• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The invention relates to a process for the preparation of lactames according to the so-called "Beckmann rearrangement" which consists in isomerizing oximes in a sulfuric solution, the weight ratio percentage of sulfuric acid to the combined amount of sulfuric acid and water being raised to a value above that of the sulfuric solution feed.
    公开号:SU938741A3
    申请号:SU792729503
    申请日:1979-02-16
    公开日:1982-06-23
    发明作者:Мишель Жан-Клод；Потен Филипп
    申请人:Ато Шими(Фирма)；
    IPC主号:
    专利说明:

    3S photonitrization, during the reaction of the rearrangement of the sulfate solution of the oxime, the acid titer of the latter is increased from its initial value of 85-87 to 89-95% by removing part of the water contained in the reaction medium. This removal can be carried out by evaporating the water or applying a vacuum to the reaction medium, or by using a stream of dry inert gas through the reaction medium. In particular, incomplete evaporation of water can be accomplished by applying a more or less deep vacuum in the reactor in which the rearrangement is carried out, or in a flame vessel placed in the circulation chain of this reactor. When a stream of dry inert gas is used to evaporate water and transport it either directly to the reactor or to a flame vessel, the vacuum may be less deep than in the absence of such a gas stream. The invention is based on the fact that the vapor pressure of a mixture of sulfuric acid, water and lactam is significantly higher than that of a mixture of sulfuric acid and water having the same acid titer. In addition, the amount of sulfuric acid in a pair in equilibrium with a mixture containing lactam is significantly less than in a pair in equilibrium with a simple mixture of sulfuric acid and water having the same acid titer. These two properties, namely, increasing the vapor pressure and reducing the concentration of sulfuric acid in the steam, are very beneficial for the partial evaporation of water contained in the reaction medium, especially in the temperature range that usually prevails when using the Beckmann rearrangement. Tab. 1 illustrates these phenomena. Table 1
    . concentration of 90.5% 170
    25% dodecalactam at a concentration of 90.5% 173
    The increase in acid titer can also be accomplished by evaporation of water and the simultaneous addition of sulfuric anhydride or oleum.
    The proposed method has the following advantages in comparison with the known methods: thermodynamic conditions of evaporation are favorable; the increase in acid titer is carried out without additional reagent consumption; the method allows an increase in the acid titer, and this does not lead to the formation of an additional amount of sulphate.
    In the process, the corresponding initial concentrations of the reacting products are chosen so that the concentration of lactam in the final reaction medium is 5-50%, preferably 15 35% by weight.
    18 0.71
    18,167
    The reaction temperature is 80-200 ° C, preferably 120-180. The reaction time is 0.5-60 minutes, preferably 5-20 minutes.
     FIG. Figures 1 and 2 illustrate an optically variants of the device for carrying out the method.
    Example. The device (Fig. 1) contains a reactor 1 heated by an oil circulating in the casing 2. This reactor is equipped with a stirrer 3 and a pipeline i for introducing the oxime oxalic acid solution being treated. The inside of reactor 1 is under reduced pressure using vacuum 5. Volatile products are cooled in heat exchanger 6 and taken in trap 7. The reaction mixture flows through siphon 8 and is taken in cylinder 9 which has the same pressure that prevails in the upper
    parts of the reactor 1, with the help of the pipeline section 10.
    In order to select a given amount of lactam solution from a balloon 9, a reduced pressure is installed in the balloon 11 using a pipe section 12, while the valve 13 is opened for this purpose, while the corresponding valves It-lS are closed Example 2. The device (FIG. 2) contains the reactor 1, heated with the aid of the jacket 2 and equipped with a stirrer 3, is also a pipeline for the continuous introduction of the treated oxime sulfate solution.
    wow. The opening of the valve 14 allows the reaction product to flow into the lower cylinder 11, from where it can then be removed due to the valves 15 and 16 by returning to the atmospheric pressure, and the valves 13 must be closed.
