EP3052459A1 - Pd on ceria catalytic system for selective hydrogenations of triple bonds - Google Patents

Pd on ceria catalytic system for selective hydrogenations of triple bonds

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Publication number
EP3052459A1
EP3052459A1 EP14777090.3A EP14777090A EP3052459A1 EP 3052459 A1 EP3052459 A1 EP 3052459A1 EP 14777090 A EP14777090 A EP 14777090A EP 3052459 A1 EP3052459 A1 EP 3052459A1
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EP
European Patent Office
Prior art keywords
catalytic system
present
catalytic
carrier material
relates
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP14777090.3A
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German (de)
French (fr)
Inventor
Giancarlo Cravotto
Werner Bonrath
Jonathan Alan Medlock
Emily BORETTO
Zihilin WU
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DSM IP Assets BV
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DSM IP Assets BV
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Priority to EP14777090.3A priority Critical patent/EP3052459A1/en
Publication of EP3052459A1 publication Critical patent/EP3052459A1/en
Ceased legal-status Critical Current

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    • 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
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/44—Palladium
    • 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
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
    • B01J21/04—Alumina
    • 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
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56—Platinum group metals
    • B01J23/63—Platinum group metals with rare earths or actinides
    • 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
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/78—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with alkali- or alkaline earth metals
    • 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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/0201—Impregnation
    • 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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/0201—Impregnation
    • B01J37/0203—Impregnation the impregnation liquid containing organic compounds
    • 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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/0201—Impregnation
    • B01J37/0211—Impregnation using a colloidal suspension
    • 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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/34—Irradiation by, or application of, electric, magnetic or wave energy, e.g. ultrasonic waves ; Ionic sputtering; Flame or plasma spraying; Particle radiation
    • B01J37/341—Irradiation by, or application of, electric, magnetic or wave energy, e.g. ultrasonic waves ; Ionic sputtering; Flame or plasma spraying; Particle radiation making use of electric or magnetic fields, wave energy or particle radiation
    • B01J37/343—Irradiation by, or application of, electric, magnetic or wave energy, e.g. ultrasonic waves ; Ionic sputtering; Flame or plasma spraying; Particle radiation making use of electric or magnetic fields, wave energy or particle radiation of ultrasonic wave energy
    • 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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/34—Irradiation by, or application of, electric, magnetic or wave energy, e.g. ultrasonic waves ; Ionic sputtering; Flame or plasma spraying; Particle radiation
    • B01J37/341—Irradiation by, or application of, electric, magnetic or wave energy, e.g. ultrasonic waves ; Ionic sputtering; Flame or plasma spraying; Particle radiation making use of electric or magnetic fields, wave energy or particle radiation
    • B01J37/344—Irradiation by, or application of, electric, magnetic or wave energy, e.g. ultrasonic waves ; Ionic sputtering; Flame or plasma spraying; Particle radiation making use of electric or magnetic fields, wave energy or particle radiation of electromagnetic wave energy
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/17—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/02—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
    • C07C5/08—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of carbon-to-carbon triple bonds
    • C07C5/09—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of carbon-to-carbon triple bonds to carbon-to-carbon double bonds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/10—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of rare earths
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
    • C07C2523/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
    • C07C2523/44—Palladium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/14—Phosphorus; Compounds thereof
    • C07C2527/16—Phosphorus; Compounds thereof containing oxygen
    • C07C2527/167—Phosphates or other compounds comprising the anion (PnO3n+1)(n+2)-
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides

Definitions

  • the present invention relates to a new catalytic system, furthermore it relates to processes of producing such catalytic systems as well as their use in selective hydrogenations of C-C triple bonds to C-C double bonds.
  • a Lindlar catalyst is a heterogeneous catalyst that consists of palladium deposited on calcium carbonate or barium sulfate and treated with various forms of lead (Pb).
  • the carrier material is a metal oxide wherein the metal is Ce.
  • the catalytic system according to the present invention does not contain any lead at all. This is in contrast to the typical Lindlar catalyst wherein lead is added deliberately (as so called "poison") to obtain the desired results.
  • the present catalytic system is essentially free from lead (Pb).
  • the carrier material is a metal oxide, wherein the metal is Ce.
  • the metal can be in any oxidation state, which are common for Ce.
  • Ce0 2 is the preferred metal oxide.
  • the present invention also relates to a catalytic system (III), which is catalytic system (I) or (II), wherein the metal oxide is Ce0 2 .
