• 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:
    Process for the preparation of 1,1-diarylalkanes, which is characterized in that an aromatic compound which has at least one aromatic hydrogen is reacted with an acetal in the presence of a perfluorinated sulfonic acid in polymeric form as a catalyst.
    公开号:BE1019667A3
    申请号:E2011/0003
    申请日:2011-01-06
    公开日:2012-09-04
    发明作者:Jeffrey Howard Dimmit；Mike Douglas Cagle
    申请人:Evonik Degussa Gmbh；
    IPC主号:
    专利说明:

    PROCESS FOR THE PREPARATION OF 1.1 DIARYLALKANES AND DERIVATIVES THEREOF
    The present invention relates to a process for the preparation of 1,1-diarylalkanes by condensation of aromatic compounds with acetals using a perfluorinated sulfonic acid in polymeric form as a catalyst.
    Methods of Making Diarylalkanes are known in the art.
    JP 02-134332 A discloses a process for the preparation of diarylmethanes in which aromatic hydrocarbons and formaldehyde are reacted in the presence of a sulfuric acid catalyst and in the presence of surfactants.
    FR 2745285 A1 discloses the C-alkylation of aromatic compounds using a specific catalyst comprising a rare earth metal on a clay, silica and / or alumina carrier.
    US 4,814,537 A discloses a process for preparing methyl-substituted diphenylmethanes by coupling methyl-substituted benzene by contacting with a solid heterogeneous catalytically-active oxide of vanadium, molybdenum, rhenium and / or tungsten.
    US 4,895,988 A discloses the specific zeolite-catalyzed condensation of aromatic compounds with carbonyl compounds, such as phenol (s) with formaldehyde, to form diarylalkanes.
    US 2003/0013932 A1 discloses a process for preparing diarylmethanes and derivatives thereof using a methylenating agent such as formaldehyde in the presence of a heteropolyacid catalyst.
    Tetrahedron Letters (2006) 47 (14), 2291-2294, discloses the synthesis of diarylmethanes by InCI3-4H20 catalyzed dehydration of electron-rich arenes with trioxane.
    No. 6,207,866 discloses a process for preparing diarylmethane or corresponding derivatives by reacting dimethoxymethane (DMM) with an aromatic compound at a reaction temperature in the range from 80 to 400 ° C. in the presence of an acid catalyst. There it is further disclosed that the DMM can be prepared by reacting an alcohol with formaldehyde in the presence of an acid catalyst.
    The problem with the above-cited prior art is that when substituted aromatic compounds such as xylene are involved in the reaction, the indicated isomer selectivity is poor. In addition, the reaction yields are not acceptable. In the above-referenced US 6,207,866, acidic cation exchange resins such as sulfonated styrene-divinylbenzene copolymer and sulfonated perfluoroethylene copolymer known under the tradename Nation® are listed in the preparation of the above-discussed DMM from an alcohol and formaldehyde.
    The present invention relates to a process for the preparation of 1,1-diarylalkanes, which is characterized in that an aromatic compound having at least one aromatic hydrogen is reacted with an acetal in the presence of a perfluorinated sulfonic acid in polymeric form as a catalyst. It has been found that conversion to 1,1-diarylalkanes with this catalyst proceeds in high yield and with improved isomer selectivity.
    One embodiment of the present invention is a process for the preparation of 1,1-diarylalkanes by condensation of aromatic compounds with acetals using a perfluorinated sulfonic acid in polymeric form as a catalyst.
    The aromatic compound used as the starting material is not particularly limited. However, it must have at least one aromatic hydrogen and be able to undergo a condensation reaction with the acetal. Usable aromatic compounds are u. a. Carbocyclic compounds having the structure (1)
    (1) where
    Ri is hydrogen or an alkyl group having 1 to 4 carbon atoms, preferably 1 to 2 carbon atoms, R2 and R3 are independently hydrogen or an alkyl group having 1 to 4.
