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  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
  • B01J19/12—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electromagnetic waves
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
  • B01J8/18—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
  • B01J8/24—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique
  • B01J8/42—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with fluidised bed subjected to electric current or to radiations this sub-group includes the fluidised bed subjected to electric or magnetic fields
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  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
  • C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
  • C07C205/57—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
  • C07C205/59—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms
  • C07C205/60—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms in ortho-position to the carboxyl group, e.g. nitro-salicylic acids
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  • C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
  • C07C209/30—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds
  • C07C209/32—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds by reduction of nitro groups
  • C07C209/36—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds by reduction of nitro groups by reduction of nitro groups bound to carbon atoms of six-membered aromatic rings in presence of hydrogen-containing gases and a catalyst
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  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
  • C07C37/01—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis
  • C07C37/055—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis the substituted group being bound to oxygen, e.g. ether group
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
  • C07C41/01—Preparation of ethers
  • C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
  • C07C41/30—Preparation of ethers by reactions not forming ether-oxygen bonds by increasing the number of carbon atoms, e.g. by oligomerisation
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  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
  • C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
  • C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
  • C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
  • C07C45/69—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to carbon-to-carbon double or triple bonds
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C67/00—Preparation of carboxylic acid esters
  • C07C67/03—Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C67/00—Preparation of carboxylic acid esters
  • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
  • C07C67/303—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by hydrogenation of unsaturated carbon-to-carbon bonds
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
  • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
  • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
  • C07D295/06—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by halogen atoms or nitro radicals
  • C07D295/073—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by halogen atoms or nitro radicals with the ring nitrogen atoms and the substituents separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
• • H—ELECTRICITY
  • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
  • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
  • H05B6/00—Heating by electric, magnetic or electromagnetic fields
  • H05B6/02—Induction heating
  • H05B6/10—Induction heating apparatus, other than furnaces, for specific applications
  • H05B6/105—Induction heating apparatus, other than furnaces, for specific applications using a susceptor
  • H05B6/106—Induction heating apparatus, other than furnaces, for specific applications using a susceptor in the form of fillings
• • H—ELECTRICITY
  • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
  • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
  • H05B6/00—Heating by electric, magnetic or electromagnetic fields
  • H05B6/02—Induction heating
  • H05B6/10—Induction heating apparatus, other than furnaces, for specific applications
  • H05B6/105—Induction heating apparatus, other than furnaces, for specific applications using a susceptor
  • H05B6/108—Induction heating apparatus, other than furnaces, for specific applications using a susceptor for heating a fluid
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
  • B01J2208/00008—Controlling the process
  • B01J2208/00017—Controlling the temperature
  • B01J2208/00327—Controlling the temperature by direct heat exchange
  • B01J2208/00336—Controlling the temperature by direct heat exchange adding a temperature modifying medium to the reactants
  • B01J2208/0038—Solids
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
  • B01J2208/00008—Controlling the process
  • B01J2208/00017—Controlling the temperature
  • B01J2208/00433—Controlling the temperature using electromagnetic heating
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
  • B01J2208/00008—Controlling the process
  • B01J2208/00017—Controlling the temperature
  • B01J2208/00513—Controlling the temperature using inert heat absorbing solids in the bed
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/00049—Controlling or regulating processes
  • B01J2219/00051—Controlling the temperature
  • B01J2219/00139—Controlling the temperature using electromagnetic heating

Definitions

• the present invention is in the field of chemical synthesis and relates to a process for carrying out a chemical reaction with the help of an inductively heated heating medium.
• the present invention provides a process, in which the reaction medium is heated by bringing it into contact with a heating medium that can be heated by electromagnetic induction and which is heated “from the exterior” by electromagnetic induction with the aid of an inductor.
• inductive heating has been used for some time in industry. The most frequent applications are melting, curing, sintering and the heat treatment of alloys. However, processes such as gluing, shrinking or bonding of components are also known applications of this heating technology.