  • Pd-nanoparticles are on the metal oxide carrier.
  • up to 8 weight-% (wt-%), based on the total weight of the catalytic system, of Pd is on the carrier material.
  • at least 0.01 wt-%, based on the total weight of the catalytic system, of Pd is on the carrier material. More preferably 0.01 - 5 wt-%, based on the total weight of the catalytic system, of Pd.
  • the present invention also relates to a catalytic system (IV), which is catalytic system (I), (II) or (III), wherein up to 8 weight-% (wt-%), based on the total weight of the catalytic system, of Pd-nanoparticles are on the carrier material.
  • a catalytic system which is catalytic system (I), (II) or (III), wherein up to 8 weight-% (wt-%), based on the total weight of the catalytic system, of Pd-nanoparticles are on the carrier material.
  • the present invention also relates to a catalytic system (V), which is catalytic system (I), (II), (III) or (IV), wherein at least 0.01 wt-%, based on the total weight of the catalytic system, of Pd-nanoparticles are on the carrier material. Therefore the present invention also relates to a catalytic system (VI), which is catalytic system (I), (II), (III), (IV) or (V), wherein 0.01 - 5 wt-% (preferably 0.1 - 3 wt-%), based on the total weight of the catalytic system, of Pd-nanoparticles are on the carrier material.
  • the new catalytic system can be produced by methods as described below.
  • a Pd(ll) salt (or a mixture of Pd(ll) salts) are suspended/dispersed in a suitable solvent and then sonicated for a short period of time (usually at elevated reaction temperature) and af- terwards this suspension/dispersion (or parts of it) is added to an aqueous suspension of carrier material (the Ce oxide(s)) This mixture is stirred and afterwards the solid is filtered, washed and dried to obtain the catalytic system according to the present invention.
  • the son- ication treatment with ultrasound
  • the frequency used in such process is usually more than 16kHz.
  • the frequency used in such process is usually less than 200 kHz.
  • a preferred range of frequency is 16kHz to 150 kHz.
  • the present invention relates to a process (P) of production of the catalytic systems (I), (II), (III), (IV), (V) or (VI) according to the present invention characterized in that the process comprises an ultrasound (US)-assisted process step.
  • the present invention relates to a process ( ⁇ '), which is process (P) characterized in that the frequency is more than 16 kHz.
  • process (P) which is process (P) characterized in that the frequency is less than 200 kHz.
  • the present invention relates to a process ( ⁇ "'), which is process (P) characterized in that the frequency is in the range of 16kHz to 150 kHz.
  • the reaction temperature of this process is usually elevated, which means that the temperature is more than room temperature.
  • a preferred temperature for the US assisted reaction is above 25 °C. More preferred is a range of temperature of 25 °C to 150 °C.
  • the present invention relates to a process (P ⁇ , which is process (P), ( ⁇ '), (P") or ( ⁇ "'), characterized in that the reaction temperature above 25 °C.
  • the present invention relates to a process (P/), which is process (P ⁇ , wherein the temperature is from 25 °C to 150°C.
  • the reaction time of the ultrasound process can vary.
  • the reaction time is the period of time during which the reaction mixture is treated with Ultra- sound. Usually it is a short reaction time, which is usually less than two hours. Preferably the reaction time is between 5 and 60 minutes.
  • the present invention relates to a process (P 2 ), which is process (P), ( ⁇ '), (P"), ( ⁇ "'), (P ⁇ or (Pi'), wherein the reaction time is less than two hours, preferably between 5 and 60 minutes.
  • the reaction is usually carried out in a suitable solvent or a mixture of solvents.
  • Suitable solvents are water, alcohols, ethers, esters, ketones, amides, and nitriles.
  • Preferred solvents are water, acetone, ethylene glycol, methanol, ethanol, n-propanol and 2- propanol.
  • the present invention also relates to a process (P 3 ), which is process (P), ( ⁇ '), (P"), ( ⁇ "'), (P ⁇ , (P ) or (P 2 ), wherein the reaction is carried out in at least one solvent chosen form the group consisting of water, acetone, ethylene glycol, methanol, ethanol, n- propanol and 2-propanol.
  • a Pd salt or a mixture of Pd salts are used in the process, especially such salts which are low soluble in water.
  • Suitable Pd(ll) salts are Pd(ll)actetate (Pd(OAc) 2 ).
  • Pd(OAc) 2 Pd(ll)actetate
  • the use of acetate salts is also an advantage of the present invention.
