Patent Application
20090001322
The present invention relates to a process for preparing alkoxypolyoxyalkylene (meth)acrylates, and to a stabilizer mixture which is particularly appropriate for this process.
DE 10 2004 042799 (BASF) describes the preparation of polyethylene glycol (meth)acrylates with catalysis by catalysts which, at 90 degrees Celsius, have a solubility in polyethylene glycol of not more than 10 g/litre. The catalysts used are hydroxides, oxides, carbonates or hydrogen carbonates of mono- or divalent alkali metals or alkaline earth metals.
Alkoxypolyoxyalkylene (meth)acrylates are already known and are proposed, for example, in the Patent Application EP 0 965 605 A2 (NOF Corporation) for the preparation of dispersants. The alkoxypolyoxyalkylene (meth)acrylates are prepared by adding a catalyst, for example p-toluenesulphonic acid monohydrate, to a polyoxyalkylene monoalkyl ether and subsequently performing an esterification with acrylic acid or methacrylic acid, by adding a catalyst, for example sodium methoxide, to a polyoxyalkylene monoalkyl ether and subsequently transesterifying with an alkyl acrylate, for example methyl acrylate, or with an alkyl methacrylate, for example methyl methacrylate, by reacting a polyoxyalkylene monoalkyl ether with acryloyl chloride or methacryloyl chloride, or by reacting a polyoxyalkylene monoalkyl ether with acrylic anhydride or methacrylic anhydride.
In EP 0 965 605 A2, Examples 7-11 and Comparative Examples 3 and 4 illustrate the preparation routes. In Examples 7, 9-11 and Comparative Examples 3 and 4, an alkoxide, for example sodium methoxide, is initially charged, reacted with an alkylene oxide, for example ethylene oxide, propylene oxide or an alkylene oxide mixture of propylene oxide and 1,2-butylene oxide, neutralized with hydrochloric acid and then esterified with acrylic acid or methacrylic acid in toluene with catalysis by p-toluenesulphonic acid. The stabilizer used is hydroquinone.
In Example 8 of the abovementioned application, sodium methoxide is reacted with ethylene oxide in methanol and neutralized with hydrochloric acid, and the product is isolated and dried, admixed again with sodium methoxide in methanol and transesterified with methyl methacrylate. The stabilizer added is t-butylhydroxy-toluene.
Even though the processes described above are suitable in principle for preparing alkoxypolyoxyalkylene (meth)acrylates, more efficient and less expensive routes to the preparation are nevertheless desirable.
It is therefore an object of the present invention to specify an improved process for preparing alkoxypolyoxyalkylene (meth)acrylates. This process should enable the preparation of the alkoxypolyoxyalkylene (meth)acrylates in a particularly simple manner, on the industrial scale and inexpensively, in high quality and with acceptable reaction rates.
In the text which follows, the term (meth)acrylates means both acrylates and methacrylates, and also mixtures of the two compounds.
It has been found, surprisingly, that this object can be achieved by a process in which a reactor
The inventive procedure allows a “one-pot synthesis”, i.e. an isolation and purification of intermediates is no longer required.
The present invention therefore relates to a process for preparing poly(oxyalkylene) monoacrylic esters and monomethacrylic esters by reacting acrylic anhydride or methacrylic anhydride (hereinafter (meth)acrylic anhydride A) with a reaction product formed from
wherein the end product, after the reaction has ended, is optionally admixed with water, and the methacrylic anhydride is used in a molar ratio, based on the reaction product of the metal alkoxide MetOR10, the alcohol R12OH and the alkylene oxide of the formula (VI), which is between 1:1 and 3:1.
The process according to the invention is associated with a series of advantages. Firstly, separate provision of monofunctional polyoxyalkylene raw materials bearing OH groups is no longer necessary, and, secondly, shorter reaction times are achieved overall than in the method in two separate reactions, which is the current state of the art.
In addition, improved means of stabilizing the reaction mixture and the resulting product were to be indicated.
It has been found that, surprisingly, suitable selection of the stabilizers or of the stabilizer mixture, especially those which are water-soluble and unreactive toward methacrylic anhydride, considerably prolongs the stability time of the monomer.
