• 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:
    A thiophenol is produced by a process which consists in reacting hydrogen sulfide and a source of hydrogen with a halogenated aromatic compound. The total conversion of the reaction is improved by increasing the reaction temperature as the total conversion decreases optionally independently of the presence of hydrogen. The process produces high yields of thiophenol with low quantities of byproduct aromatic thioethers, particularly diphenyl disulfide.
    公开号:SU1222192A3
    申请号:SU802901345
    申请日:1980-04-01
    公开日:1986-03-30
    发明作者:Эдвард Скжеч Адам
    申请人:Стауффер Кемикал Компани (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to an improved method for the preparation of hisphenol and its variant, which finds use as an intermediate product in the synthesis of biologically active substances and polymers,
    The aim of the invention is to increase the yield of the target product. The invention is illustrated by the following examples.
    Example 1. In the course of the experiment, the reaction apparatus is used in the form of a tube. with an internal diameter of 1 inch (2.54 cm) and a height of 5.5 feet (1.67 m) with a catalytic onoeii. The catalytic layer consists of A2A g (layer height 5 feet, 1.52 m), 3.08 liters of activated carbon (6x16) PPG. The temperature of the bed is due to heating through it. Comparative examples. It is carried out as in Example 1, except that a stream of hydrogen is not supplied to the catalytic layer, while

    The degree of conversion of monochlorobenzene,%, in:
    RSH I
    40 100 150 200 300
    I
    adjusted to pressure
    Monochlorobenzene is uniformly passed through the catalytic bed at a flow rate of 71 g / h, 0.63 mol / h.
    Hydrogen sulfide evenly Pass through the catalytic layer with a flow rate of 64 g / h, 1.89 mol / h. Before being fed into the catalytic layer, hydrogen sulphide is heated to, Gaseous hydrogen is introduced into the hydrogen sulphide stream at a flow rate of 0.39 g / h, 19 yol / h before heating. The molar ratio between hydrogen sulfide, monochlorobenzene and hydrogen is 3: 1: 0.3.
    The reaction is carried out continuously for 300 hours.
    The results are shown in Table 1. “T a b l and c a I
    temperature of the catalytic layer is C50, pressure is atm.
    The results are shown in Table 2. Table 2
    Total degree of conversion per cycle,%


    39.0 28.4 26.5 24.6 20.0
    Uh
    EXAMPLE 2 The experiment of this winner is carried out in a battery-scale reaction system with hot fixed singing in tubes, which includes a group of AO tubes of 1 inch x 6 feet (2.5A cm X cm). The tubes are made of stainless steel and Inkolo 825 alloy. As a gas distributor, a 316 stainless steel disc with 21 holes of 1/16 inch, 1.59 mm is used.
    The heat of reaction dp is supplied by external heaters, suspended from n chrome wire, supplied with insulating beads. The temperature of the catalytic unit is maintained at. constant level by adjusting the supply of electricity to the wire of the heaters. Each reaction apparatus is equipped with 5 pairs for fixing and controlling the temperature. Reagents are fed to individual feeds6 15 20 25 30
    0
    221924
    m passing through the side of the air box, which allows for homogeneous contacting. pre-heated hydrogen sulfide and chlorobenzene before passing through the distribution plate and layer of activated carbon. The reaction off-gases are condensed in a two-pass stainless steel refrigerator and collected in a glass receptacle. The ventilation lines of both reaction vessels are equipped with valve means, which allow one to collect condensate from either the two reaction devices or from each reaction device separately.
    (.
    In the course of conducting one experiment (duration 32 hours), methane, which served as a source of hydrogen, is used instead of hydrogen, with the temperature of the catalytic layer being at least 1 atm. Table3
    five
    0
    In the product found small. the amount of mercaptan that was formed by the following reactions:
    PRI me R 3. The experiment was carried out similarly to Phim 1.
    A layer of freshly activated carbon catalyst is placed in the reaction apparatus. Initially, the reaction is carried out at AOO with. The reaction apparatus is divided into three heating zones of different
    heights. For the Caldah, a zone around the reaction apparatus is provided. An electrical resistance heater is made of nichrome wire. Since this reaction is only a few thermally isothermal conditions of the reaction, support is maintained by controlling the supply of electricity to each heating zone. It has been established that by regulating the supply of electricity, the temperature in the reaction zone can be maintained in the interval i 5 C.