• the magnetic particles can be heated in a high frequency magnetic alternating field to temperatures of preferably 40 to 120° C. that are relevant for analysis, diagnostics and therapy.” Furthermore, this document treats the technical design of rinsing systems and high frequency generators, which can be used in this process. The cited document thus describes the use of inductively heatable particles for the analysis of complex biological systems or biomolecules.
• U.S. Pat. No. 5,110,996 describes the preparation of vinylidene fluoride by the gaseous phase reaction of dichlorodifluoromethane with methane in a heated reactor.
• the reactor was filled with a non-metallic filler.
• a metallic hull that is heated from the exterior by electromagnetic induction surrounds the reaction chamber that contains this filler.
• the reaction chamber itself is therefore heated from the exterior, whereby the filler is likewise heated over time by radiating heat and/or thermal conductivity.
• a direct heating of the filler circulated by the reactants does not occur if this filler is electrically conductive, as the metallic reactor wall shields the electromagnetic fields from the induction coil.
• WO 95/21126 discloses a gas phase process for preparing hydrogen cyanide from ammonia and a hydrocarbon with the aid of a metallic catalyst.
• the catalyst is inside the reaction chamber so that reactants circulate round the catalyst. It is heated from the exterior by electromagnetic induction with a frequency of 0.5 to 30 MHz, i.e. with a high frequency alternating field.
• this document cites the previously cited document U.S. Pat. No. 5,110,996 with the remark that normally, inductive heating is carried out in the frequency range from about 0.1 to 0.2 MHz.
• this indication is not comprised in the cited U.S. Pat. No. 5,110,996, and it is unclear what it refers to.
• WO 00/38831 is concerned with controlled adsorption and desorption processes, wherein the temperature of the adsorber material is controlled by electromagnetic induction.
• the subject matter of the present invention is a process for carrying out a chemical reaction for producing a target compound by heating a reaction medium comprising at least one first reactant in a reactor, whereby a chemical bond within the first reactant or between the first and a second reactant is formed or modified, wherein the reaction medium is brought into contact with a solid heating medium that can be heated by electromagnetic induction and that is inside the reactor and is surrounded by the reaction medium, and said heating medium is heated by electromagnetic induction with the aid of an inductor, wherein the target compound is formed from the first reactant or from the first and a second reactant and wherein said target compound is separated from the heating medium.
• the chemical reaction takes place by heating a reaction medium that comprises at least one first reactant.
• the reaction medium for example a liquid
• the reaction medium can therefore consist of one reactant.
• a reactant can be dissolved or dispersed in the reaction medium, wherein the reaction medium can itself be inert or can represent for its part a reactant. Or one, two or more reactants are dissolved or dispersed in a reaction medium that is itself not changed by the chemical reaction.
• reaction medium can consist of a single reactant or comprise it, wherein reactant molecules react with one another or wherein a modification of the chemical bonding system can occur in the individual molecules of the reactant itself.
• the reactant is chemically modified in both cases. In the general case, however, two or more reactants participate with one another in reaction, wherein chemical bonds within and/or between the individual reactants are rearranged or formed.
• the solid heating medium is surrounded by the reaction medium.
• This can mean that the solid heating medium, apart from possible peripheral zones, is present within the reaction medium, e.g. when the heating medium is present in the form of particles, filings, wires, gauze, wool, packing materials etc.
• the reaction medium flows through the heating medium through a plurality of cavities in the heating medium, when for example the latter consists of one or more membranes, a bundle of pipes, a rolled up metal foil, frits, porous packing materials or from a foam.
• the heating medium is also essentially surrounded by the reaction medium, as the majority of its surface (90% or more) remains in contact with the reaction medium.
• a reactor whose external wall is heated by electromagnetic induction (such as for example that cited in the document U.S. Pat. No. 5,110,996), where only the inner reactor surface comes into contact with the reaction medium.
