EP2438215A1 - Procédé de préparation de biaryle-alcools dissymétriques - Google Patents
Procédé de préparation de biaryle-alcools dissymétriquesInfo
- Publication number
- EP2438215A1 EP2438215A1 EP10724438A EP10724438A EP2438215A1 EP 2438215 A1 EP2438215 A1 EP 2438215A1 EP 10724438 A EP10724438 A EP 10724438A EP 10724438 A EP10724438 A EP 10724438A EP 2438215 A1 EP2438215 A1 EP 2438215A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- ortho
- group
- alkoxyarylalkohole
- alcohols
- alkyl
- 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.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B3/00—Electrolytic production of organic compounds
- C25B3/20—Processes
- C25B3/29—Coupling reactions
Definitions
- the invention relates to a process for the preparation of unsymmetrical biaryl alcohols, which is carried out by anodic dehydrodimerization of substituted ortho-alkoxy aryl alcohols in the presence of partially and / or perfluorinated mediators and a conductive salt.
- Biaryls are known as such and are used industrially. Compounds such as 3,3 ', 5,5'-tetramethylbiphenyl-2,2'-diol are of great interest as backbones for ligands.
- One possible approach to this class of compounds is the (electrochemical) oxidative dimerization of phenols. However, this is often unselective.
- Diamond electrodes can be realized using conductive salts and fluorinated mediators as described by A. Kirste, M. Nieger, IM Malkowsky, F. Stecker, A. Fischer, SR Waldvogel in Chem. Eur. J. 2009, 15, 2273 and described in WO-A 2006/077204. A process for preparing the unsymmetrical biaryl alcohols is not described.
- the object of the present invention is to provide a process which enables the selective and efficient anodic dehydrodimerization of substituted ortho-alkoxyaryl alcohols to unsymmetrical biaryl alcohols.
- the process according to the invention is advantageous if the OH group of the ortho-alkoxyaryl alcohols used is bound directly to the aromatic compound.
- the process according to the invention is advantageous if the substituted orthoalkoxyaryl alcohols used are identical.
- the process according to the invention is advantageous if the substituted orthoalkoxyaryl alcohols used are mononuclear or dinuclear.
- the process according to the invention is advantageous if the dimerization takes place in the ortho position to the one and in the meta position relative to the other alcohol group of the ortho-alkoxyaryl alcohols.
- the process according to the invention is advantageous if the mediators used are partially and / or perfluorinated alcohols and / or acids.
- the process according to the invention is advantageous if 1, 1, 1, 3,3,3-hexafluoroisopropanol and / or trifluoroacetic acid are used as mediators.
- the process according to the invention is advantageous, in which the conductive salts used are those which are selected from the group of alkali metal, alkaline earth metal, tetra (C 1 to C 6 alkyl) ammonium salts.
- the counterions of the conducting salts are selected from the group consisting of sulfate, hydrogensulfate, alkyl sulfates, aryl sulfates, halides, phosphates, carbonates, alkyl phosphates, alkyl carbonates, nitrate, alcoholates, tetrafluoroborate, hexafluorophosphate and perchlorate.
- the process according to the invention is advantageous if no further solvent is used for the electrolysis.
- the method according to the invention is advantageous if a nickel cathode is used.
- the process according to the invention is advantageous if a flow cell is used for the electrolysis.
- the process according to the invention is advantageous when current densities of 1 to 1000 mA / cm 2 are used.
- the process according to the invention is advantageous if the electrolysis is carried out at temperatures in the range from -20 to 100 ° C. and atmospheric pressure.
- the process according to the invention is advantageous if 4-methylguajacol is used as ortho-alkoxyaryl alcohol.
- the inventive method when the anode is selected from the group of graphite and boron doped diamond electrode.
- ortho-alkoxyaryl alcohol is understood as meaning aromatic alcohols which are substituted ortho-substituted by an alkoxy group and in which the hydroxyl group is bonded directly to the aromatic nucleus.
- the aromatic which is based on the ortho-Alkoxyarylalkohol, may be mononuclear or polynuclear.
- the aromatic is preferably mononuclear (phenol derivatives) according to formula I or binuclear (naphthol derivatives) according to formula II, particular preference is given to mononuclear aromatics.
- the alkoxy group (OAlk) of the ortho-alkoxyaryl alcohols which are used in the process according to the invention are C.sub.1- to C.sub.10-alkoxy group, preferably methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, tert-butyl Butoxy groups, more preferably, methoxy, ethoxy, n-propoxy, most preferably methoxy groups.
- the ortho-Alkoxyarylalkohle can carry further substituents R1 to R6.