    Using such a fresh layer of activated carbon, the initial degree of conversion sa is achieved.
    5} 2221926
    one 11KL is equal to approximately A)%. for the next 16 hours it will increase
    Then, the overall conversion rate is up to about 25%. Upon expiration
    for the next 240 hours, I gradually gradually increase to approximately 80 more hours, to approximately the level of conversion again decreases to
    20%. During the next 20Z,
    It was established by experiments that thereafter the temperature of the catapic case, if the reaction is carried out, is raised to. As a result, the overall conversion rate in the total conversion rate is an increase of an additional 60 hours, i.e. up to approximately 25%. By expiry, 300 hours is approximately 80 more hours.
    from 5 to 7%. The overall degree of con-general conversion decreases
    version, less than 14%, is considered to be approximately 20%. : unaccountable. This process is repeated a few more times until the temperature of the catalytic layer of the not reaching the catalytic layer is increased to 240 ° C after 240 hours. Found that for
    (by increasing the amount of flow of such a reaction in the indicated electricity in each zone conditions, this temperature is heated). The overall conversion rate in jq is max.
    权利要求:
    Claims (4)
    [1]
    B A method for the preparation of thiophenol by the interaction of halogenbenzene with hydrogen sulfide in the presence of a carbon catalyst when heated, which consists in the fact that, in order to increase the yield of the target product, the process is carried out in the presence of hydrogen or methane as a source of hydrogen at 45 ° C.
    [2]
    2. The method of pop. 1, characterized in that chlorobenzene is used as halobenzene.
    [3]
    3. The method for producing a thiophenol by reacting halobenzenes with hydrogen sulfide in the presence of a carbon catalyst under heating, characterized in that, in order to increase the yield, the process is carried out by increasing the process temperature from 400 to 520 C as reduction in the overall degree of conversion.
    [4]
    4. The method according to p. and with the fact that chlorobenzene is used as halobenzene.
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    同族专利:
    公开号 | 公开日
    AT3857T|1983-07-15|
    DD149936A5|1981-08-05|
    CA1153016A|1983-08-30|
    KR830001883A|1983-05-19|
    HU185786B|1985-03-28|
    IL59616A|1984-10-31|
    EP0018118A2|1980-10-29|
    PH15912A|1983-04-22|
    DE3063825D1|1983-07-28|
    KR850001372B1|1985-09-24|
    MX6660E|1985-10-02|
    ES8104217A1|1981-04-01|
    EP0018118B1|1983-06-22|
    IL59616D0|1980-06-30|
    JPS646188B2|1989-02-02|
    EP0018118A3|1981-05-06|
    ES490129A0|1981-04-01|
    BR8001818A|1980-11-18|
    JPS55133353A|1980-10-17|
    DK135280A|1980-10-03|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US2402686A|1940-04-13|1946-06-25|Du Pont|Hydrogenation of aryl sulphides and products resulting|
    US2490257A|1946-05-15|1949-12-06|Socony Vacuum Oil Co Inc|Mono-and polyalkyl mono-and polynuclear mercaptans|
    US3994980A|1975-10-15|1976-11-30|Phillips Petroleum Company|Cobalt molybdate as catalyst for preparation of mercaptans from carbonyl compounds hydrogen sulfide and hydrogen|US4540830A|1981-03-02|1985-09-10|Cornell Research Foundation, Inc.|Anti-juvenile hormones|
    US4347256A|1981-03-02|1982-08-31|Cornell Research Foundation, Inc.|Anti-juvenile hormones|
    CN1164527C|2000-07-28|2004-09-01|株式会社村田制作所|Ceramic paste composition, ceramic forming body and ceramic electronic element|
    JP5312192B2|2009-05-18|2013-10-09|住友精化株式会社|Aromatic thiol compound and method for producing aromatic sulfide compound|
    CN104829507B|2015-05-06|2017-08-18|山东豪迈化工技术有限公司|Without the method that fragrant thiophenol is produced under catalyst action|
    WO2017221340A1|2016-06-22|2017-12-28|本多電子株式会社|Ultrasonic sensor unit, method for manufacturing same, and ultrasonic measuring device|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US2613979A| true| 1979-04-02|1979-04-02|
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