• the wall of the reactor is made of a material that neither shields nor absorbs the electromagnetic alternating field produced by the inductor and therefore is itself not heated up. Consequently, metals are unsuitable.
• it can consist of plastic, glass or ceramics (such as for example silicon carbide or silicon nitride). The last mentioned is particularly suitable for reactions at high temperatures (500-600° C.) and/or under pressure.
• the above-described method has the advantage that the thermal energy for carrying out the chemical reaction is not brought into the reaction medium through surfaces such as for example the reactor walls, heating coils, heat exchange plates or the like, but rather is produced directly in the volume of the reactor.
• the ratio of heated surface to volume of the reaction medium can, in this case, be considerably greater than for a heating through heat transfer surfaces, as is also the case, for example, cited in DE 10 2005 051637 in the introduction.
• the degree of efficiency of electrical current to thermal output is improved.
• the target compound After the target compound is formed it is separated from the heating medium.
• the target compound In the best case the target compound is isolated in pure form, i.e. free of solvent and with no more than the usual impurities.
• the target compound can also be separated from the heating medium in a mixture with reactants or as a solution in the reaction mixture and then be isolated by further working up or be transferred into another solvent, as is desired. The process is therefore suitable for the preparative manufacture of the target compound in order to be able to use these in a further step.
• a chemical reaction is indeed likewise initiated by electromagnetic induction of a heating medium, but the reaction does not serve to prepare a target compound that is separated from the heating medium after the end of the reaction.
• An example of this is the curing of resin systems, wherein the curing reaction is initiated on particles that are dispersed in the resin system and which are heated by electromagnetic induction. In such a case the particles remain in the cured resin system and no defined target compound is isolated.
• an adhesive compound is unglued again by the inductively heated particles that are present in the adhesive matrix.
• a chemical reaction can indeed occur in this case, but no target compound is isolated.
• the heating medium consists of an electrically conductive material that is heated by the action of an alternating electrical field. It is preferably selected from materials that possess a very high surface to volume ratio.
• the heating medium can be selected in each case from electrically conductive filings, wires, meshes, wool, membranes, porous frits, pipe bundles (of three or more pipes), rolled up metal foils, foams, packing materials such as for example granules or pellets, Raschig rings and particularly particles that preferably have an average diameter of not more than 1 mm.
• mixed metallic elements can be employed as the heating medium, as are used for static mixers.
• the heating medium is electrically conductive, for example metallic (wherein it can be diamagnetic) or it exhibits enhanced interaction towards diamagnetism with a magnetic field and in particular is ferromagnetic, ferrimagnetic, paramagnetic or superparamagnetic.
• the heating medium is of an organic or inorganic nature or whether it contains both inorganic as well as organic components.
• the heating medium is selected from particles of electrically conductive and/or magnetizable solids, wherein the mean particle size of the particles is from 1 to 1000, especially from 10 to 500 nm.
• the mean particle size and when necessary also the particle size distribution can be determined for example by light scattering.
• Magnetic particles are preferably selected, for example ferromagnetic or superparamagnetic particles, which exhibit the lowest possible remanence or residual magnetism. This has the advantage that the particles do not adhere to each other.
• the magnetic particles can be in the form of “ferrofluids”, i.e. liquids, in which nanoscale ferromagnetic particles are dispersed. The liquid phase of the ferrofluid can then serve as the reaction medium.
• Magnetizable particles in particular ferromagnetic particles, which exhibit the desired properties, are known from the prior art and are commercially available.
• the commercially available ferrofluids may be cited.
• Examples for the manufacture of magnetic nano-particles, which can be used in the context of the inventive process, can be found in the article by Lu, Salabas and Schüth: “Magnetician nano-Pelle: Synthese, Stabilmaschine,temperaturalmaschine and für”, Angew. Chem. 2007, 119, pp. 1242 to 1266.
