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    • 1. 发明专利
    • Preparation of unsaturated fatty acid
    • 不饱和脂肪酸的制备
    • JPS59116247A
    • 1984-07-05
    • JP22504282
    • 1982-12-23
    • Soda Koryo Kk
    • NAMITA TAKESHIETOU TAKEAKISUZUKI KIYONORISHIRAKAWA TOSHIBUMI
    • C07C57/03B01J21/16B01J29/00B01J29/06B01J31/02C07B61/00C07C51/00C07C51/09C07C67/00
    • Y02P20/52
    • PURPOSE: To obtain an unsaturated fatty acid useful as a material for blended spice for foods under relatively mild conditions by a short process economically, easily, in high yield, by heating an easily obtainable lactone as a raw material in the presence of an acid catalyst.
      CONSTITUTION: A lactone such as ε-decalactone, etc. shown by the formula I (n is 3 or 4; R is 1W10C alkyl or alkenyl) is heated in the presence of an acid catalyst at 100W300°C, especially preferably 150W250°C, and further distilled to give the desired compound such as 5- and 6-decenoic acid, etc. shown by the formula II (either of wavy lines is dobule bond). Activated clay, p-toluenesulfonic acid, benzenesulfonic acid, sulfuric acid, phosphoric acid, etc. may be cited as the acid catalyst, and an amount of it used is 0.1W10wt% based on the lactone shown by the formula I .
      COPYRIGHT: (C)1984,JPO&Japio
    • 目的:通过在酸性催化剂的存在下,通过加热容易获得的作为原料的内酯,经济地,容易地以高产率获得在相对温和的条件下用作食品的混合香料用作食品的不饱和脂肪酸 。 构成:式I(n为3或4; R为1-10C烷基或链烯基)所示的内酯如ε-癸内酯等在酸催化剂存在下在100-300℃加热, 特别优选150-250℃,并进一步蒸馏,得到式II所示的所需化合物如5-和6-癸烯酸等(波浪线为多巴胺键)。 可列举活性粘土,对甲苯磺酸,苯磺酸,硫酸,磷酸等作为酸催化剂,其使用量相对于式I所示的内酯为0.1-10重量%。
    • 2. 发明专利
    • Preparation of 3,5,5-trimethyl-2-cyclohexen-1-one derivative
    • 3,5,5-三甲基-2-环己基-1-酮衍生物的制备
    • JPS58198434A
    • 1983-11-18
    • JP8007182
    • 1982-05-14
    • Soda Koryo Kk
    • NAMITA TAKESHIETOU TAKEAKISUZUKI KIYONORIITOU NOBUHIKO
    • C07C67/313C07C45/00C07C45/51C07C49/603C07C49/757C07C67/00C07C69/738C07C231/00C07C231/12C07C235/78C07C253/00C07C255/31
    • PURPOSE: To prepare the titled substance in short steps, by reacting 3,5,5-trimethyl-2-cyclohexen-1-one magnesium enolate with an olefinic compound, hydrolyzing the reaction product, and if necessary, treating with an acid or a base.
      CONSTITUTION: The compound of formula III is prepared by reacting the compound of formula I (X is halogen) with the compound of formula II [R
      1 and R
      2 are H or 1W5C aliphatic hydrocarbon group; Y is -C(=0)R
      3 , -COOR
      4 or -CONR
      5 R
      6 (R
      3 , R
      5 and R
      6 are H or 1W5C aliphatic hydrocarbon group; R
      4 is 1W5C aliphatic hydrocarbon group] at a molar ratio of 1:(1W1.5) at -20W +5°C, hydrolyzing the reaction product to remove magnesium, and if necessary, treating the hydrolyzate with an acid or a base.
      EFFECT: The objective compound can be prepared in high yield with simple operation.
      USE: Flavor for food, drink, cosmetic, tobacco, etc. Intermediate of carotinoid, perfumery, pharmaceuticals, etc.
      COPYRIGHT: (C)1983,JPO&Japio
    • 目的:为了以短时间步骤制备标题物质,通过使3,5,5-三甲基-2-环己烯-1-酮镁烯醇化物与烯烃化合物反应,水解反应产物,如果需要,用酸或 基础。 结构式:式III化合物通过使式I化合物(X为卤素)与式Ⅱ化合物反应制备:[R 1和R 2]为H或1-5C脂族烃基; Y是-C(= O)R 3,-COOR 4或-CONR 5 R 6(R 3,R 5和R 6)是H或1-5C脂族基 烃基; R 4为1-5C脂肪族烃基],在-20〜+ 5℃下摩尔比为1:(1-1.5),水解反应产物以除去镁,如果需要, 使用:食品,饮料,化妆品,烟草等的中等程度的类胡萝卜素,香料,药物等的中间体。