  • Pd(ll) chloride salts are used, which cause problems (such as corrosion). Therefore the use of Pd(OAc) 2 is a further advantage of the present invention.
  • the present invention also relates to a process (P 4 ), which is process (P), ( ⁇ '), (P"), ( ⁇ "'), (Pi), (Pi'), (P 2 ) or (P 3 ), wherein Pd(ll)actetate is used.
  • P 4 (Ultrasound assisted) process with cetyldimethyl(2-hydroxyethyl)ammonium di hydrogen phosphate:
  • Cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate which is also known as Lu- viquatTM mono CP AT1 (tradename from BASF) and also as dimethylhexadecyl(2- hydroxyethyl)ammonium dihydrogen phosphate, is used for this process.
  • Lu- viquatTM mono CP AT1 tradename from BASF
  • dimethylhexadecyl(2- hydroxyethyl)ammonium dihydrogen phosphate is used for this process.
  • a water soluble Pd(ll)-salt or a mixture of such salts
  • the present invention relates to a process (P 5 ) of production of the catalytic systems (I), (II), (III), (IV), (V) or (VI) according to the present invention characterized in that the process comprises a process step wherein cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate is used.
  • the reaction is usually carried out in water as solvent.
  • the present invention relates to a process (P 5 ), which is process (P 5 ), wherein the reaction is carried out in water as solvent.
  • concentration of cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate is usually up to 50 wt-%, based on the weight of water and cetyldimethyl(2- hydroxyethyl)ammonium dihydrogen phosphate.
  • concentration of cetyldime- thyl(2-hydroxyethyl)ammonium dihydrogen phosphate is 15 - 40 wt-%.
  • the present invention relates to a process (P 6 ), which is process (P 5 ) or (P 5 ), wherein the concentration of cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate is usually up to 50 wt-%, based on the weight of water and cetyldimethyl(2- hydroxyethyl)ammonium dihydrogen phosphate (Preferably the concentration of cetyldime- thyl(2-hydroxyethyl)ammonium dihydrogen phosphate is 15 - 40 wt-%).
  • the reaction temperature can vary.
  • the reaction is usually carried out at elevated temperatures.
  • the reaction is carried out at a temperature between 30 - 150°C, more preferably at a temperature between 40 - 100°C.
  • the present invention relates to a process (P 7 ), which is process (P 5 ), (Ps ) or (P 6 ), wherein the reaction is carried out at a temperature between 30 - 150°C, preferably at a temperature between 40 - 100 °C.
  • the same process can also be carried out by using a water-insoluble Pd(ll)-salt or a mixture of water-insoluble Pd(ll)-salts, such as Pd(ll)acetate. In this case an ultrasound-assisted step is necessary.
  • the present invention relates to a process (P 8 ), which is process (P 5 ), (P 5 ), (P 6 ) or (P 7 ), wherein the an ultrasound-assisted step is carried out.
  • the present invention relates to a process (P 9 ), which is process (P 5 ), (P 5 ), (P 6 ), (P 7 ) or (P 8 ) wherein the process is carried out as an one-pot procedure in which both the palladium salt and the carrier material were submitted to ultrasound altogether in the presence of cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate in water.
  • a Pd(ll) salt (or a mixture of Pd(ll) salts) is suspended in water and then submitted to ultra- sound to get a dispersion that is then reduced under H 2 pressure with MW heating.
  • the so obtained homogeneous black dispersion (or parts of it) is added to an aqueous suspension of carrier material (the Ce oxide(s)). This mixture is stirred and afterwards the solid is filtered, washed and dried to obtain the catalytic system according to the present invention.
  • carrier material the Ce oxide(s)
  • the present invention relates to process (P 10 ) of production of production of the catalytic systems (I), (II), (III), (IV), (V) or (VI) according to the present invention characterized in that the process comprises first an ultrasound (US)-assisted process step followed by a microwave-assisted heating step.
  • US ultrasound
  • the length of microwave which is applied during the second reaction step can vary, but usually it is chosen in such a way that it can heat the solvent. Therefore the wavelength is usually from 7.5 cm to 15 cm (frequency 2 GHz to 4 GHz). But the wavelengths could also be larger more than 30 cm. The preferred frequency is 2.45 GHz, approximately 12.2 cm. Usually a microwave power of at least 100 W is used. Usually the used microwave power lies in the range of 100 W to 2000 W.