• Suitable nano-particles with different compositions and phases are known.
• the following examples may be cited: pure metals such as Fe, Co and Ni, oxides such as Fe 3 O 4 and gamma-Fe 2 O 3 , spinel type ferromagnets such as MgFe 2 O 4 , MnFe 2 O 4 and CoFe 2 O 4 as well as alloys such as CoPt 3 and FePt.
• the magnetic nano-particles can be of a homogeneous structure or can possess a core-shell structure. In the latter case the core and shell can consist of different ferromagnetic or even antiferromagnetic materials.
• a magnetizable core that can be for example ferromagnetic, antiferromagnetic, paramagnetic or superparamagnetic, is surrounded by a non-magnetic material.
• An organic polymer for example, can represent this material.
• the shell consists of an inorganic material such as for example silica or SiO 2 .
• a coating of this type can prevent a chemical interaction between the reaction medium or the reactants with the material of the magnetic particle itself.
• the shell material can be surface modified, without the material of the magnetizable core interacting with the functionalizing entity.
• a plurality of particles of the core material can be enclosed together into a shell of this type.
• Nano-scale particles of superparamagnetic substances for example can be employed as the heating medium and are selected from aluminum, cobalt, iron, nickel or their alloys, metal oxides of the type n-maghemite (gamma-Fe 2 O 3 ), n-magnetite (Fe 3 O 4 ) or ferrites of the type MeFe 2 O 4 , wherein Me is a divalent metal selected from manganese, copper, zinc, cobalt, nickel, magnesium, calcium or cadmium.
• Me is a divalent metal selected from manganese, copper, zinc, cobalt, nickel, magnesium, calcium or cadmium.
• An exemplary suitable material is available from Evonik (formally Degussa) under the name MagSilica®.
• MagSilica® An exemplary suitable material is available from Evonik (formally Degussa) under the name MagSilica®.
• iron oxide particles having a size between 5 and 30 nm are embedded in an amorphous silica matrix.
• Such iron oxide-silicon dioxide composite particles which are described in more detail in the German patent application DE 101 40 089, are particularly suitable.
• These particles can comprise superparamagnetic iron oxide domains with a diameter of 3 to 20 nm. This is understood to mean superparamagnetic regions that are spatially separated from one another.
• the iron oxide can be present in these domains in a single modification or in various modifications.
• a particularly preferred superparamagnetic iron oxide domain is gamma-Fe 2 O 3 , Fe 3 O 4 and mixtures thereof.
• the content of the superparamagnetic iron oxide domains of these particles can be between 1 and 99.6 wt. %.
• the individual domains are separated from one another and/or surrounded by a non-magnetizable silicon dioxide matrix.
• the region containing a content of the superparamagnetic iron oxide domains is preferably >30 wt. %, particularly preferably >50 wt. %.
• the achievable magnetic effect of the inventive particle also increases with the content of the superparamagnetic regions.
• the silicon dioxide matrix also stabilizes the oxidation level of the domain in addition to separating the spatial separation of the superparamagnetic iron oxide domains.
• magnetite is stabilized as the superparamagnetic iron oxide phase by a silicon dioxide matrix.
• nano-scale ferrites such as those known for example from WO 03/054102 can be employed as the heating medium.
• These ferrites possess the composition (M a 1-x-y M b x Fe II y )Fe III 2 O 4 , in which
• M a is selected from Mn, Co, Ni, Mg, Ca, Cu, Zn, Y and V
• M b is selected from Zn and Cd
• x stands for 0.05 to 0.95, preferably 0.01 to 0.8
• y stands for 0 to 0.95 and the sum of x and y is maximum 1.