    Carbon atoms, preferably 1 to 2 carbon atoms, and Ri and R2 together may form a carboxyl ring system which may be saturated or unsaturated.
    Examples of these are benzene, toluene, m-, o- and p-xylene, cumene, ethylbenzene, pseudocumene, naphthalene and the like. A preferred aromatic compound is o-xylene.
    The acetal is not particularly limited, provided that it is capable of undergoing a condensation reaction with the aromatic compound. Usable acetals are u. a. Compounds with the structure (2)
    (2) where
    Ri and R5 are each independently hydrogen or an alkyl group of 1 to 6 carbon atoms, preferably hydrogen or an alkyl group of 1 to 2 hydrogen atoms, more preferably hydrogen, R6 and R7 are each independently an alkyl group of 1 to 6
    Carbon atoms, preferably having 1 to 2 carbon atoms, are.
    Preference is given to those acetals which are derived from the reaction of formaldehyde or an aldehyde having 1 to 6 carbon atoms and methanol or are derivable therefrom. A preferred acetal is DMM.
    The catalysts used in the process of this invention are perfluorinated sulfonic acid in polymeric form.
    Preferably, catalysts are used which are solid supported protic acids and in particular supported perfluorinated sulfonic acids in a polymeric form with silica as support material. Such catalysts are available, inter alia, under the trade names Nafion®, Aciplex® F, Femion®, Neosepta®, Fumion® F. A preferred catalyst is Nafion® SAC-13. Nafion® SAC-13 is porous silica particles on which Nafion® has been absorbed at a loading of about 13% by weight.
    The perfluorinated sulfonic acid in polymeric form preferably has the following structure (3):
    (3)
    The advantage of using a perfluorinated sulfonic acid in polymeric form in this process according to the invention is that the 1,1-diarylalkane with higher molar yield and, more importantly, with higher isomer selectivity than in a method using catalysts according to the prior Technology can be produced. Molar yield and isomer selectivity can be increased by using a solid or supported perfluorinated sulfonic acid in polymeric form as a catalyst. Furthermore, these solid or supported acids have the advantage that less fouling occurs and no secondary separation is required.
    The aromatic compound can serve as both a solvent and a reactant. Therefore, in the method according to the invention, the ratio of acetal to aromatic compound is preferably 0.04 to 25 wt .-%, in particular 4 to 10 wt .-% and most preferably 5 to 8 wt .-%, based on the aromatic compound. If the loading of the acetal in the aromatic compound is increased far beyond the mentioned ratio, this leads to an increase in polymer formation (yield loss and catalyst fouling). This ratio is a good balance between yield and throughput / productivity.
    The acetal can either be premixed with the aromatic compound or fed separately to the process. Preferably, the acetal with the. premixed aromatic compound and then fed to the reactor.
    The use of a further solvent in addition to the aromatic compound is not absolutely necessary in the process according to the invention. This has the advantage that no additional cleaning is required and the risk of undesired interaction is lower.
    The reaction can be carried out in a batch reactor, a continuous stirred tank, a catalyst bed reactor or a packed column. Preferably, the reaction is carried out in a packed catalyst or in a packed column because the catalyst must be changed at a time and it is desirable to minimize handling of the material. When using a continuous process, the reactor load is preferably in the range of 1 to 4 h'1, more preferably 1.5 to 3.5 h'1. In accordance with the present invention, the reactor load is defined as the reaction mixture in grams per hour and the catalyst used in grams.
    The process according to the invention can be carried out in a temperature range from 20 to 250.degree. C., preferably from 110 to 220.degree. C., particularly preferably from 160 to 180.degree.
    The process according to the invention can be carried out at ambient pressure or under pressure. Preferably, the reaction is carried out at a pressure of 1000 to 2000 kPa, particularly preferably 1250 to 1500 kPa, in order to ensure a single reaction phase in the reactor.