- R 1 to R 6 are independently selected from the group of C 1 -C 10 -alkyl groups, halogens, C 1 -C 10 -alkoxy groups, alkylene or arylene radicals interrupted by oxygen or sulfur, C 1 -C 10 -alkoxycarboxylic, nitrile, nitro- and Ci-Cio-Alkoxycarbamoyl phenomenon.
- the substituents are preferably selected from the group of methyl, ethyl, n-propyl, isopropyl, n-butyl, trifluoromethyl, fluorine, chlorine, bromine, iodine, methoxy, ethoxy, methylene, ethylene, propylene, isopropylene, benzylidene, nitrile, nitro ,
- the substituents are particularly preferably selected from the group of methyl, methoxy, methylene, ethylene, trifluoromethyl, fluorine and bromine.
- the unsymmetrical biaryl alcohol is produced electrochemically, with the corresponding ortho-alkoxyaryl alcohol being anodically oxidized.
- the process according to the invention is referred to below as electrodimerization. It has surprisingly been found that the unsymmetrical biaryl alcohols are produced selectively and in high yield by the process according to the invention using mediators. Furthermore, it has been found that by the These methods can be applied to undivided cell structures as well as solvent-free methods.
- the electrolyte solution is worked up by general separation methods.
- the electrolyte solution is generally first distilled and recovered the individual compounds in the form of different fractions separately. Further purification can be carried out, for example, by crystallization, distillation, sublimation or chromatographic.
- Electrodes selected from the group of iron, steel, stainless steel, nickel, noble metals such as platinum, graphite, carbon materials such as the diamond electrodes are used for the process according to the invention. These diamond electrodes are formed by applying one or more diamond layers to a substrate. Possible support materials are niobium, silicon, tungsten, titanium, silicon carbide, tantalum, graphite or ceramic supports such as titanium suboxide. However, a support of niobium, titanium or silicon is preferred for the method according to the invention, very particular preference is given to a support of niobium, if a diamond electrode is used.
- the anode is selected from the group of graphite and diamond electrode, wherein the diamond electrode may also be doped with other elements. Boron and nitrogen are preferred as doping elements. The process according to the invention with a boron-doped diamond electrode (BDD electrode) as anode is very particularly preferred.
- the cathode material is selected from the group of iron, steel, stainless steel, nickel, precious metals such as platinum, graphite, carbon materials and diamantelekt- roden.
- the cathode is selected from the group of nickel, steel and stainless steel.
- the cathode is particularly preferably made of nickel.
- Preferred electrode material combinations for anode and cathode are a combination of graphite anode and nickel cathode and the combination of boron-doped diamond anode and nickel cathode.
- Partially and / or perfluorinated alcohols and / or acids preferably perfluorinated alcohols and carboxylic acids, very particularly preferably 1, 1, 1, 3, 3, 3-hexafluoroisopropanol or trifluoroacetic acid are used as mediators in the process according to the invention.
- the electrolysis is carried out in the usual, known in the art electrolysis cells.
- Suitable electrolysis cells are known to the person skilled in the art. Preferably, one works continuously in undivided flow cells or discontinuously in beaker cells.
- Particularly suitable are bipolar switched capillary gap cells or Plattenstapelzellen, in which the electrodes are designed as plates and are arranged plane-parallel as in Ullmann's Encyclopedia of Industrial Chemistry, 1999 electronic release, Sixth Edition, Wiley-VCH-Weinheim, (doi: 10 1002 / 14356007.a09_183.pub2) and in Electrochemistry, Chapter 3.5. special cell designs as well as Chapter 5, Organic Electrochemistry, Subchapter 5.4.3.2 Cell Design.
- the current densities at which the process is carried out are generally 1 to 1000, preferably 5 to 100 mA / cm 2 .
- the temperatures are usually from -20 to 100 ° C., preferably from 10 to 60 ° C.
- the reaction is generally carried out under atmospheric pressure. Higher pressures are preferably used when operating at higher temperatures to avoid boiling of the co-solvents or mediators.
- the ortho-alkoxyaryl alcohol compound are dissolved in a suitable solvent.
- suitable solvents known to the person skilled in the art, preferably solvents from the group of polar protic and polar aprotic solvents, are suitable.
- the ortho-alkoxyaryl alcohol compound itself serves as solvent and reagent.
- polar aprotic solvents include nitriles, amides, carbonates, ethers, ureas, chlorinated hydrocarbons.
- particularly preferred polar aprotic solvents include acetonitrile, dimethylformamide, dimethyl sulfoxide, propylene carbonate and dichloromethane.