  • the catalytic system (I), (II), (III), (IV), (V) and (VI) according to the present invention is used for selective hydrogenation of C-C triple bonds. Selective hydrogenation are such wherein the C-C triple bond is hydrogenates to the corresponding C-C double. The C-C triple bond is not fully hydrogenated. This is a very important, essential and distinguishing property of the catalytic system according to the present invention. Therefore the present invention also relates to the use (U) of at least one catalytic system (I), (II), (III), (IV), (V) and/or (VI) in a selective hydrogenation of C-C triple bonds.
  • a further embodiment is a selective hydrogenation (SH) of C-C triple bonds, wherein at least one catalytic systems (I), (II), (III), (IV), (V) or (VI) is used.
  • the selective hydrogenation can be carried using commonly used reaction conditions in regard to for example H 2 pressure and reaction temperature.
  • the catalytic systems (I), (II), (III), (IV), (V) and (VI) according to the present invention are particularly suitable to selectively hydrogenate phenyl acetylene (compound (1 )), diphenyl acetylene (compound (2)), buta-2-yn-1 ,4,-diol (compound (3), 3-hexyne (compound (4)) and compounds of formula (5).
  • R 2 is C -C 2 -alkyl.
  • the present invention relates to a selective hydrogenation (SH') of a compound of
  • R 2 is C 1 -C 2 -alkyl
  • the present invention relates to a selective hydrogenation (SH") of a compound of formula (5a), (5b) or (5c)
  • reaction products obtained by the selective hydrogenation are obtained in excellent yield with excellent selectivity.
  • the following examples serve to illustrate the invention. All percentages and parts (if not otherwise stated) are related to the weight and the temperature is given in °C.
  • Pd(OAc) 2 (20 mg) was suspended in 20 mL of ethylene glycol (orange palladium salt was suspended in the solvent, which remained transparent and colourless) and sonicated with a titanium immersion horn (21 .1 kHz at 100 W; 30mm diameter of the horn tip and 170mm length) for 5 min at around 100 °C. After sonication, the suspension became a homogeneous black dispersion that was added dropwise (20 min) to 10 mL of stirring suspension of Ce0 2 (400 mg) with ethylene glycol. The mixture was stirred overnight at room temperature. Then the solid was filtered, washed with methanol and dried under vacuum.
  • Water-insoluble Pd(OAc) 2 (15 mg) was added and the solution (orange solution) was heated in a silicon oil bath to 80°C and sonicated with a titanium immersion horn (21 .1 kHz at 100 W; 30mm diameter of the horn tip and 170mm length) for 5 min. After heating, the solution became a homogeneous black dispersion that was added dropwise to a stirring suspension of Ce0 2 (750 mg) in 10 mL of water (within 20 min). The mixture was stirred overnight at room temperature. The pH was adjusted around 10, then the solid was filtered, washed with water and dried under vacuum.
  • the supported catalysts obtained by Examples 1 - 2 were tested in conventional hydrogenation reactions of selected alkynes: phenyl acetylene (PA) and diphenylacetylene (DPA). Both PA and DPA were hydrogenated with the prepared Pd-catalysts at room temperature and atmospheric hydrogen pressure. 2 mg of Pd-catalyst was added in a 2 mL of hexane containing 0.1 12 mmol of alkyne. Each hydrogenation process was performed in duplicate in one multi-tube reactor and analyzed by GC/MS.
  • PA phenyl acetylene
  • DPA diphenylacetylene
  • the selectivity and the conversion of the selective hydrogenation using the catalytic systems according to the present invention are excellent.

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Abstract

The present invention relates to a new catalytic system, furthermore it relates to processes of producing such catalytic systems as well as their use in selective hydrogenations of C-C triple bonds to C-C double bonds.

Description

PD ON CERIA CATALYTIC SYSTEM FOR SELECTIVE
HYDROGENATIONS OF TRIPLE BONDS
The present invention relates to a new catalytic system, furthermore it relates to processes of producing such catalytic systems as well as their use in selective hydrogenations of C-C triple bonds to C-C double bonds.
Selective hydrogenations (reductions) are important reactions in the field of organic chemistry. The goal of such hydrogenations is getting compounds with C-C double bonds (and not further reducing them to single bonds).
Selective hydrogenations are known in the prior art. Usually there are carried out by using specific kind of catalytic systems. The terms catalytic systems and catalysts are used as synonyms in the context of this patent application. The most important and most widely used types of catalysts are the Lindlar catalysts. A Lindlar catalyst is a heterogeneous catalyst that consists of palladium deposited on calcium carbonate or barium sulfate and treated with various forms of lead (Pb).