    In a preferred embodiment of the process of the invention, a tubular reactor is packed with a solid-supported perfluorosulfonic acid resin which is at the desired temperature, e.g. 110 to 220 ° C, is heated. A mixture of DMM, for example, in an amount of 0.04 to 25% by weight, in o-xylene is pumped at a reactor load of 0.01-200 h'1 into the tube reactor containing the catalyst. The process can be carried out at ambient pressure or under pressure. Preference is given to working under a pressure of 1250 to 1500 kPa in order to ensure a single reaction phase in the reactor.
    The reaction product can be worked up by distillation, preferably by fractional distillation. The excess of the aromatic compound removed from the reaction mixture can be used in another process.
    Higher isomer repeatability of the 1,1-diarylalkane is obtainable by fractional crystallization or zone purification.
    Examples
    The present invention will now be explained in detail by way of various examples. However, the embodiments of the invention should not be limited to the examples.
    example 1
    A tubular reactor (2.54 cm x 38.1 cm stainless steel) was charged with 18.01 grams of a solid supported perfluorosulfonic acid resin (Nafion® SAC-13).
    The catalyst bed was dried by heating to 150 ° C while purging with nitrogen overnight. The packed reactor was cooled to ambient temperature and provided at its outlet with a back pressure regulator set at 1379 kPa. The system was filled with o-xylene at a flow rate of 0.89 ml / min and the reactor bed was heated to 170 ° C. After the reactor bed reached the desired temperature, the feed of pure o-xylene was replaced with a 6 wt% solution of DMM in o-xylene and the flow rate maintained at 0.89 ml / min. Analysis of the product stream leaving the tube reactor revealed that the dixylylmethane (DXM) was produced in 79 mol% yield and with selectivity of about 75% for the isomer 3,3 ', 4,4'-tetramethyldiphenylmethane.
    Example 2
    The synthesis of DXM from DMM and o-xylene using a solid supported perfluorosulfonic acid resin (Nafion® SAC-13) was carried out using a similar equipment design as in Example 1.
    The catalyst-filled tube reactor was prepared by heating to 150 ° C with nitrogen purge overnight. The tube reactor was allowed to cool to room temperature. The pump was then turned on and the flow rate of the DMM / o-xylene mixture adjusted to 1.0 ml / min. The tube furnace temperature was set at 40 ° C and the reactor temperature was raised by 15 ° C every 0.5 to 2.0 hours. It has been found that the molar yield of DXM increases with temperature up to a temperature of 140 ° C. DMM was detected until reaching a reaction temperature of 180 ° C in the product stream. The best molar yield (85%), the best selectivity (70 to 75%) and the best DMM conversion (100%) were found at 180 ° C, a reactor loading of 2.9 h'1 (1.0 ml / min) and a DMM, concentration of 6 wt .-%.
    Example 3
    The synthesis of DXM from DMM and o-xylene using a solid-supported perfluorosulfonic acid resin was carried out using a similar equipment construction as in Example 1.
    The catalyst-filled tube reactor was prepared by heating to 150 ° C with nitrogen purge overnight. The tube reactor was allowed to cool to room temperature. The pump was then turned on and the flow rate of the DMM / o-xylene mixture adjusted to 1.0 ml / min. The tube furnace temperature was adjusted to 40 ° C, and the reactor temperature was increased until the reaction temperature reached 160 °, 170 ° or 180 ° C and then held at this temperature for a period of 8 to 10 hours, at regular intervals a sample of the Product stream was taken. The analysis revealed that the molar yield of DXM was constant at 60%. It was also observed that the isomer selectivity over this range was consistently 70%.
    Comparative Example 1
    The synthesis of DXM from DMM and o-xylene using various acid catalysts, such as activated weakly acidic alumina, activated neutral alumina and alumina, respectively, with a loading of 1% H3PO4, was carried out using a similar equipment setup as in Example 1.
    After heating the reactor to 100 ° C, a flow of the 6 wt% solution of DMM in o-xylene was set at 1.0 ml / min. Samples were taken every 30 minutes and the tube furnace temperature was increased by 20 ° C every hour. At temperatures above 140 ° C, the evolution of gas from the reactor column was observed. Upon reaching a reactor temperature of 360 ° C, the reaction was completed.