- polar protic solvents include alcohols, carboxylic acids and amides.
- particularly preferred polar protic solvents include methanol, ethanol, propanol, butanol, pentanol and hexanol. These may also be partially or fully halogenated, such as 1, 1, 1, 3,3,3-hexafluoroisopropanol (HFIP) or trifluoroacetic acid (TFA).
- HFIP 1, 1, 1, 1, 3,3,3-hexafluoroisopropanol
- TFA trifluoroacetic acid
- the electrolysis solution is added to customary cosolvents.
- these are the inert solvents customary in organic chemistry with a high oxidation potential. Examples include its dimethyl carbonate, propylene carbonate, tetrahydrofuran, dimethoxyethane, acetonitrile or dimethylformamide.
- Conducting salts which are contained in the electrolysis solution are generally alkali metal, alkaline earth metal, tetra (C 1 -C 6 -alkyl) ammonium, preferably tri (C 1 -C 6 -alkyl) methylammonium salts.
- Suitable counterions are sulfates, hydrogen sulfates, alkyl sulfates, aryl sulfates, halides, phosphates, carbonates, alkyl phosphates, alkyl carbonates, nitrates, alkoxides, tetrafluoroborate, hexafluorophosphate or perchlorate.
- the acids derived from the abovementioned anions are suitable as conductive salts.
- MTBS methyltributylammonium methylsulfates
- MTES methyltriethylammonium methylsulfate
- TABF tetrabutylammonium, tetrafluoroborate
- the electrolyte consisting of 2.76 g of 4-methylguajacol, 0.68 g of methyltriethylammonium methyl sulfate (MTES) and 30 ml of hexafluoroisopropanol (HFIP) according to Table 1 submitted.
- MTES methyltriethylammonium methyl sulfate
- HFIP hexafluoroisopropanol
- the electrolysis is carried out under galvanostatic control and at current densities between 2.8-9.5 mA / cm 2 .
- the reaction is stopped after reaching the set charge limit (1 F per mole of 4-methylguajacol).
- the cooled reaction mixture is transferred with about 20 ml of toluene into a flask, from which toluene and the fluorinated solvent used are almost completely removed on a rotary evaporator. Excess phenol can be recovered by short path distillation at 1, 0 * 10 1 mbar and 125 0 C.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP10724438A EP2438215A1 (fr) | 2009-06-05 | 2010-06-01 | Procédé de préparation de biaryle-alcools dissymétriques |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09162076 | 2009-06-05 | ||
EP10724438A EP2438215A1 (fr) | 2009-06-05 | 2010-06-01 | Procédé de préparation de biaryle-alcools dissymétriques |
PCT/EP2010/057619 WO2010139687A1 (fr) | 2009-06-05 | 2010-06-01 | Procédé de préparation de biaryle-alcools dissymétriques |
Publications (1)
Publication Number | Publication Date |
---|---|
EP2438215A1 true EP2438215A1 (fr) | 2012-04-11 |
Family
ID=42358670
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP10724438A Withdrawn EP2438215A1 (fr) | 2009-06-05 | 2010-06-01 | Procédé de préparation de biaryle-alcools dissymétriques |
Country Status (5)
Country | Link |
---|---|
US (1) | US8747645B2 (fr) |
EP (1) | EP2438215A1 (fr) |
JP (1) | JP2012528825A (fr) |
CN (1) | CN102459707A (fr) |
WO (1) | WO2010139687A1 (fr) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5705216B2 (ja) * | 2009-06-05 | 2015-04-22 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | アレーンの陽極クロス脱水素二量化法 |
DE102013203865A1 (de) * | 2013-03-07 | 2014-09-11 | Evonik Industries Ag | Elektrochemische Kupplung zweier Phenole, welche sich in ihrem Oxidationspotential unterscheiden |
DE102013211744A1 (de) | 2013-06-21 | 2014-12-24 | Evonik Industries Ag | Elektrochemisches Verfahren zur Herstellung von symmetrischen Biphenolen unter Verwendung einer Glaskohlenstoffanode |