This object and further objects which have not been described specifically but which can be discerned from the above-described connections are achieved by a process for preparing alkoxypolyoxyalkylene (meth)acrylates having all features of the present independent process claims. The dependent process claims describe particularly advantageous procedures for preparing alkoxypolyoxyalkylene (meth)acrylates. Further product claims protect a stabilizer mixture whose use in the present process is very particularly appropriate.
In the process according to the invention, at least one metal alkoxide MetOR10 is first initially charged. The Met radical is lithium, sodium, potassium, rubidium or caesium, preferably lithium, sodium or potassium, in particular sodium or potassium, more preferably sodium. It is also possible for a metal hydroxide to be initially charged, in which case dewatering of the reaction solution before the addition of the alkylene oxide is required.
R10 is a linear or branched alkyl radical, preferably having 1 to 18 carbon atoms, especially a methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl or an octadecyl radical. R10 may also be hydrogen.
Particular preference is given to a radical which has 1 to 4 carbon atoms.
R12 is a linear or branched, optionally alkoxylated alkyl radical, preferably having 1 to 18 carbon atoms, in particular a methyl, 2-methoxyethyl, 2-(2-methoxyethoxy)ethyl, 2-(2-(2-methoxyethoxy)ethoxy)-ethyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl or an octadecyl radical, where the molar mass of R12 is less than the molar mass of the inventive alkoxypolyoxyalkylenes. Particular preference is given to a radical which has 1 to 4 carbon atoms.
In the process according to the invention, at least one alkylene oxide of the formula (VI) is then added and it is reacted with the metal alkoxide.
The R11 radicals are each independently hydrogen or a linear or branched alkyl radical, preferably having 1 to 8 carbon atoms, especially a methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl or an n-octyl radical. A radical which has 1 to 4 carbon atoms is particularly preferred.
In this context, ethylene oxide, propylene oxide and 1,2-butylene oxide, and also mixtures of these compounds, have been found to be very particularly useful.
The reaction of the metal alkoxide with the alkylene oxide is preferably performed in a reactive solvent R12OH. A particularly favourable solvent is the alcohol whose alkoxide is reacted with the alkylene oxide.
The length of the polyalkylene block can be adjusted via the molar ratio of metal alkoxide and alcohol R12OH on the one hand to alkylene oxide on the other. It is preferably in the range of 1:1-10 000, appropriately in the range of 1:1-1000, especially in the range of 1:1-100.
The reaction is appropriately performed at a temperature in the range of 60° C. to 150° C., preferably in the range of 80° C. to 120° C., especially in the range of 90° C. to 110° C.
The reaction time is preferably in the range of 1 to 20 hours, preferably in the range of 2 to 10 hours, especially in the range of 4 to 8 hours.
After the reaction, any excess alkylene oxide can be removed, for example by applying a reduced pressure.
The reaction product from the reaction of the metal alkoxide and alcohol with the alkylene oxide is reacted directly with (meth)acrylic anhydride, i.e. without isolating and/or purifying the intermediate. The expression (meth)acrylic anhydride encompasses both methacrylic anhydride and acrylic anhydride, and also mixtures of the two compounds.
In the context of the present invention, the (meth)acrylic anhydride, based on the sum of the metal alkoxide and the alcohol, is preferably used in excess, preferably in a molar ratio of (meth)acrylic anhydride to metal alkoxide of greater than 1, especially in the range of 1-3:1.
The reaction is appropriately performed at a temperature in the range of 60° C. to 150° C., preferably in the range of 70° C. to 110° C., especially in the range of 80° C. to 100° C.
The reaction time is preferably in the range of 1 to 20 hours, preferentially in the range of 2 to 10 hours, especially in the range of 4 to 8 hours.