    Evaluation of these alternative catalysts did not produce DXM. However, these experiments show that the upper temperature that can be used with DMM is 180 to 200 ° C because of its decomposition. Degradation of DMM by GC analysis is shown in Table 1. The similarity of these data indicates that this decomposition of the DMM is independent of the catalyst.
    Table 1
    Comparative Example 2
    The synthesis of DXM from DMM and o-xylene using a sulfonic acid resin (Amberlyst® XN 1010 - high surface area sulfonated styrene-divinylbenzene hydrogen form) was carried out using a similar equipment construction as in Example 1.
    The flow rate of the tube reactor was set at 1.0 ml / min and the furnace temperature was set at 60 ° C. Samples were taken every 30 minutes and the tube furnace temperature was increased by 20 ° C every 0.5 to 2.0 hours. The product stream leaving the tube reactor turned yellow at a reactor temperature of 110 ° C. At temperatures above 140 ° C, the evolution of gas from the reactor column was observed, and upon reaching a reactor temperature of 150 ° C, the experiment was terminated. As can be seen from Table 2, the best result with this catalyst was a molar yield of 39% with a selectivity of 60%. This comparative example demonstrates that the sulfonic acid resin provides unsatisfactory yields of DXM in a once-through continuous flow system.
    Comparative Example 3
    The synthesis of DXM from DMM and o-xylene using a synthetic acid aluminosilicate (Catalyst H Beta 25 zeolites) was carried out using a similar equipment construction as in Comparative Example 2.
    The results of this experiment are shown in Table 2.
    Table 2

    1) Decreased over time due to catalyst poisoning.
    means that under the stated conditions no measurement was made.
    "0" means that a measurement was taken but the product, if any, was below the detection limit of the analytical method.
    Examples 4-5 and Comparative Examples 4-7
    A tube reactor (2.54 cm x 38.1 cm stainless steel) was charged with 18.01 g of the catalyst. The catalyst bed was dried by heating to 150 ° C while purging with nitrogen overnight. The packed reactor was cooled to ambient temperature and provided at its outlet with a back pressure regulator set at 1379 kPa. The system was charged with o-xylene at a flow rate of 1 ml / min, and the reactor bed was heated to 170 ° C. After the reactor bed reached the desired temperature, the feed of pure o-xylene was replaced with a 6 wt% solution of DMM in o-xylene and the flow rate was adjusted to 1 ml / min. The results of this experiment are shown in Table 3.
    Table 3:

    Catalyst can be regenerated by heating to 500 DC. 3) KataJysato quality decreased at 150 ° C
    The results of these examples and comparative examples show that the molar yield, the. Selectivity and the conversion of DMM using a Feststoffgeträgerten Perfluorsulfonsäureharzes have the highest values.
    权利要求:
    Claims (7)
    [1]
    1. A process for the preparation of 1,1-diarylalkanes characterized in that an aromatic compound having at least one aromatic hydrogen is reacted with an acetal in the presence of a perfluorinated sulfonic acid in polymeric form as a catalyst.
    [2]
    2. The method according to claim 1, characterized in that a solid or supported acid is used as a catalyst.
    [3]
    3. The method according to claim 2, characterized in that a supported perfluorinated sulfonic acid is used in polymeric form with silica as a support material as a catalyst.
    [4]
    4. The method according to at least one of claims 1 to 3, characterized in that the ratio of acetal to aromatic compound 4 to 10 wt .-% based on the aromatic compound.
    [5]
    5. The method according to claim 4, characterized in that the ratio of acetal to the aromatic compound 5 to 8 wt .-% based on the aromatic compound.
    [6]
    6. The method according to at least one of claims 1 to 5, characterized in that the reaction is carried out at a pressure of 1000 to 2000 kPa.
    [7]
    7. The method according to claim 6, characterized in that the reaction is carried out at one of 1250 to 1500 kPa.
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    法律状态:
    优先权:
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