• the particles that can be heated by electromagnetic induction can represent the heating medium without any additional additives. However, it is also possible to mix the particles that can be heated by electromagnetic induction with other particles that cannot be heated by electromagnetic induction. Sand for example can be used. Accordingly, the inductively heatable particles can be diluted with non-inductively heatable particles. This allows an improved temperature control. In another embodiment, the inductively heatable particles can be admixed with non-inductively heatable particles that have catalytic properties for the chemical reaction to be carried out or that participate in other ways in the chemical reaction. These particles are then not directly heated by electromagnetic induction, but rather indirectly, in that they are heated by contact with the heatable particles or by heat transfer from the reaction medium.
• nano-scale electromagnetically inductively heatable particles are blended with coarser non-inductively heatable particles, then this can lead to a decreased packing density of the heating medium.
• this can result in a desired reduction of the pressure drop in the flow-through reactor.
• the solid heating medium can be surface-coated with a substance that is catalytically active for the desired chemical reaction.
• a substance that is catalytically active for the desired chemical reaction can be organic molecules or biomolecules having an enzymatic action. In this case care should be taken to ensure that the heating medium is not heated too strongly to cause these molecules to lose their enzymatic action.
• the inductively heatable heating medium can be coated with metal atoms or metallic compounds, whose catalytic activity is known.
• metal atoms or metallic compounds can be of the lanthanide series, especially Sm or Ce, Fe, Co, Ni or precious metals, preferably platinum metals and especially Pt or Pd.
• Particles that comprise magnetizable domains in a silicon dioxide matrix or silica matrix are particularly suitable for coating with catalytically active atoms or compounds.
• the silicon dioxide shell carries, as is described in more detail in WO 03/042315, reactive OH groups, whose reactivity can be exploited in order to fix the catalytically active substance to the particle surface.
• the chemical reaction can be carried out in a continuous or batch manner. If the reaction is carried out in a batch mode, then the reactive medium and the inductively heated solid heating medium preferably move relative to one another during the reaction. When using a particulate heating medium this can be effected in particular by stirring the reaction mixture with the heating medium or by swirling the heating medium in the reaction medium. If for example meshes or wool are used in a filiform shaped heating medium, then the reaction vessel that contains the reaction medium and the heating medium can be shaken.
• a preferred embodiment of a batch mode reaction consists in the reaction medium being present together with particles of the heating medium in a reaction vessel, and is moved with the help of a moving element located in the reaction medium, wherein the moving element is arranged as the inductor, by which the particles of the heating medium are heated by electromagnetic induction. Consequently, in this embodiment the inductor is found inside the reaction medium.
• the moving element can be designed for example as a stirrer or as a plunger that moves back and forth.
• Provision for externally cooling the reactor during the chemical reaction can also be made. This is possible in particular for batch modes if, as described above, the inductor is immersed in the reaction medium. The supply of the electromagnetic alternating field into the reactor is then not impeded by the cooling apparatus.
• the reactor can be cooled from inside by cooling coils or heat exchangers or preferably from outside.
• a coolant for example whose temperature is below 0° C.
• Exemplary coolants of this type are ice-table salt mixtures, methanol/dry ice or liquid nitrogen.
• the cooling creates a temperature gradient between the reactor wall and the inductively heated heating medium. This is particularly pronounced when a coolant with a temperature significantly below 0° C. is used, for example methanol/dry ice or liquid nitrogen.
• the reaction medium that is heated by the inductively heated heating medium is then externally cooled down again. In this case the chemical reaction of the reactants then only occurs when it is in contact with the heating medium or is at least in its direct proximity.
• reaction medium Due to the relative movement of the reaction medium to the heating medium, products formed during the reaction rapidly reach cooler regions of the reaction medium, such that their thermal subsequent reaction is inhibited. In this way, a desired reaction path can be kinetically selected when a plurality of possible reaction paths of the reactant(s) exist.
• the chemical reaction is carried out continuously in a flow-through reactor that is at least partially filled with the solid heating medium and thereby possesses at least one heating zone that can be heated by electromagnetic induction, wherein the reaction medium flows continuously through the flow-through reactor and wherein the inductor is located outside the reactor.