The Stabilizers and the Stabilizer Mixtures
In addition, the reaction is appropriately performed in the presence of at least one stabilizer or one stabilizer mixture. In the context of the present invention, stabilizers (antioxidants) denote preferably organic compounds which are intended to prevent undesired polymerization of the methacrylic anhydride and/or of the alkoxypolyoxyalkylene (meth)acrylate. The action of the stabilizers usually consists in acting as free-radical scavengers for the free radicals which occur in the polymerization. For further details, reference is made to the common technical literature, especially to the Römpp-Lexikon Chemie; Editors: J. Falbe, M. Regitz; Stuttgart, New York; 10th edition (1996); under “Antioxidants”, and the literature references cited at this point.
Stabilizers particularly suitable for the purposes of the present invention include tocopherol, tert-butylmethoxyphenol (BHA), butylhydroxytoluene (BHT), octyl gallate, dodecyl gallate, ascorbic acid, optionally substituted phenols, optionally substituted hydroquinones, for example hydroquinone monomethyl ether (HQME), optionally substituted quinones, optionally substituted pyrocatechols, optionally substituted aromatic amines, optionally substituted metal complexes of an aromatic amine, optionally substituted triazines, organic sulphides, organic polysulphides, organic dithiocarbamates, organic phosphites and organic phosphonates.
Optionally substituted phenols are used with very particular preference in accordance with the invention. These preferably satisfy the formula (I)
where the R1 radicals are each independently hydrogen, a linear or branched alkyl radical, preferably having 1 to 8 carbon atoms, especially a methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl or an n-octyl radical, which favourably has 1 to 4 carbon atoms, an optionally substituted cycloalkyl radical, preferably having 4 to 8 carbon atoms, especially a cyclohexyl radical, an optionally substituted aryl radical, preferably having 6 to 18 carbon atoms, or a halogen, preferably fluorine, chlorine or bromine, and where R2 is a linear or branched alkyl radical, preferably having 1 to 8 carbon atoms, especially a methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl or is an n-octyl radical, which more preferably has 1 to 4 carbon atoms, is an optionally substituted cycloalkyl radical, preferably having 4 to 8 carbon atoms, especially a cyclohexyl radical, or is an optionally substituted aryl radical, preferably having 6 to 18 carbon atoms.
Compounds (I) which are very particularly favourable in this context have hydrogen as R1. R2 is preferably an alkyl radical having 1 to 4 carbon atoms, especially a methyl radical.
It has also been found that compounds of the formula (II) are particularly useful for the purposes of the present invention
where the R3, R4 and R5 radicals are each independently hydrogen, a linear or branched alkyl radical, preferably having 1 to 8 carbon atoms, especially a methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl or an n-octyl radical, which more preferably has 1 to 4 carbon atoms, an optionally substituted cycloalkyl radical, preferably having 4 to 8 carbon atoms, especially a cyclohexyl radical, an optionally substituted aryl radical, preferably having 6 to 18 carbon atoms, a halogen, preferably fluorine, chlorine or bromine, or a radical of the formula (III)
in which R6 is a linear or branched alkyl radical having 1 to 6 carbon atoms, preferably a methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl or n-hexyl radical, especially an ethyl radical.
Compounds (II) which are very particularly favourable in this context have hydrogen as R4. R3 is preferably an alkyl radical having 1 to 4 carbon atoms, especially a methyl radical. R5 is appropriately an alkyl radical having 1 to 4 carbon atoms, especially a tert-butyl radical.
For the purposes of the present invention, compounds of the formula (IIa) have also been found to be suitable.
The compound of the formula (IIb) has also been found to be particularly favourable:
where: R5=tert-butyl.
The compound is sold under the brand Topanol® A by Ciba.
In addition, favourable results can also be achieved using compounds of the formula (IV)
where o is an integer in the range of 1 to 4 and p is 1 or 2, preferably 2,
A particularly preferred compound of the formula (IV) is glycol bis[3,3-bis(4′-hydroxy-3′-tert-butylphenyl)-butanoate].
In a very particularly preferred embodiment of the present invention, a stabilizer mixture is used which comprises
where the R9 radicals are each independently a linear or branched alkyl radical, preferably having 1 to 6, especially having 1 to 4, carbon atoms, such as a methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl or a tert-butyl radical, especially a methyl radical. The compound of the formula (V) is sold under the brand Tempol® by Ciba and under the name 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl by Degussa GmbH.
