Production of alkenones
    1.
    发明授权
    Production of alkenones 失效
    生产碱

    公开(公告)号:US3819713A

    公开(公告)日:1974-06-25

    申请号:US2808070

    申请日:1970-04-13

    Applicant: BASF AG

    CPC classification number: C07C45/75 C07C45/71 C07C49/203

    Abstract: ALKENONES WHOSE OLEFINIC DOUBLE BOND IS IN THE $,E-POSITION OR Y,&-POSITION TO THE KETO GROUP, ARE PREPARED BY REACTION OF AN OLEFIN WITH A B-HYDROXYKETONE IN THE LIQUID PHASE OR IN A SINGLE REACTION STAGE BY REACTION OF AN OLEFIN WITH FORMALDEHYDE OR A COMPOUND YIELDING FORMALDEHYDE AND AN ALIPHAIC KETONE IN THE LIQUID PHASE. ALKENONES ARE INTERMEDIATES FOR THE PRODUCTION OF PERFUMES AND VITAMINS.

    PRODUCTION OF ISOPRENE
    2.
    发明专利

    公开(公告)号:CA937588A

    公开(公告)日:1973-11-27

    申请号:CA84725

    申请日:1970-06-04

    Applicant: BASF AG

    Abstract: 1301037 Isoprene BADISCHE ANILIN- & SODA-FABRIK AG 5 June 1970 [6 June 1969] 27190/70 Heading C5E Isoprene is made by dehydrating 3-methyl-3- buten 1-ol at 200-300‹ C. in the presence of a calcium phosphate catalyst, the 3-methyl-3- buten-1-ol having a purity of at least 85% by wt. of the total oxygen containing starting material. The reaction is preferably carried out in the presence of steam and/or an inert gas.

    4.
    发明专利
    未知

    公开(公告)号:DK122222B

    公开(公告)日:1972-02-07

    申请号:DK72068

    申请日:1968-02-23

    Applicant: BASF AG

    Abstract: 1,208,835. Production of alk-3-en-1-ols. BADISOHE ANILIN- & SODA-FABRIK A.G. 23 Feb., 1968 [25 Feb., 1967 (3); 30 Dec., 1967], No. 8881/68. Heading C2C. Alk-3-en-1-ols are prepared by reacting an olefinically unsaturated hydrocarbon bearing at least one hydrogen atom on at least one carbon atom adjacent to the carbon atoms of the double bond at from 235‹ to 400‹ C. with an aldehyde in the absence of an acid catalyst. By the term "alk-3-en-1-ols" is meant an acyclic or cyclic compound which is an olefinically unsaturated primary or secondary alcohol in which the carbon atom bearing the hydroxy group is separated from the nearest carbon atom bearing a double bond by a single carbon atom. The reaction is preferably carried out in the presence of a base comprising from 0À001 to 10% by weight of the total weight of the reaction mixture. It is not necessary to start from the free aldehyde, and hydrates, acetals, oligomers or polymers of aldehydes may be used. Alcohols which dehydrate under the reaction conditions to olefins may be used in the process as olefin precursors. The reaction may be carried out in the presence of a substance having a large surface area.

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