• 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:
    P-Amino phenols of formula (I) wherein R1 and R2 are independently hydrogen, optionally substituted alkyl, halogen, COOH, SO3H or NO2, are produced by electrolytic reduction of p-phenylazophenola of formula (II) wherein R1 and R2 are as defined above, in an aqueous basic medium at a pH value at least equal to the pKa value of the p-phenylazophenol and at a temperature of at least 50<o>C preferably 70 to 100<o>C. The compounds (I) can hereby be produced without problems, in particular of an environmental nature, which are associated with the chemical reducing methods. The process is particularly useful for the preparation of the compound 5-aminosalicylic acid which is a valuable active component of certain medicaments for the treatment of colitis ulcerose and Crohn's disease.
    公开号:SU1493101A3
    申请号:SU864027853
    申请日:1986-07-21
    公开日:1989-07-07
    发明作者:Лунд Хеннинг
    申请人:Фармацеутиск Лабораториум Ферринг А/С (Фирма)；
    IPC主号:
    专利说明:

    This invention relates to an improved process for the preparation of 4-aminophenols of formula 1
    where R and R are each hydrogen, halo, or carboxyl groups.
    The aim of the invention is to simplify the process.
    Example 1. Preparation of 5-aminosalicylic acid.
    A. Preparation of 5-phenolazosalicylic acid
    18.6 kg (200 mol) of aniline are dissolved in a mixture of 40 liters of concentrated hydrochloric acid and 45 liters of water with stirring. Cooling is performed to 0 ° C and a solution of 14 kg of sodium nitrite
    in DO L water is slowly added with good stirring so that the temperature does not exceed 2 ° C. After the addition is complete, stirring is continued for another 15 minutes, and then about 4 kg of anhydrous sodium carbonate is added in small portions with stirring. The pH value is between 1 and 2.
    In the third container (C), 28 kg (202 mol) of salicylic acid are dissolved in 33 l of concentrated sodium hydroxide solution (500 g of NaOH in 1 l of solution) and 67 l of water, in which 2 kg of anhydrous sodium carbonate is added. After cooling, the contents are pumped out slowly and with stirring from the container (A) to the container (C) so that the temperature is kept lower. Azo compound gradually falls out

    WITH
    OO

    s
    31
    into the sediment and finally becomes empty porridge-like mass. The last part of the coupling reaction flows slowly and the mass must be stirred for 5 or 6 hours after the addition of the diazo compound solution from container (A) has been completed.
    B. Reduction of 5-phenylazosalicylic acid,
    20 liters of a concentrated solution of sodium hydroxide (500 g of NaOH in 1 l of solution) are added to the contents of the container (C) and heating is carried out until the entire mass is dissolved and the pH value reaches above 12. Then the contents are pumped to another the container (D), followed by heating to 80 ° C. The content is pumped through an electrolysis cell, which can be a filter-type electrolyzer with a lead cathode potential of at least 1.4. B (measured relative to the standard calomel electrode). The current density is 10–20 A / dm. After 20,000, the current density decreases to 2–3 A / dm, and after an additional 2 hours the electrolysis stops. The solution is provided by the addition of 5 kg of sodium hydrosulfite and is pumped into a container (F), purged throughout the volume with aeotome.
    In a 250 liter of water, 40 kg of NaOH are dissolved in a container (E) and the solution is used as an anode liquid. In order to preserve the anodes, it is important that the solution always be strongly basic.
    Water vapor (optionally overheated steam) is passed through the contents of the conveyor (F) and the resulting aniline is distilled off along with the water vapor. Concentrated hydrochloric acid is then added until the pH is 4.1 and the cooling is carried out with stirring. After a couple of hours, crystallization is completed and the resulting 5-aminosalicylic acid is added by centrifugation or to a filter press. The yield is approximately 28 kg of slightly reduced C of a substance that is purified by recrystallization from water, followed by decolouration with activated carbon.
    Examples 2-7. Electrolytic production of 5-aminosalicylic acid is studied with various conditions.
