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    Production of 6,10-dimethylundecatrien-(3,5,10)-one-(2)
    1.
    发明授权
    Production of 6,10-dimethylundecatrien-(3,5,10)-one-(2) 失效
    6,10-二甲基 - （3,5,10） - 酮 - （2）

    公开(公告)号：US3860655A

    公开(公告)日：1975-01-14

    申请号：US9157170

    申请日：1970-11-20

    Applicant: BASF AG

    Inventor： POMMER HORST ,  REIF WERNER ,  PASEDACH HEINRICH ,  HOFFMANN WERNER

    IPC: C07C45/67 ,  C07C49/20 ,  C07C403/00 ,  C07C45/18

    CPC classification number: C07C45/676 ,  C07C67/03 ,  C07C2601/16 ,  C07C49/203 ,  C07C69/72

    Abstract: Production of Beta -ionone by reaction of 3,7-dimethylocten(7)-yn-(1)-ol-(3) with a lower alkanol ester of acetoacetic acid at a temperature of from 100* to 400*C and treating the reaction mixture with an acid catalyst at a temperature of from 100* to 400*C and cyclizing the 6,10-dimethylundecatrien-(3,5,10)-one-(2) obtained by contacting with concentrated sulfuric acid at temperatures of from -30 to +20*C.

    Abstract translation: 通过3,7-二甲基辛 - （7） - 炔 - （1） - 醇 - （3）与乙酰乙酸的低级链烷醇酯在100-400℃的温度下反应制备β-戊酮， 该反应混合物与酸催化剂在100-400℃的温度下反应，并将6,10-二甲基十一碳三烯 - （3,5,10） - 酮（2）与浓硫酸在 -30〜+20℃

    Production of 6,10-dimethylundecatriene-(3,5,10)-one-(2)
    3.
    发明授权
    Production of 6,10-dimethylundecatriene-(3,5,10)-one-(2) 失效
    （3,5,10） - 酮（2）的制备6,10-二甲基 -

    公开(公告)号：US3860654A

    公开(公告)日：1975-01-14

    申请号：US7493970

    申请日：1970-09-23

    Applicant: BASF AG

    Inventor： POMMER HORST ,  REIF WERNER ,  PASEDACH HEINRICH ,  HOFFMANN WERNER

    IPC: C07C45/67 ,  C07C49/20

    CPC classification number: C07C403/16 ,  C07C45/676 ,  C07C67/46 ,  C07C2601/16 ,  C07C49/203 ,  C07C69/72

    Abstract: Production of Beta -ionone by reaction of 3,7-dimethylocten(7)-yn-(1)-ol-(3) with diketene to form the acetoacetic ester of 3,7-dimethylocten-(7)-yn-(1)-ol-(3), decomposing the same at 100* to 400*C in the presence of an acid catalyst and/or after treating the mixture in the presence of the catalyst and cyclizing the 6,10-dimethylundecatrien-(3,5,10)-one-(2) obtained by treatment with concentrated sulfuric acid at temperatures of from -30* to 20*C.

    Abstract translation: 通过3,7-二甲基辛烯（7）-yn-（1） - 醇 - （3）与双烯酮的反应生成β-戊酮，形成3,7-二甲基辛烯（7）-yn-（ 1）-ol-（3），在酸催化剂存在下，在100〜400℃下分解，和/或在催化剂存在下处理混合物后，将6,10-二甲基二十碳三烯（3 ，5,10） - 酮 - （2），通过在-30℃至20℃的温度下用浓硫酸处理得到。

    PREPARATION OF GRANULAR VITAMIN A ESTERS
    8.
    发明专利
    PREPARATION OF GRANULAR VITAMIN A ESTERS 未知

    公开(公告)号：GB1300166A

    公开(公告)日：1972-12-20

    申请号：GB1980270

    申请日：1970-04-24

    Applicant: BASF AG

    Inventor： REIF WERNER ,  NUERRENBACH AXEL ,  FREYSCHLAG HERWIG

    IPC: C07C403/00

    Abstract: 1300166 Granular Vitamin A esters BADISCHE ANILIN- & SODA-FABRIK AG 24 April 1970 19802/70 Heading C2V Granular Vitamin A esters are prepared by dripping molten Vitamin A ester into an organic liquid at -10 to -70‹ C., the liquid being one in which the ester is insoluble and which has a lower density than the esters, the resultant granules then being separated and dried. The liquid may be an alcohol or a gasoline. An antioxidant may be added to the melt. In examples, molten Vitamin A acetate and Vitamin A palmitate are dripped into cooled methanol to form granules.

    Production of Compounds containing an olefinic double bond
    10.
    发明专利
    Production of Compounds containing an olefinic double bond 未知

    公开(公告)号：GB1168639A

    公开(公告)日：1969-10-29

    申请号：GB5642766

    申请日：1966-12-16

    Applicant: BASF AG

    Inventor： REIF WERNER ,  POMMER HORST

    IPC: C07C403/12 ,  C07B37/00

    Abstract: 1,168,639. Double bond synthesis. BADISCHE ANILIN- & SODA-FABRIK A.G. 16 Dec., 1966 [18 Dec., 1965], No. 56427/66. Heading C5E. [Also in Division C2] Compounds containing an olefinic double bond are prepared by continuously contacting a phosphorus ylid with a carbonyl compound in a substantially constant molar ratio and continuously removing the reaction mixture containing the product from the reaction zone. Alternatively a phosphonium salt which yields the phosphorus ylid on reaction with a proton acceptor, may be continuously contacted with a proton acceptor and a carbonyl compound and the reaction mixture removed as before. The reactants are preferably cooled and supplied in liquid or dissolved form, and may be contacted in a mixing nozzle, stirred reactor or a circular tube system. Compounds of the Formula (VII) are formed from the ylid (III) and the carbonyl compound (V) Examples of suitable carbonyl compounds are 2-methyl-2-butenal, #-ionone, citral, 2-methylhept-2-en-one #-ionylidene acetaldehyde and Vitamin A aldehyde. The groups R 1 and R 11 may be C 1 -C 30 saturated or unsaturated aliphatic radicals.

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