DE102013211745A1 (de) | 2013-06-21 | 2014-12-24 | Evonik Industries Ag | Elektrochemisches Verfahren zur Herstellung von symmetrischen Biphenolen unter Verwendung von Essigsäure als Elektrolyt |
US9950979B2 (en) | 2014-05-26 | 2018-04-24 | Evonik Degussa Gmbh | Method for producing asymmetrical biphenols using selenium dioxide |
DE102014209976A1 (de) | 2014-05-26 | 2015-11-26 | Evonik Degussa Gmbh | Verfahren zur Herstellung von 2,2'-Biphenolen unter Verwendung von Selendioxid und halogeniertem Lösungsmittel |
DE102014209967A1 (de) | 2014-05-26 | 2015-12-17 | Evonik Degussa Gmbh | Verfahren zur Herstellung von 2,2'-Biphenolen unter Verwendung von Selendioxid |
SG10201601501QA (en) | 2015-03-05 | 2016-10-28 | Evonik Degussa Gmbh | Preparation of 2,2`-biaryls in the presence of molybdenum(v) chloride |
EP3095776A1 (fr) | 2015-05-20 | 2016-11-23 | Evonik Degussa GmbH | Couplage d'un phénol et d'un arène à l'aide d'anhydride sélénieux |
DE102015216000A1 (de) * | 2015-08-21 | 2017-02-23 | Evonik Degussa Gmbh | Verfahren zur Herstellung von symmetrischen Pincerliganden aus der Gruppe der m-Terphenylverbindungen |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3992435A (en) * | 1975-04-07 | 1976-11-16 | Standard Oil Company (Indiana) | Process for electrolytic synthesis of polyalkylbiphenylpolycarboxylic acid compounds |
US4101391A (en) | 1976-01-05 | 1978-07-18 | Monsanto Company | Electrolytic oxidative methyl-methyl coupling of cresol salts |
JPH0243388A (ja) * | 1988-08-03 | 1990-02-13 | Mitsubishi Kasei Corp | 4,4’−ジヒドロキシビフェニル類の製造法 |
EP0663378B1 (fr) * | 1993-12-11 | 1999-03-31 | Hoechst Aktiengesellschaft | Procédé pour la préparation de 2,2'-diméthyle-1,1'-binaphthalène et 2,7'-diméthyle-1,1'-binaphthalène |
DE4411024A1 (de) * | 1994-03-30 | 1995-12-21 | Hoechst Ag | Verfahren zur Herstellung von 4,4'-Dimethyl-1,1'-binaphthyl |
JPH08245459A (ja) * | 1995-03-16 | 1996-09-24 | Dainippon Ink & Chem Inc | フェノール性水酸基含有縮合多環式化合物の二量化物の製法 |
DE19641344A1 (de) | 1995-10-17 | 1997-04-24 | Basf Ag | Verfahren zur Herstellung von Biarylen |
JPH09176074A (ja) * | 1995-12-28 | 1997-07-08 | Kibun Foods Inc | 抗菌・抗カビ・抗炎症活性物質とその製造方法 |
FR2803856B1 (fr) * | 2000-01-13 | 2002-07-05 | Atofina | Synthese de l'hydroxyde de tetramethylammonium |
DE102004005508A1 (de) | 2004-02-04 | 2005-08-25 | Basf Ag | Anodische Dimerisierung substituierter Benzole |
DE102005003012A1 (de) * | 2005-01-21 | 2006-07-27 | Basf Ag | Anodische Dimerisierung von Hydroxy-substituierten Aromaten |
CN100436649C (zh) * | 2005-01-28 | 2008-11-26 | 华东师范大学 | 联苯的电化学合成方法 |
US7918987B2 (en) * | 2006-05-15 | 2011-04-05 | Akzo Nobel N.V. | Electrochemical process to prepare a halogenated carbonyl group-containing compound |
WO2010023258A1 (fr) | 2008-09-01 | 2010-03-04 | Basf Se | Procédé de déhydrodimérisation anodique d’arylalcools substitués |
JP5705216B2 (ja) * | 2009-06-05 | 2015-04-22 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | アレーンの陽極クロス脱水素二量化法 |
-
2010
- 2010-06-01 US US13/375,100 patent/US8747645B2/en not_active Expired - Fee Related
- 2010-06-01 CN CN2010800245846A patent/CN102459707A/zh active Pending
- 2010-06-01 EP EP10724438A patent/EP2438215A1/fr not_active Withdrawn
- 2010-06-01 WO PCT/EP2010/057619 patent/WO2010139687A1/fr active Application Filing
- 2010-06-01 JP JP2012513596A patent/JP2012528825A/ja active Pending
Non-Patent Citations (1)
Title |
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See references of WO2010139687A1 * |
Also Published As
Publication number | Publication date |
---|---|
US20120067736A1 (en) | 2012-03-22 |
CN102459707A (zh) | 2012-05-16 |
WO2010139687A1 (fr) | 2010-12-09 |
JP2012528825A (ja) | 2012-11-15 |
US8747645B2 (en) | 2014-06-10 |
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