    11BULTIES in these examples. For each electrolysis, 0, 4-mol of 5-phenylazosalicylic acid is used and the process is carried out as follows.
    In a mixture of 160 ml of concentrated hydrochloric acid and 180 ml of desalted water, 74.5 g of double-distilled aniline are dissolved with stirring, and then the solution is cooled to 0 ° C in an ice-salt bath. 56 g of NaNO 1 are dissolved in 160 ml of desalted water and the solution is cooled to 0 ° C and then slowly added with stirring to the solution of aniline chloride so that the temperature does not exceed 2 ° C. After completion of the addition, the pH is 1.0-1.5.
    In a mixture of 132 ml of a concentrated solution of NaOH (500 g in 1 l of the solution) and 268 ml of water are dissolved with stirring 112 g of salicylic acid.
    After cooling to OC, the diazoconnection is added slowly with stirring so that the temperature does not exceed 3 ° C. The resulting combination reaction product is a viscous mass that is stirred overnight.
    The resulting azo compound (0.8 mol) is mixed with a mixture of concentrated NaOH and water to dissolve the product of the coupling reaction before electrolysis. At the same time, the pH value is exceeded 12. The amount of azo compound obtained is sufficient for carrying out two electrolysis operations.
    Half of the amount of the solution (corresponding to 0.4 mol of 5-phenyl-azscalicylic acid) is poured into the cathode chamber of the electrolysis cell. The NaOH solution is poured into the anode chamber. Content is pumped through the electrolysis cell. After completion of the electrolysis, the recovered reaction product is placed in a flask. Cool down and add HCl to pH 4.0. After filtration, the residue (5-aminosalicylic acid) is washed in HjO and acetone.
    The electrolysis is carried out in a standard electrolysis cell, in which the anodic and cathodic chambers are separated using a semipermeable membrane. The cathode is lead, and the anode is nickel. Cathode electrode
    comparison is Ag / Ag Cl-electrode.
    The standard voltage should be higher than 0.8 V, which is the natural potential of an electrode of the type Ag / Ag C1. The standard voltage below this value means that no reduction will occur. The standard voltage should be as close to 1.5 V as possible, and should be maintained at this value in order for the recovery to proceed satisfactorily.
    The electrolysis conditions used are shown in the table. In addition, the yield of crude 5-aminosalicylic acid, obtained with each electrolysis, is presented in the table.
    In example 2, due to the relatively low reaction temperature of 60 ° C, the standard voltage reaches only 1.2 V (but not during the entire reaction time). This causes a deterioration in the reaction process and therefore the reaction must proceed at a temperature of at least 70 ° C. The high yield of the reaction product in Example 2 is probably due to the relatively high unreliability associated with the test, because the quantities involved were very small.
    Example 8, Obtaining para-aminophenol,
    In an Fl-shaped cell, consisting of two 250-millimeter conical flasks connected through a semipermeable membrane and fitted with a mercury cathode and a carbon anode, the cathode chamber is filled with a solution of 10 g of oxyazobenzene vapor in 150 ml of 0.2 M sodium hydroxide solution the pH is above 12 and the anode chamber is filled with a 0.5 M sodium hydroxide solution. The cathode chamber is provided with a thermometer and reflux condenser. The nitrogen is supplied and the nitrogen atmosphere is maintained in the cathode chamber for
    complete recovery. The temperature is increased to and electrically where R, and each hydrogen, halogen or carboxyl group, by electrolytic reduction of phenol derivatives in water in the presence of an alkali metal hydroxide, is characterized in that, in order to simplify the process, the corresponding p-phenyl-eophenol is used as a derivative of phenol
    The rolysis was carried out at -1.2 V, measured against a standard calomel electrode, with stirring with a magnetic stirrer. The initial and process is carried out at 60-80 ° C and the pH on the current density is equal to at least 10 A / dm. It gradually decreases to allow p-phenylazophenol, and the solution changes from keeping the process in solution.
    five
    transparent to very slightly colored color (pale brown). The reflux condenser is replaced with a distillation apparatus and most of the analysis obtained is distilled off, and the temperature is about the same. The azo-pa stream and water vapor transfer the aniline to the receiving flask.