    In tab. 2 shows the working conditions and properties of the final lactam. table 2
    Submerged pipe 5 supplies nitrogen at a rate controlled in a predetermined manner. The discharge opening 6 provides for the removal of a gaseous mixture of nitrogen, water and volatile products. The resulting solution of lactam is 79387 118
    It is continuously siphoned by 7 and the source conditions and properties of the final product are taken in receiver 8. Data on the ralactam are given in Table. 3 Formula of Invention
    The method of producing dodecalactam by isomerizing the cyclododecananoxime sulfate solution obtained by photonitrosis of cyclododecanone under conditions of backman rearrangement with an increase in the acid titer of the mixture after the photonitrization stage is different in that, in order to simplify the process, the increase in the acid titer of the mixture with
    Table 3
    85-87 TO 89-95 are carried out by concentration by heating under vacuum or purging with a dry inert gas.
    Sources of information taken into account in the examination
    1. Zakharkin L. I. Getting ate; -Dodecolactam from cyclododecatriene-1, 5.9. - Neftekhimi, T. 2, 19b2, M 1, p. 106-109 (prototype).
    2. US patent If, cl. 260-239.3, pub. 1975L / X

    Fig z
    权利要求:
    Claims (1)
    [1]
    Claim
    A method of producing dodecalactam by isomerization of a cyclododecanonoxime sulfate solution obtained by photonitrosation of cyclododecanone under Beckman rearrangement with an increase in the acid titer of the mixture after the photonitrization step, characterized in that, in order to simplify the process, the acid titer of the mixture is increased from 45 85-87 ^ to 89 ~ 95% is carried out by concentration by heating under vacuum or by blowing with a dry inert gas.
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    同族专利:
    公开号 | 公开日
    JPH0146506B2|1989-10-09|
    DE2905680A1|1979-08-30|
    FR2417501B1|1981-01-09|
    FR2417501A1|1979-09-14|
    DE2905680C2|1987-06-04|
    JPS54148794A|1979-11-21|
    IT1114203B|1986-01-27|
    JPS6365661B2|1988-12-16|
    JPS62223167A|1987-10-01|
    GB2014572B|1982-07-14|
    GB2014572A|1979-08-30|
    CH636083A5|1983-05-13|
    IT7920244D0|1979-02-16|
    US4211700A|1980-07-08|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    CH237392A|1941-12-05|1945-04-30|Ag Bata|Method and device for the production of isoximes.|
    FR889048A|1941-12-16|1943-12-29|Bata Ag|Process for preparing isoximes|
    FR895509A|1942-06-25|1945-01-26|Ig Farbenindustrie Ag|Process for preparing lactams|
    US3060173A|1958-05-30|1962-10-23|Basf Ag|Production of omega-amino dodecane acid lactam|
    GB923302A|1959-05-13|1963-04-10|Commercial Solvents Corp|Improvements in and relating to the production of lactams|
    US3090739A|1959-07-20|1963-05-21|Toyo Rayon Co Ltd|Method of producing nitroso compounds or oximes|
    FR1256855A|1960-05-12|1961-03-24|Commercial Solvents Corp|Manufacturing process for lactams|
    GB1010152A|1962-05-04|1965-11-17|Toyo Rayon Co Ltd|Preparation of cyclododecanone oxime hydrochloride and ªÏ-lauric lactam|
    US3297684A|1963-01-24|1967-01-10|Toyo Rayon Co Ltd|Photochemical process for the preparation of lactams|
    FR1371942A|1963-07-30|1964-09-11|Organico|Improvement in the process for preparing cycloalkanone oximes and lactams in a concentrated acid medium|
    US3914217A|1974-11-13|1975-10-21|Allied Chem|Process for the preparation of lactams|TW223622B|1991-05-21|1994-05-11|Sumitomo Chemical Co|
    FR2784102B1|1998-09-21|2000-12-08|Atochem Elf Sa|PROCESS FOR THE PREPARATION OF LACTAMS FROM CORRESPONDING OXIMATED CYCLOALCANONE|
    FR2784103B1|1998-09-21|2000-12-08|Atochem Elf Sa|PROCESS FOR PREPARING LAURYLLACTAM BY PHOTONITROSATION OF CYCLODODECANE AND TRANSPOSITION OF BECKMANN IN THE PRESENCE OF METHANESULPHONIC ACID|
    FR2931478B1|2008-05-26|2012-08-03|Arkema France|PRODUCT FOR PREPARING LACTAMS COMPRISING A PHOTONITROSATION STEP FOLLOWED BY A BECKMANN TRANSPOSITION STEP|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FR7804571A|FR2417501B1|1978-02-17|1978-02-17|
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