• the reaction medium flows round the heating medium, e.g. when this is in the form of particles, filings, wires, meshes, wool, packing materials etc.
• the reaction medium flows through the heating medium through a plurality of cavities in the heating medium, when this consists for example of one or a plurality of membranes, fits, porous packing materials or a foam.
• the flow-through reactor is preferably designed as a tubular reactor.
• the inductor can totally or at least partially surround the reactor.
• the electromagnetic alternating field generated by the inductor is then fed from all sides or at least from a plurality of places into the reactor.
• Continuous is hereby understood to mean as usual a reaction mode, in which the reaction medium flows through the reactor in at least such a period of time that a total volume of reaction medium that is large in comparison with the internal volume of the reactor itself has flowed through the reactor, before the flow of reaction medium is discontinued.
• “Large” in this context means: “at least twice as large”.
• a continuously operated reaction of this type also has a beginning and an end.
• the reactor In this continuous process in a flow-through reactor it is possible for the reactor to have a plurality of heating zones.
• the different heating zones can be differently heated for example. This can be the result of arranging different heating media in the flow-through reactor or due to differently mounted inductors along the reactor.
• the use of at least two heating zones constitutes a particular embodiment, in that the flow-through reactor possesses a first and a second heating zone, wherein the first heating zone in the flow direction of the reaction medium does not comprise a heating medium loaded with a catalytically active substance, whereas the second heating zone in the flow direction of the reaction medium does comprise a heating medium loaded with a catalytically active substance.
• the opposite arrangement is chosen for the catalytically and non-catalytically active heating medium. This allows an additional non-catalytically initiated reaction step to be carried out prior to or after a catalytically active reaction step.
• the solvent or the reaction medium can also be initially preheated in a conventional manner prior to its contacting the heating medium in the reaction.
• a cooling zone for example in the form of a cooling jacket around the reactor, can be provided after the (last) heating zone.
• the reaction medium can be brought into contact with an absorbing substance that removes by-products or impurities from the reaction medium.
• an absorbing substance that removes by-products or impurities from the reaction medium.
• it can be a molecular sieve, through which flows the reaction medium after having left the heating zones. In this way the product can be purified immediately after its production.
• the product yield can optionally be increased by at least partially recycling the reaction medium that has flowed through the solid heating medium back through the solid heating medium again.
• the impurities, by-products or even the desired major product can be removed from the reaction medium after each passage through the solid heating medium.
• the various known separation methods are suitable for this, for example absorption on an absorbing substance, separation through a membrane process, precipitation by cooling or separation by distillation. This ultimately enables a complete conversion of the reactant(s) to be achieved. This is also true in cases where without separating the reaction product the chemical reaction only proceeds to an equilibrium state.
• the required total contact time of the reaction medium with the inductively heated heating medium needs to be chosen as a function of the kinetics of each chemical reaction.
• the slower the desired chemical reaction the longer the contact time. This has to be empirically adjusted for each individual case.
• the reaction medium preferably flows once or a plurality of times through the flow-though reactor with a speed such that the total contact time of the reaction medium with the inductively heated heating medium is in the range of one second to 2 hours prior to separating the target product. Shorter contact times are conceivable but more difficult to control. Longer contact times can be required for particularly slow chemical reactions, but increasingly worsen the economics of the process.
• the reactor can be designed as a pressure reactor and the chemical reaction is carried out at a pressure greater than atmospheric pressure, preferably under at least 1.5 bar. It is well known that the product yield can be increased in this way when the product formation (formation of the target compound) is associated with a volume reduction. For two or more possible reactions, the formation of that particular product can be preferred that results in the greatest reduction in volume.
• the inventive process is preferably carried out in such a way that the reaction medium in the reactor is in liquid form under the set reaction conditions (particularly temperature and pressure). This generally makes possible, based on the reactor volume, better volume/yields over time than for gas phase reactions.