    The cathode fluid is cooled and neutralized to a pH of about 6.5. After standing at 0 ° C, A, 6 g (84%) of para-aminophenol is filtered off in the form of slightly pale brown crystals.
    , PR and M 9. 9. Preparation of 2-chloro-3-aminophenol.
    10 g of 4-phenylazo-2-chlorophenol is reduced in the same way as in Example 8. The yield is 5, A g (86%) of 2-chloro-4-aminophenol with a melting point of 153 ° C.
    The proposed method allows 5 to simplify the known electrolytic method of producing aminophenols, which involves carrying out the process in an inert atmosphere and using a large number of electrolytic cells.
    The proposed method allows to obtain the target product with good results using only one electrolytic cell, the device of which does not play a decisive role.
    权利要求:
    Claims (1)
    [1]
    Invention Formula
    0
    five
     The method of obtaining p-aminophenol or its derivatives of the general formula
    RI
    H, N.
    he is Ig
    where R and each hydrogen, halogen or carboxyl group, by electrolytic reduction of phenol derivatives in water in the presence of an alkali metal hydroxide, characterized in that, in order to simplify the process, the corresponding p-phenyl Aeophenol is used as a phenol derivative
    and the process is carried out at 60-80 ° C and a pH of at least the pKA value of p-phenylazophenol, which allows the process to be carried out in solution.
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    同族专利:
    公开号 | 公开日
    EP0203122B1|1989-04-26|
    JPS62501218A|1987-05-14|
    ES549140A0|1986-09-01|
    DK553784A|1986-05-23|
    ES8609208A1|1986-09-01|
    EP0203122A1|1986-12-03|
    WO1986003194A1|1986-06-05|
    US4670112A|1987-06-02|
    HUT42057A|1987-06-29|
    DK553784D0|1984-11-22|
    DK153412C|1988-12-19|
    DE3569724D1|1989-06-01|
    DD242640A5|1987-02-04|
    DK153412B|1988-07-11|
    HU199106B|1990-01-29|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US1542265A|1922-10-20|1925-06-16|James F Norris|Process of making aminosalicylic acid|
    US1882758A|1929-03-19|1932-10-18|Dow Chemical Co|Preparation of amino-phenols and primary aryl amines conjointly|
    GB1308042A|1969-05-28|1973-02-21|Brown John Constr|Process for the preparation of rho-amino phenol by the electrolytic reduction of nitrobenzene|
    GB1421118A|1971-11-16|1976-01-14|Albright & Wilson|Electrolytic reduction of nitrosophenols|AT398316B|1989-06-01|1994-11-25|Verein Zur Foerderung Der Fors|METHOD FOR REDUCING DYE|
    DE4020056A1|1990-06-23|1992-01-02|Bayer Ag|METHOD FOR PRODUCING VERY PURE 5-AMINOSALICYL ACID|
    DE10029410A1|2000-06-15|2002-01-03|Bfgoodrich Diamalt Gmbh|Process for the preparation of 5-aminosalicylic acid|
    US8048924B2|2001-08-29|2011-11-01|Biocon Limited|Methods and compositions employing 4-aminophenylacetic acid compounds|
    AT448194T|2000-08-29|2009-11-15|Biocon Ltd|USE OF A PHARMACEUTICAL COMPOSITION COMPRISING A PARA-AMINOPHENYL ACIDIC ACID DERIVATIVE FOR THE TREATMENT OF INFLAMMATORY DISEASES OF THE MAGNETIC STRENGTH|
    CA2359812C|2000-11-20|2004-02-10|The Procter & Gamble Company|Pharmaceutical dosage form with multiple coatings for reduced impact of coating fractures|
    DK1773767T3|2004-07-07|2016-03-21|Biocon Ltd|Synthesis of azo bound in immune regulatory relations|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DK553784A|DK153412C|1984-11-22|1984-11-22|PROCEDURE FOR THE PREPARATION OF P-AMINOPHENOLS BY ELECTROLYSE|
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