Classifications

• • 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
  • C07C41/34—Separation; Purification; Stabilisation; Use of additives
• • C—CHEMISTRY; METALLURGY
  • 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
  • C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
  • C07C37/70—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
  • C07C37/82—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by solid-liquid treatment; by chemisorption
• • 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
  • C07C41/34—Separation; Purification; Stabilisation; Use of additives
  • C07C41/36—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C43/00—Ethers; Compounds having groups, groups or groups
  • C07C43/02—Ethers
  • C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
  • C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups

Definitions

• the present invention provides a method of separating phenolic compounds in salified form from a reaction mixture comprising them.
• the invention relates to the separation of guaiacol or of guaethol in salified form from the synthesis mixtures comprising them.
• the invention is directed more particularly to the recovery of guaiacol in the form of sodium salt, present in excess amount, during the synthesis of vanillin or 4-hydroxy-3-methoxybenzaldehyde.
• Hydroxyaromatic and alkoxyaromatic aldehydes are very important products, which are used as flavors and fragrances and as intermediates in numerous fields, such as, for example, agrochemicals, pharmacy, cosmetology, and other industries.
• the phenolic compound is generally involved in a salified form, for example, in the form of a sodium salt.
• vanillin One conventional route to vanillin involves a condensation reaction of glyoxylic acid with guaiacol, in basic medium, to give 4-hydroxy-3-methoxymandelic acid. This product is then oxidized to produce vanillin.
• the reaction is commonly conducted in the presence of sodium hydroxide and with an excess of guaiacol, with glyoxylic acid being the deficit reactant.
• an aqueous reaction mixture that comprises the sodium salt of 4-hydroxy-3-methoxymandelic acid, the precursor to vanillin, secondary products, such as the sodium salts of 2-hydroxy-3-methoxymandelic acid and 4-hydroxy-5-methoxy-1,3-dimandelic acid, and a greater or lesser excess of sodium guaiacolate.
• guaiacol is in the form of sodium guaiacolate and is present alongside phenolic compounds which are also salified and have a closely related structure.
• the unconverted guaiacol is then extracted from the acid solution by an extraction treatment using a hydrocarbon, for example, benzene or toluene.
• a hydrocarbon for example, benzene or toluene.
• the drawback of a method of this kind is that it employs an organic solvent, thereby giving rise to additional distillation operations in order to be able to recycle the organic solvent and the substrate recovered. Moreover, in the course of the distillation, there are secondary reactions which lead to the formation of heavy products.
• the guaiacol recovered must be salified again in order to be introduced into the condensation reaction with glyoxylic acid.
• reaction mixture comprising the mandelic compounds with a free hydroxyl group, must be salified again in order to be introduced into the oxidation reaction that allows vanillin to be obtained.
• the invention provides a method that allows the excess of phenolic starting compound in salified form, especially sodium guaiacolate, to be recovered, by a method which does not involve this step of neutralizing sodium guaiacolate to guaiacol, with the attendant need for said guaiacol to be extracted using an organic solvent which must subsequently be separated by distillation.
• a method has now been found, and constitutes the subject of the present invention, of separating phenolic compounds in salified form from an aqueous reaction mixture resulting from the reaction of a phenolic compound and glyoxylic acid in the presence of a base, leading to a reaction mixture comprising at least the excess of phenolic starting compound in salified form and the various mandelic compounds in salified form, resulting from the reaction, characterized in that said reaction mixture is contacted with a basic anion-exchange resin, leading to the selective attachment of the phenolic starting compound to said resin, and to the recovery of an aqueous stream comprising the mandelic compounds in salified form obtained from the reaction, and in that the phenolic compound in salified form that is attached to the resin is separated by a regenerative treatment of the resin.
• phenolic starting compound means a benzene compound in which at least one hydrogen atom directly bonded to the benzene nucleus is substituted by a hydroxyl group.
• the Applicant is citing the case of the separation of sodium guaiacolate from the aqueous mixture from condensation of sodium guaiacolate and glyoxylic acid.
• the method of the invention is not limited to the separation of this substrate, and is also suitable for phenolic starting compounds in salified form corresponding to the following formula:
• M is preferably sodium.
• alkyl groups include linear or branched alkyl groups having from 1 to 4 carbon atoms, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, and tert-butyl. Among these, the methyl and ethyl groups are preferred.
• linear or branched alkoxy groups having from 1 to 4 carbon atoms include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, and sec-butoxy groups. Methoxy and ethoxy groups are preferred.
• R also represents a halogen atom, preferably fluorine, chlorine, and bromine, and more preferably fluorine.