• the nature of the heating medium and the design of the inductor are matched to each other in such a way to permit the reaction medium to be heated up.
• a critical variable for this is firstly the rated power of the inductor in watts as well as the frequency of the alternating field generated by the inductor.
• the greater the mass of the heating medium to be inductively heated the higher will be the chosen power.
• the achievable power is limited primarily by the ability to cool the generator required for supplying the inductor.
• Particularly suitable inductors generate an alternating field with a frequency in the range of about 1 to about 100 kHz, preferably from 10 to 80 kHz and particularly preferably from about 10 to about 30 kHz.
• Inductors of this type together with the associated generators are commercially available, for example from IFF GmbH in Ismaning (Germany).
• the inductive heating is preferably carried out with an alternating field in the medium frequency range.
• This has the advantage, when compared with an excitation with higher frequencies, for example with those in the high frequency range (frequencies above 0.5, especially above 1 MHz), that the energy input into the heating medium can be better controlled.
• the reaction medium is in liquid form under the reaction conditions. Consequently, in the context of the present invention the reaction medium is preferably in liquid form and inductors are employed that generate an alternating field in the abovementioned medium frequency range. This permits an economic and well controllable reaction process.
• the heating medium is ferromagnetic and exhibits a Curie temperature in the range of about 40° C. to about 250° C., and is selected such that the Curie temperature does not differ by more than 20° C., preferably by not more than 10° C. from the selected reaction temperature.
• the heating medium can be heated by electromagnetic induction only up to its Curie temperature; it will not be heated any further above this temperature by the electromagnetic alternating field. Even with a malfunction of the inductor, the temperature of the reaction medium is prevented from any unintentional increase to a value significantly above the Curie temperature of the heating medium. Should the temperature of the heating medium fall below its Curie temperature then it will again be heated by electromagnetic induction. This leads to a self-regulation of the temperature of the heating medium in the region of the Curie temperature.
• the inventive process is particularly suitable for carrying out thermally induced reactions.
• reaction conditions such as for example pH
• educts are chosen that could destroy the heating medium.
• chemical reactions can be carried out in which at least one chemical bond between two carbon atoms or between a carbon atom and an atom X is formed, cleaved or rearranged, wherein X is selected from: H, B, O, N, S, P, Si, Ge, Sn, Pb, As, Sb, Bi and halogens.
• the reaction can also involve a rearrangement of chemical bonds, such as occurs for example in cycloadditions and Diels-Alder reactions.
• the thermally induced reaction can correspond to at least one of the following reaction types: oxidation, reduction (including hydrogenation), fragmentation, addition to a double or triple bond (incl. cycloaddition and Diels-Alder reactions), substitution (SN 1 or SN 2 , radical), especially aromatic substitution, elimination, rearrangement, cross coupling, metathetical reactions, formation of heterocycles, ether formation, ester formation or transesterification, amine or amide formation, urethane formation, pericyclic reactions, Michael addition, condensation, polymerization (radical, anionic, cationic), polymer grafting.
• reaction types oxidation, reduction (including hydrogenation), fragmentation, addition to a double or triple bond (incl. cycloaddition and Diels-Alder reactions), substitution (SN 1 or SN 2 , radical), especially aromatic substitution, elimination, rearrangement, cross coupling, metathetical reactions, formation of heterocycles, ether formation, ester formation or transesterification, amine or
• suitable reducing agents or hydrogen sources are for example: cycloalkenes such as cyclohexene, alcohols such as ethanol, inorganic hydrogenation reagents such as sodium borohydride or sodium aluminum hydride.
• Fats or oils for example can be fragmented. This can occur in solution, but also in the substance in the absence of solvent. In the latter case the fat or oil as such represents the whole reaction medium.
• the invention was tested on a laboratory scale. Glass tubes (10 cm long) and of varying inner and outer diameters were used as the tubular reactors. The tubes were provided with screw connections on both ends so as to be able to attach the HPLC and suitable tubing.
