/or the pressure and/or the concentration of the salt in the solution. This leads to salts which are low in by-products and are particularly suitable for polymerization.

    Abstract translation: 一种使用以下步骤制备丙烯酰氨基-2-甲基丙磺酸(A)的盐的方法:使用至少在无水有机溶剂(L)中制备丙烯酰氨基-2-甲基 - 丙磺酸(A)的污染盐的溶液 选自碱金属氧化物,碱土金属氧化物,碱金属氢氧化物,碱土金属氢氧化物和式(I)NRaRbRc(I)的胺的一种碱性组分(B),其中R a,R b和R c基团各自为 独立地:氢,C1-C4-烷基,羟基-C1-C4-烷基或C1-C4-烷氧基,其中化合物(A)与碱性组分(B)的摩尔比为1:1至1:3,回收 化合物(A)的溶解盐通过结晶或沉淀,改变溶液中盐的温度和/或压力和/或浓度。 这导致副产物低的盐,特别适用于聚合。

    CONTINUOUS PROCESS FOR PREPARING MENTHOL IN PURE OR ENRICHED FORM
    16.
    发明申请
    CONTINUOUS PROCESS FOR PREPARING MENTHOL IN PURE OR ENRICHED FORM 审中-公开
    用于制备纯净或增强形式的MENTHOL的连续方法

    公开(公告)号:US20140158515A1

    公开(公告)日:2014-06-12

    申请号:US13790465

    申请日:2013-03-08

    Applicant: BASF SE

    Abstract: The present invention relates to a continuous process for preparing racemic or optically active menthol in pure or enriched form by distillatively separating menthol from substance mixtures which comprise essentially menthol and diastereomers thereof. This distillative separation is performed in a dividing wall column with 50 to 300 theoretical plates and one or more side draw points at an absolute operating pressure of 5 to 500 mbar.

    Abstract translation: 本发明涉及通过将薄荷醇与基本上含有薄荷醇和非对映异构体的物质混合物蒸馏分离来制备纯的或富集形式的外消旋或光学活性薄荷醇的连续方法。 该蒸馏分离在具有50至300个理论塔板和一个或多个侧向牵引点的分隔壁塔中进行,其绝对操作压力为5至500毫巴。

    Method for the production of 4,4′-[1-(trifluoromethyl)alkylidene]-bis-(2,6-diphenylphenols)
    19.
    再颁专利
    Method for the production of 4,4′-[1-(trifluoromethyl)alkylidene]-bis-(2,6-diphenylphenols) 有权
    制备4,4' - [1-(三氟甲基)亚烷基] - 双(2,6-二苯基苯酚)

    公开(公告)号:USRE46151E1

    公开(公告)日:2016-09-20

    申请号:US14321865

    申请日:2014-07-02

    Applicant: BASF SE

    Abstract: The present invention relates to a process for preparing 4,4′-[1-(trifluoromethyl)alkylidene]bis(2,6-diphenylphenols), in particular for preparing 4,4′-[1-(trifluoromethyl)ethylidene]bis(2,6-diphenylphenol), which comprises the self-condensation of cyclohexanone in the presence of a basic catalyst to form tricyclic condensation products, dehydrogenation of the resulting tricyclic condensation products in the presence of a supported transition metal catalyst in the condensed phase to form 2,6-diphenylphenol and reaction of the 2,6-diphenylphenol with a trifluoromethyl ketone. The invention further provides an improved process for preparing 2,6-diphenylphenol by aldol self-condensation of cyclohexanone.

    Abstract translation: 本发明涉及一种制备4,4' - [1-(三氟甲基)亚烷基]双(2,6-二苯基苯酚)的方法,特别是制备4,4' - [1-(三氟甲基)亚乙基]双( 2,6-二苯基苯酚),其包括环己酮在碱性催化剂存在下的自缩合以形成三环缩合产物,所得三环缩合产物在冷凝相中负载的过渡金属催化剂存在下脱氢形成 2,6-二苯基苯酚和2,6-二苯基苯酚与三氟甲基酮的反应。 本发明还提供了通过环己酮的醛醇自缩合制备2,6-二苯基苯酚的改进方法。

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