• Illustrative instances of compounds corresponding to the formula (I) include, more particularly, the salts of compounds selected from the group consisting of the following: phenol, guaiacol, 3-methoxyphenol, guaethol, 3-ethoxyphenol, 2-isopropoxyphenol, 3-isopropoxyphenol, 2-methoxy-5-methylphenol, 2-methoxy-6-methylphenol, 2-methoxy-6-tert-butylphenol, 3-chloro-5-methoxyphenol, 2,3-dimethoxy-5-methylphenol, 2,3-dimethoxyphenol, 2,6-dimethoxyphenol, 3,5-dimethoxyphenol, cresols, tert-butylphenol, 2-methoxyphenol, and 4-methoxyphenol.
• the preferred compounds of formula (I) are phenol, guaiacol, and guaethol.
• the method of the invention is applied to the aqueous reaction mixture obtained from the reaction of a phenolic compound in salified form of formula (I) and glyoxylic acid.
• the condensation reaction of the phenolic compound of formula (I) and glyoxylic acid may be conducted in the presence of an ammonium hydroxide, but more preferably in the presence of an alkali metal hydroxide, which may be sodium hydroxide or potassium hydroxide. For economic reasons it is preferred to select sodium hydroxide.
• glyoxylic acid an aqueous solution of glyoxylic acid is employed that has a concentration of, for example, between 15% and 70% by weight.
• the glyoxylic acid is reacted with the phenolic compound of formula (I) in excess.
• the molar ratio between the phenolic compound of formula (I) and the glyoxylic acid is between 1.1 and 4.0, preferably between 1.5 and 3.0.
• the alkali metal hydroxide solution employed has a concentration of generally between 10% and 50% by weight.
• the amount of alkali metal hydroxide introduced into the reaction mixture takes account of the amount needed in order to salify the hydroxyl function of the phenolic compound of formula (I), and the amount needed to salify the carboxyl function of the glyoxylic acid.
• the concentration of the phenolic compound of formula (I) is preferably between 0.5 and 1.5 mols/liter.
• the temperature of the reaction is selected advantageously between 20° C. and 60° C.
• the reaction is conducted at atmospheric pressure but under a controlled atmosphere of inert gases, preferably nitrogen or rare gases, especially argon. It is preferred to select nitrogen.
• inert gases preferably nitrogen or rare gases, especially argon. It is preferred to select nitrogen.
• the reaction mixture is maintained with stirring and at the temperature selected from the aforementioned range, for a variable duration of from 1 to 10 hours.
• an aqueous reaction mixture that comprises the excess of phenolic compound in salified form corresponding to the formula (I) and various mandelic compounds in salified form, denoted by the expression “mandelic compounds” and corresponding to the following formulae:
• the preferred mandelic compounds correspond to the formulae (IIa), (IIb) and (IIc), in which M represents a sodium atom, x is a number from 0 to 3, and preferably is 1, and the groups R, which are identical or different, represent an alkyl or alkoxy group having from 1 to 4 carbon atoms, preferably a methoxy or ethoxy group, or a halogen atom.
• the invention applies more particularly, in the context of the preparation of vanillin, to an aqueous mixture comprising sodium guaiacolate and mandelic compounds in salified form: 4-hydroxy-3-methoxymandelic acid, 2-hydroxy-3-methoxymandelic acid, 4-hydroxy-5-methoxy-1,3-dimandelic acid, in salified form.
• the invention is also applied preferably, for the preparation of ethylvanillin, to a reaction mixture which is an aqueous mixture comprising sodium guaetholate and mandelic compounds in salified form: 3-ethoxy-4-hydroxymandelic acid, 3-ethoxy-2-hydroxymandelic acid, 5-ethoxy-4-hydroxy-1,3-dimandelic acid, in salified form.
• the concentration by weight of the phenolic starting compound in salified form preferably sodium guaiacolate or sodium guaetholate, varies generally between 1% and 20% by weight, preferably between 5% and 10% by weight.
• the concentration by weight of mandelic compounds (o-, p-, and di-mandelate) in the reaction mixture is typically between 3% and 30% by weight, preferably between 5% and 20% by weight.
• the method of the invention for separating the phenolic compound in salified form is therefore implemented on the aqueous reaction mixture as defined above.
• the mixture therefore comprises sodium guaiacolate or sodium guaetholate and various reaction products, namely monofunctional or difunctional sodium mandelates as specified in accordance with formulae (IIa), (IIb), and (IIc), predominantly the compound of formula (IIb).
• the reaction mixture as described above is contacted with a basic resin, leading to the attachment to the resin of the phenolic compound in salified form, and to the recovery of an aqueous stream comprising the products of the reaction.
• reaction mixture to be treated is therefore contacted with a basic, preferably weakly basic, anion-exchange resin.
• the resins are polymeric structures which carry functional groups such as primary, secondary or tertiary amino or quaternary ammonium groups.