• the diameter of the gap for receiving the tubular reactor was 12 mm.
• the inductor was operated with a frequency of 25 kHz.
• thermocouple The induced temperature was measured with a thermocouple and an infrared thermometer.
• the thermocouple was mounted directly behind the reactor in the fluid so as to permit an accurate as possible measurement.
• a laser infrared thermometer with close focus optics was used for the second temperature measurement.
• the measurement point had a diameter of 1 mm.
• the emission factor of the material is an important constant for an infrared measurement. It is a measure of the heat emission. An emission factor of 0.85 was used and corresponds to that of an average glass.
• Bayferrox® 318 M synthetic alpha-Fe 3 O 4 from Harald Scholz & Co. GmbH
• the reactor was filled with 3.3 g of the cited material in order to obtain the desired heating by the inductor for the reactions.
• the heating of rolled copper foil by electromagnetic induction was examined: The foil was heated at a frequency of 20 kHz and a PWM of only 175 ⁇ after less than 10 minutes to >160° C.
• the heating medium for the following experiments was Magsilica 58/85 from Evonik (formerly Degussa) and was optionally surface modified according to the following process.
• MagSilica 50/85® (15.0 g) was heated under reflux for 2 h in bidistilled H2O (150 mL) and then dried under high vacuum.
• the solid was suspended in toluene (180 mL) and shaken with (p-chloromethyl)phenyltrimethoxysilane (15 mL, 68.1 mmol) for 26 h.
• the reaction mixture was heated under reflux for 3 h. After cooling the solid was centrifuged and washed with toluene (2 ⁇ 40 mL). After drying under high vacuum 12.1 g of 14 were obtained as a black, magnetic powder.
• MagSilica 50/85® (6.0 g) was dried at 200° C. for 6 h under high vacuum and then suspended in abs. toluene (150 mL) in an inert gas atmosphere. 3-Aminopropyltrimethoxysilane (4.5 mL, 25.3 mmol) in abs. toluene (10 mL) was added. The reaction mixture was shaken for 16 h and centrifuged. The solid was washed with abs. toluene (2 ⁇ 40 mL) and aqueous toluene (1 ⁇ 40 mL) and then dried under high vacuum. 5.3 g of 12 were obtained as a black, magnetic powder.
• MagSilica 50/85® (2.0 g) was suspended in EtOH and stirred with a solution of palladium nitrate dihydrate (84 mg, 0.32 mmol) in EtOH (10 mL) at 50° C. for 30 min. The reaction mixture was concentrated under vacuum until dry. After drying under vacuum, 1.92 g of 8 were obtained as a black, magnetic powder. The catalyst loading was 11.3 ⁇ 10 ⁇ 5 mmol Pd/mg catalyst.
• MagSilica 50/85® (3.0 g) was heated under reflux for 2 h in bidistilled H2O (50 mL) and then dried under high vacuum.
• the black solid in dodecane (18 mL) was treated with DVB (0.41 g, 5.3 m %), VBC (7.11 g, 94.7 m %) and AIBN (37.5 mg, 0.5 m %) and stirred with a KPG-stirrer at 70° C. for 16 h.
• the resulting black suspension was purified in a soxhlet extraction unit for 13 h with chloroform.
• the product was separated from the residual polymer and dried under high vacuum. 4.4 g of 63 were obtained as a black-greenish, magnetic powder.
• 63 (4.4 g) was suspended in a toluene solution (350 mL) saturated with trimethylamine and shaken for 93 h. The solid was centrifuged and washed with toluene (3 ⁇ 40 mL). After drying under high vacuum a black-greenish, magnetic powder was obtained. 4.1 g of 63 were obtained.
• the Pd/C catalyst (palladium on active carbon) was employed in a mixture with MagSilica®. Cyclohexene essentially served as the reducing agent (hydrogen source).

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