Because of the importance of selective hydrogenations there is always a need to provide improved catalytic systems and/or improved selective hydrogenation processes, which are hydrogenations (reductions) of C-C triple bonds to C-C double bonds. The C-C double bonds are not further hydrogenated to C-C single bonds.
Surprisingly it was found that a catalytic system wherein Pd-nanoparticles are deposited on a specific metal oxide carrier, excellent yields, selectivity and conversions can be achieved. Furthermore this catalytic system does not contain any lead at all. This means the catalytic system is essentially free from lead. This means that it can contain Pb in traces (but no Pb is added intentionally). Therefore the present invention relates to a catalytic system (I) comprising
(a) Pd-nanoparticles on a
(b) carrier material,
characterized in that the carrier material is a metal oxide wherein the metal is Ce. As stated above the catalytic system according to the present invention does not contain any lead at all. This is in contrast to the typical Lindlar catalyst wherein lead is added deliberately (as so called "poison") to obtain the desired results. The present catalytic system is essentially free from lead (Pb).
In the context of the present invention the terms "catalyst(s)" and "catalytic system(s)" are used synonymously. Therefore the present invention also relates to a catalytic system (II), which is catalytic system (I), which does not contain any lead (= which is essentially free from lead).
The carrier material is a metal oxide, wherein the metal is Ce. The metal can be in any oxidation state, which are common for Ce.
Ce02 is the preferred metal oxide.
Therefore the present invention also relates to a catalytic system (III), which is catalytic system (I) or (II), wherein the metal oxide is Ce02.
Pd-nanoparticles are on the metal oxide carrier. Preferably, up to 8 weight-% (wt-%), based on the total weight of the catalytic system, of Pd is on the carrier material. Usually at least 0.01 wt-%, based on the total weight of the catalytic system, of Pd is on the carrier material. More preferably 0.01 - 5 wt-%, based on the total weight of the catalytic system, of Pd. Most preferably 0.1 - 3 wt-%, based on the total weight of the catalytic system, of Pd.
Therefore the present invention also relates to a catalytic system (IV), which is catalytic system (I), (II) or (III), wherein up to 8 weight-% (wt-%), based on the total weight of the catalytic system, of Pd-nanoparticles are on the carrier material.
Therefore the present invention also relates to a catalytic system (V), which is catalytic system (I), (II), (III) or (IV), wherein at least 0.01 wt-%, based on the total weight of the catalytic system, of Pd-nanoparticles are on the carrier material. Therefore the present invention also relates to a catalytic system (VI), which is catalytic system (I), (II), (III), (IV) or (V), wherein 0.01 - 5 wt-% (preferably 0.1 - 3 wt-%), based on the total weight of the catalytic system, of Pd-nanoparticles are on the carrier material. The new catalytic system can be produced by methods as described below.
Suitable methods are i.e. Ultrasound (US)-assisted method for the reduction-by-solvent of Pd(ll), (sonochemically = ultrasound-assisted) with Luviquat™ in water, and US- and microwave (MW)-assisted method under hydrogen pressure. In the following these three methods are discussed in further details.
(1) Ultrasound-assisted reduction-by-solvent of Pd(ll):
A Pd(ll) salt (or a mixture of Pd(ll) salts) are suspended/dispersed in a suitable solvent and then sonicated for a short period of time (usually at elevated reaction temperature) and af- terwards this suspension/dispersion (or parts of it) is added to an aqueous suspension of carrier material (the Ce oxide(s)) This mixture is stirred and afterwards the solid is filtered, washed and dried to obtain the catalytic system according to the present invention. The son- ication (treatment with ultrasound) can be carried by commonly known Ultrasound devices. The frequency used in such process is usually more than 16kHz. The frequency used in such process is usually less than 200 kHz.
A preferred range of frequency is 16kHz to 150 kHz.
It is clear that during the process the frequency can be varied. Therefore the present invention relates to a process (P) of production of the catalytic systems (I), (II), (III), (IV), (V) or (VI) according to the present invention characterized in that the process comprises an ultrasound (US)-assisted process step.
Furthermore the present invention relates to a process (Ρ'), which is process (P) characterized in that the frequency is more than 16 kHz.
Furthermore the present invention relates to a process (P"), which is process (P) characterized in that the frequency is less than 200 kHz.
Furthermore the present invention relates to a process (Ρ"'), which is process (P) characterized in that the frequency is in the range of 16kHz to 150 kHz. The reaction temperature of this process is usually elevated, which means that the temperature is more than room temperature. A preferred temperature for the US assisted reaction is above 25 °C. More preferred is a range of temperature of 25 °C to 150 °C.