• the resins may comprise one or more functional groups corresponding to the following formulae:
• One very preferred group of resins very suitable for the method of the invention is composed of resins formed from a polystyrene backbone which carries basic functional groups as defined above.
• the polystyrene backbone is obtained by polymerizing styrene and divinylbenzene, under the influence of an activation catalyst, usually an organic peroxide, leading to a crosslinked polystyrene.
• an activation catalyst usually an organic peroxide
• the polymerization takes place usually in suspension, and produces beads or granules of polymer.
• these beads of crosslinked polystyrene are functionalized by treating them with chloromethyl ether in an anhydrous medium and in the presence of a catalyst (for example, AlCl 3 or SnCl 4 ), and then the chloromethylated polystyrene obtained, denoted as functionalized polymer P, is reacted with an amine or with ammonia, thereby allowing the chlorine of the chloromethyl group to be replaced by the basic functional group.
• a catalyst for example, AlCl 3 or SnCl 4
• the amine is advantageously a secondary or tertiary amine, and corresponds to the following formula:
• Resins considered weakly basic include resins which carry secondary amino (type —NHR a ) or tertiary amino (type —NR a R b ) functions.
• the commonest weakly basic resins are those which carry tertiary amine functions.
• the resulting resin carries a quaternary ammonium function —N + R a R b R c , which gives it a strongly basic character.
• the resins having a polystyrene backbone are employed preferably in the method of the invention.
• the invention does not rule out the use of resins having a backbone of some other kind, with the proviso that the backbone carries the appropriate basic groups.
• Beads are prepared from an acrylic ester and divinylbenzene, which are copolymerized in suspension in the presence of a free-radical activation catalyst.
• the acrylic polyester thus formed is reacted with a polyamine containing at least one primary amine function and one secondary or tertiary amine function.
• the primary amine function reacts with the ester function of the polymer, leading to an amide function, while the other amino-functional group as defined constitutes the active anion-exchange group.
• Numerous resins are commercially available products in dry or wet form. One or other of the forms may be used in the method of the invention.
• the resins in question may be gel resins or macroporous resins; the latter type of resins is preferred.
• the resins are typically present in the form of substantially spherical particles having a diameter of from 0.3 to 1.5 mm, preferably between 0.3 and 1.2 mm.
• the concentration of (basic) active sites on the resin is advantageously between 1 and 3 milliequivalents of active sites per liter of dry polymer, and, preferably, between 1.2 and 1.8 milliequivalents of active sites per liter of dry polymer.
• Amberjet 4400 and Amberlyst A26 and Dowex 22 are examples of strong basic resins which may be suitable.
• the preferred resins are the weakly basic resins, such as, more particularly, the following: Amberlyst A21, Amberlite IRA 67, Lewatit MP 64, Lewatit MP 62, and Purolite A100.
• the reaction mixture obtained at the end of the condensation reaction is passed over the anion-exchange resin.
• the stream is thus at a temperature close to the condensation temperature of between 20° C. and 60° C.
• the resin is placed in a stirred reactor or else in a column, the medium being introduced generally from top to bottom.
• the amount of resin employed is at least equal to the amount of phenolic compound in salified form that is to be recovered.
• an aqueous stream is recovered that comprises all of the mandelic compounds in salified form, while the phenolic compound in salified form, preferably sodium guaiacolate or sodium guaetholate, is attached to the resin.
• the aqueous stream comprising the mandelic compounds in salified form may be directly input into the oxidizing operation, thereby making it possible to obtain the aromatic aldehyde corresponding to the mandelic compounds in salified form.
• the phenolic compound in salified form is recovered by regeneration of the resin.
• Regeneration of the resin by means of a base is selected with preference.
• Suitable bases include, in particular, sodium hydroxide, aqueous ammonia, and sodium carbonate.
• a basic treatment is carried out, preferably using a basic aqueous solution, having a concentration of 2% to 10% by weight, and more preferably between 3% and 8% by weight.
• Sodium hydroxide is typically used.
• the amount of base employed is at least equal to the amount of phenolic compound in salified form that is to be regenerated.
• the method of the invention makes it possible to separate an aqueous stream comprising the various mandelic compounds in salified form.
• the method of the invention allows access to hydroxyaromatic aldehydes corresponding to the formulae (IIa), (IIb), and (IIc) in which the glycol group of formula —CHOH—COOH is replaced by a formyl group CHO.
• the oxidation reaction may be conducted according to the techniques that are described in the literature. Thus it is possible to use the catalysts that are conventionally used in oxidation reactions of mandelic compounds in a basic medium.
• the oxidation is generally conducted by oxygen or air under pressure, in the presence of an appropriate catalyst such as, for example, derivatives of chromium, manganese, iron, cobalt, nickel, copper, zinc, bismuth, aluminum, silver, vanadium or osmium.
• an appropriate catalyst such as, for example, derivatives of chromium, manganese, iron, cobalt, nickel, copper, zinc, bismuth, aluminum, silver, vanadium or osmium.
• a catalyst comprising at least two metallic elements.
• the invention allows easy access to hydroxybenzaldehydes, and more particularly to vanillin and its analogs, for example, 3-ethylvanillin and 3-isopropylvanillin, by oxidation, respectively, of p-hydroxymandelic acid and of 4-hydroxy-3-methoxymandelic acid, 3-ethoxy-4-hydroxymandelic acid, or 4-hydroxy-3-isopropoxymandelic acid.
• the selectivity of the reaction is defined as the following ratio: [guaiacol]attached/([guaiacol]attached+[mandelate]attached).
• the resin used is an Amberlyst A21 resin, which is a weakly basic anion-exchange resin functionalized with tertiary amines.
• the average diameter is defined as being such that 50% by weight of the beads have a diameter greater than or less than the average diameter.
• a Schott tube is charged with 36.70 g of a stream comprising 2.14 g of sodium guaiacolate (0.014 mol) and 2.54 g of sodium p-mandelate (0.013 mol) of formula:
• the ratio defining the selectivity is 1.
• Lewatit MP64 resin is employed, which is a weakly basic anion-exchange resin based on a styrene-divinylbenzene copolymer having a macroporous structure and containing tertiary/quaternary ammonium functional groups.
• Example 1 is repeated, with the only difference that the nature of the resin is changed.
• Amberlite IRA 67 resin is employed, which is a weakly basic anion-exchange resin having an acrylic gel matrix functionalized with tertiary amines.
• Example 1 is repeated, with the only difference that the nature of the resin is changed.
• the resin employed is Purolite A100, which is a weakly basic anion-exchange resin having a polystyrene matrix functionalized with tertiary amines.
• the resin takes the form of beads with an average diameter of between 0.6 and 0.85 mm.
• the resin is employed in a 300 ml column with a diameter of 2.8 cm and a height of 24 cm.
• the volume of the resin is 150 ml.
• the column is maintained under atmospheric pressure at 35° C.
• This resin is percolated at a rate of 1.5 m/h with a stream comprising 5.2% of sodium guaiacolate and 5.9% of mandelic compounds in sodium salt form (o-, p-, and di-mandelate), obtained from a condensation reaction between glyoxylic acid and guaiacol, in the presence of sodium hydroxide, conducted according to the teaching of the prior art (WO 99/65853), and corresponding to the formulae (IIa), (IIb) and (IIc) in which R represents a methoxy group, x is 1, and M is sodium.
• the ratio which defines the selectivity is 1.
• the sodium guaiacolate attached to the resin is recovered by treatment with sodium hydroxide.
• a 5% by weight aqueous solution of sodium hydroxide is percolated through the resin at a rate of 2 m/s.
• a stream is recovered which contains sodium guaiacolate with a yield of 88% by weight, the yield being defined as the weight ratio (in %) between the guaiacolate introduced and the guaiacolate recovered.
• This guaiacolate may be directly recycled to the condensation step.
• the stream at the column outlet that contains the mandelic compounds in salified form is then oxidized without further addition of aqueous sodium hydroxide solution.
• the stream is charged to a 316L stainless-steel reactor equipped with mechanical stirring, baffles, and an air inlet.
• This reaction mixture is admixed with a catalyst system comprising CoCl 2 .6H 2 O and CuSO 4 .5H 2 O, which are employed, respectively, in an amount, expressed as molar percentage of mandelic compounds, of 0.125 and 0.125.
• a catalyst system comprising CoCl 2 .6H 2 O and CuSO 4 .5H 2 O, which are employed, respectively, in an amount, expressed as molar percentage of mandelic compounds, of 0.125 and 0.125.
• the mixture is subsequently heated to 80° C. and air is introduced at a rate of 1.6 L/h.
• Example 4 is reproduced, with the sole difference that the reaction mixture percolated results from the reaction of guaethol and glyoxylic acid in the presence of sodium hydroxide, and therefore comprises sodium guaetholate and the mandelic compounds in sodium salt form (o-, p-, and di-mandelate) which correspond to the formulae (IIa), (IIb), and (IIc) in which R represents an ethoxy group, x is 1, and M is sodium.

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• 2008
  • 2008-05-22 FR FR0802784A patent/FR2931476B1/fr not_active Expired - Fee Related
• 2009
  • 2009-05-15 WO PCT/EP2009/055934 patent/WO2009141280A1/fr active Application Filing
  • 2009-05-15 US US12/992,838 patent/US20110230674A1/en not_active Abandoned
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  • 2009-05-15 CN CN200980118600.5A patent/CN102036942B/zh not_active Expired - Fee Related
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