For the experiments carried out for this patent application commercially available ultrasound laboratory equipment was used from DANACAMERINI s.a.s. di Buffa Cesare & C, Str. del Fioccardo, Turin, Italy. Other useful similar equipment can be bought from Emerson Industrial Automation (Branson Sonifier 250/450).
Furthermore the present invention relates to a process (P^, which is process (P), (Ρ'), (P") or (Ρ"'), characterized in that the reaction temperature above 25 °C.
Furthermore the present invention relates to a process (P/), which is process (P^, wherein the temperature is from 25 °C to 150°C.
The reaction time of the ultrasound process can vary. In the context of the present invention the reaction time is the period of time during which the reaction mixture is treated with Ultra- sound. Usually it is a short reaction time, which is usually less than two hours. Preferably the reaction time is between 5 and 60 minutes.
Furthermore the present invention relates to a process (P2), which is process (P), (Ρ'), (P"), (Ρ"'), (P^ or (Pi'), wherein the reaction time is less than two hours, preferably between 5 and 60 minutes.
The reaction is usually carried out in a suitable solvent or a mixture of solvents.
Suitable solvents are water, alcohols, ethers, esters, ketones, amides, and nitriles.
Preferred solvents are water, acetone, ethylene glycol, methanol, ethanol, n-propanol and 2- propanol.
Therefore the present invention also relates to a process (P3), which is process (P), (Ρ'), (P"), (Ρ"'), (P^, (P ) or (P2), wherein the reaction is carried out in at least one solvent chosen form the group consisting of water, acetone, ethylene glycol, methanol, ethanol, n- propanol and 2-propanol.
A Pd salt or a mixture of Pd salts are used in the process, especially such salts which are low soluble in water. Suitable Pd(ll) salts are Pd(ll)actetate (Pd(OAc)2). The use of acetate salts is also an advantage of the present invention. In the prior art usually Pd(ll) chloride salts are used, which cause problems (such as corrosion). Therefore the use of Pd(OAc)2 is a further advantage of the present invention.
Therefore the present invention also relates to a process (P4), which is process (P), (Ρ'), (P"), (Ρ"'), (Pi), (Pi'), (P2) or (P3), wherein Pd(ll)actetate is used. (2) (Ultrasound assisted) process with cetyldimethyl(2-hydroxyethyl)ammonium di hydrogen phosphate:
Cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate, which is also known as Lu- viquat™ mono CP AT1 (tradename from BASF) and also as dimethylhexadecyl(2- hydroxyethyl)ammonium dihydrogen phosphate, is used for this process. To a diluted aqueous solution of cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate a water soluble Pd(ll)-salt (or a mixture of such salts) is added and this reaction mixture is heated for a period of time. Afterwards the so obtained dispersion (or parts of it) is added to an aqueous suspension of carrier material (the Ce oxide(s)). This mixture is stirred and afterwards the pH of this reaction mixture is adjusted to about 10 and then the solid is filtered, washed and dried to obtain the catalytic system according to the present invention. Therefore the present invention relates to a process (P5) of production of the catalytic systems (I), (II), (III), (IV), (V) or (VI) according to the present invention characterized in that the process comprises a process step wherein cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate is used.
The reaction is usually carried out in water as solvent.
Therefore the present invention relates to a process (P5), which is process (P5), wherein the reaction is carried out in water as solvent. The concentration of cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate is usually up to 50 wt-%, based on the weight of water and cetyldimethyl(2- hydroxyethyl)ammonium dihydrogen phosphate. Preferably the concentration of cetyldime- thyl(2-hydroxyethyl)ammonium dihydrogen phosphate is 15 - 40 wt-%.
Therefore the present invention relates to a process (P6), which is process (P5) or (P5), wherein the concentration of cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate is usually up to 50 wt-%, based on the weight of water and cetyldimethyl(2- hydroxyethyl)ammonium dihydrogen phosphate (Preferably the concentration of cetyldime- thyl(2-hydroxyethyl)ammonium dihydrogen phosphate is 15 - 40 wt-%). The reaction temperature can vary. The reaction is usually carried out at elevated temperatures. Preferably, the reaction is carried out at a temperature between 30 - 150°C, more preferably at a temperature between 40 - 100°C.
Therefore the present invention relates to a process (P7), which is process (P5), (Ps ) or (P6), wherein the reaction is carried out at a temperature between 30 - 150°C, preferably at a temperature between 40 - 100 °C.
The same process can also be carried out by using a water-insoluble Pd(ll)-salt or a mixture of water-insoluble Pd(ll)-salts, such as Pd(ll)acetate. In this case an ultrasound-assisted step is necessary.
Therefore the present invention relates to a process (P8), which is process (P5), (P5), (P6) or (P7), wherein the an ultrasound-assisted step is carried out.
Furthermore is also possible to carry out this process as an one-pot procedure in which both the palladium salt and the carrier material (=(the Ce oxide(s)) were submitted to ultrasound altogether in the presence of cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate in water.
Therefore the present invention relates to a process (P9), which is process (P5), (P5), (P6), (P7) or (P8) wherein the process is carried out as an one-pot procedure in which both the palladium salt and the carrier material were submitted to ultrasound altogether in the presence of cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate in water.
(3) Ultrasound (US)- and microwave (MW)-assisted process under hydrogen pressure
A Pd(ll) salt (or a mixture of Pd(ll) salts) is suspended in water and then submitted to ultra- sound to get a dispersion that is then reduced under H2 pressure with MW heating.
The so obtained homogeneous black dispersion (or parts of it) is added to an aqueous suspension of carrier material (the Ce oxide(s)). This mixture is stirred and afterwards the solid is filtered, washed and dried to obtain the catalytic system according to the present invention.
Therefore the present invention relates to process (P10) of production of production of the catalytic systems (I), (II), (III), (IV), (V) or (VI) according to the present invention characterized in that the process comprises first an ultrasound (US)-assisted process step followed by a microwave-assisted heating step.
All reaction conditions for the ultrasound assisted process step as already defined under (1 ) are also to be applied for this ultrasound assisted process step. After the ultrasound (US)-assisted process step, a microwave (MW)-heating step is carried out.
The length of microwave which is applied during the second reaction step can vary, but usually it is chosen in such a way that it can heat the solvent. Therefore the wavelength is usually from 7.5 cm to 15 cm (frequency 2 GHz to 4 GHz). But the wavelengths could also be larger more than 30 cm. The preferred frequency is 2.45 GHz, approximately 12.2 cm. Usually a microwave power of at least 100 W is used. Usually the used microwave power lies in the range of 100 W to 2000 W.
For the experiments carried out for this patent application commercially available microwave lab equipment was used (SynthWAVE from MLS GmbH (Germany)).
It also possible to use a process wherein just a MW-step (and no US-step) is carried out.
The catalytic system (I), (II), (III), (IV), (V) and (VI) according to the present invention is used for selective hydrogenation of C-C triple bonds. Selective hydrogenation are such wherein the C-C triple bond is hydrogenates to the corresponding C-C double. The C-C triple bond is not fully hydrogenated. This is a very important, essential and distinguishing property of the catalytic system according to the present invention. Therefore the present invention also relates to the use (U) of at least one catalytic system (I), (II), (III), (IV), (V) and/or (VI) in a selective hydrogenation of C-C triple bonds.
A further embodiment is a selective hydrogenation (SH) of C-C triple bonds, wherein at least one catalytic systems (I), (II), (III), (IV), (V) or (VI) is used.
The selective hydrogenation can be carried using commonly used reaction conditions in regard to for example H2 pressure and reaction temperature.
The catalytic systems (I), (II), (III), (IV), (V) and (VI) according to the present invention are particularly suitable to selectively hydrogenate phenyl acetylene (compound (1 )), diphenyl acetylene (compound (2)), buta-2-yn-1 ,4,-diol (compound (3), 3-hexyne (compound (4)) and compounds of formula (5).
wherein is Ci - C2o alkyl or C3 - C2o alkenyl,
and R2 is C -C2-alkyl.
Therefore the present invention relates to a selective hydrogenation (SH') of a compound of
(4) or (5)
(2)
wherein is Ci - C20 alkyl or C3 - C20 alkenyl,
and R2 is C1-C2-alkyl,
characterized in that a catalytic system (I), (II), (III), (IV), (V) and/or (VI) is used. ds are the following
The following compounds of formulae (5a), (5b) and (5c) are preferred compounds of formula (5):
Therefore the present invention relates to a selective hydrogenation (SH") of a compound of formula (5a), (5b) or (5c)
characterized in that a catalytic system (I), (II), (III), (IV), (V) and/or (VI) is used.
The reaction products obtained by the selective hydrogenation are obtained in excellent yield with excellent selectivity. The following examples serve to illustrate the invention. All percentages and parts (if not otherwise stated) are related to the weight and the temperature is given in °C.
Examples
Process of production of the catalysts
Examples 1
Pd(OAc)2 (20 mg) was suspended in 20 mL of ethylene glycol (orange palladium salt was suspended in the solvent, which remained transparent and colourless) and sonicated with a titanium immersion horn (21 .1 kHz at 100 W; 30mm diameter of the horn tip and 170mm length) for 5 min at around 100 °C. After sonication, the suspension became a homogeneous black dispersion that was added dropwise (20 min) to 10 mL of stirring suspension of Ce02 (400 mg) with ethylene glycol. The mixture was stirred overnight at room temperature. Then the solid was filtered, washed with methanol and dried under vacuum.
This process was carried out with Ce02 as carrier material. The following table summarized the various catalyst, which have been produced. The weight-% (wt-%) in the table is related to the total weight of the dried catalyst.
Example 2
500 μί of hexadecyl(2-hydroxyethyl)dimethylammonium dihydrogen phosphate 30% solution in water (Luviquat mono CP AT1 ) was diluted with distilled water to a final volume of 10 mL.
Water-insoluble Pd(OAc)2 (15 mg) was added and the solution (orange solution) was heated in a silicon oil bath to 80°C and sonicated with a titanium immersion horn (21 .1 kHz at 100 W; 30mm diameter of the horn tip and 170mm length) for 5 min. After heating, the solution became a homogeneous black dispersion that was added dropwise to a stirring suspension of Ce02 (750 mg) in 10 mL of water (within 20 min). The mixture was stirred overnight at room temperature. The pH was adjusted around 10, then the solid was filtered, washed with water and dried under vacuum.
This process was carried out with Ce02 as carrier material. The following table summarized the details of the catalyst, which has been produced. The weight-% (wt-%) in the table is re- lated to the total weight of the dried catalyst. Exp. Pd-conc. Carrier material
[wt-%]
2 0.93 Ce02
Examples 3a - 3b
Selective hydrogenation using the catalysts of examples 1 - 2
The supported catalysts obtained by Examples 1 - 2 were tested in conventional hydrogenation reactions of selected alkynes: phenyl acetylene (PA) and diphenylacetylene (DPA). Both PA and DPA were hydrogenated with the prepared Pd-catalysts at room temperature and atmospheric hydrogen pressure. 2 mg of Pd-catalyst was added in a 2 mL of hexane containing 0.1 12 mmol of alkyne. Each hydrogenation process was performed in duplicate in one multi-tube reactor and analyzed by GC/MS.
In the following table the results of the PA hydrogenation are summarized
The selectivity and the conversion of the selective hydrogenation using the catalytic systems according to the present invention are excellent.

Claims

Claims
1 . A catalytic system (I) comprising
(a) Pd-nanoparticles on a
(b) carrier material,
characterized in that the carrier material is a metal oxide wherein the metal is Ce.
2. Catalytic system according to claim 1 characterised in that the catalytic system is essentially free from Pb.
Catalytic system according to claim 1 or 2 wherein the metal oxide is Ce02.
Catalytic system according to any of the preceding claims wherein up to 8 weight-% (wt-%), based on the total weight of the catalytic system, of Pd is on the carrier mate- rial.
5. Catalytic system according to any of the preceding claims wherein at least 0.01 wt- %, based on the total weight of the catalytic system, of Pd is on the carrier material.
6. Catalytic system according to any of the preceding claims, wherein 0.01 - 5 wt-%, based on the total weight of the catalytic system, of Pd is on the carrier material.
7. Process of production of the catalytic systems according to any of the preceding claims characterized in that the process comprises an ultrasound (US)-assisted pro- cess step and/or a microwave-heating step.
8. Process of production of the catalytic systems according to any of claims 1 - 6, characterized in that the process comprises an process step wherein hexadecyl(2- hydroxyethyl)dimethylammonium dihydrogen phosphate is used.
9. Use of at least one catalytic system according to any of the claims 1 - 6 in a selective hydrogenation of a C-C triple bond.
Selective hydrogenation of C-C triple bonds characterized in that at least one catalytic system according to claims 1 - 6 is used.
1. Selective hydrogenation according to claim 10, characterized in that one of the following compound is hydrogenated selectively
wherein is Ci - C20 alkyl or C3 - C20 alkenyl,
and R2 is C1-C2-alkyl.
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