The weight ratio of the compound (I) to the compound (II) or (IV) and to the compound (V) is preferably in the range of 1:0.1-25.0:0.01-1.0.
Based on the (meth)acrylic anhydride, the proportion of the stabilizers individually or as a mixture is preferably 0.001 to 2.0% by weight.
Owing to the hydrolysis sensitivity of the reactants, it is appropriate to work under substantially anhydrous conditions. Moreover, the reactants used are dried substantially completely. In addition, the use of an inert gas atmosphere, especially of dry nitrogen and/or argon in the performance of the alkoxylation step has also been found to be very particularly useful. In the subsequent reaction with (meth)acrylic anhydride, in contrast, oxygen should be present, either in a mixture with the inert gases mentioned or as a dry air atmosphere, in order to increase the stabilization against polymerization.
Possible fields of use of the alkoxypolyoxyalkylene (meth)acrylates are already known. They are suitable, inter alia, for preparing dispersants.
The invention will be illustrated in more detail hereinafter by several inventive examples, without any intention that it be restricted to these specific embodiments.
The length of the polyalkylene block was determined by withdrawing a small sample after step b) and determining the OH number.
Apparatus: 2 l Büchi jacketed glass autoclave with manometer, mechanical stirrer, internal Pt 100 temperature sensor, inlet tube and oil circulation thermostat.
The reactor is evacuated, filled with nitrogen and charged with 6.6 g of a 30% solution of sodium methoxide in methanol (NM 30, Degussa AG) . 6 g of dry methanol are added and the mixture is heated to 100° C., and 756 g of ethylene oxide are pumped in within 2 h, such that a pressure of 6 bar is not exceeded. Thereafter, reaction is allowed to continue at this temperature for a further 0.5 h. The mixture is cooled to 80° C. and unconsumed ethylene oxide is drawn off under reduced pressure (approx. 150 mbar) (time: approx. 0.5 h). A sample (10 g) is withdrawn for hydroxyl number determination, and 83.6 g of methacrylic anhydride which contain 3.4 g of hydroquinone monomethyl ether (HQME) and 0.17 g of 2,6-dimethyl-4-tert-butylphenol (Topanol® A) and 0.08 g of 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (Tempol®) in dissolved form are added to the reactor, and the mixture is heated at standard pressure with slow introduction of air to 90° C. for 6 h.
After cooling to room temperature, the reaction product is withdrawn, weighed and admixed with the same amount of water. 1700 g of an aqueous methacrylic acid-containing methoxypolyethylene glycol 2000 methacrylate solution are obtained.
OH number of the 10 g sample consisting of methoxypolyethylene glycol 2000: 27 mg KOH/g
M=(molar mass of potassium hydroxide)*100/(OH number)=5600/27=2074
The content of HQME has declined compared to the initial weight (2000 ppm based on aqueous product solution) as a result of side reactions, as has the Tempol content (initial weight 47 ppm based on aqueous product solution) . Compared to this, the content of Topanol A is reduced only from 100 ppm to 80 ppm.
As Example 1, except with use of 2.64 g of NM30 solution and 12.3 g of methyltriglycol instead of the methanol. Reaction is effected with 605 g of ethylene oxide in 1.5 h. After the sampling, 28 g of methacrylic anhydride which contains 2.5 g of HQME, 0.06 g of Tempol and 0.06 g of Topanol® A in dissolved form are added. After the reaction and water addition have ended, 1270 g of aqueous methoxypolyethylene glycol 5000 methacrylate solution are obtained.
OH number of the 10 g sample, consisting of methoxypolyethylene glycol 5000: 11 mg KOH/g
As Example 1, except with use of 13.2 g of NM30 solution and 12 g of methanol. Reaction is effected with 737 g of ethylene oxide in 2 h. After the sampling, 174 g of methacrylic anhydride which contains 3.7 g of HQME, 0.09 g of Tempol and 0.35 g of Topanol® A in dissolved form are added. After the reaction and water addition have ended, 1880 g of aqueous methoxypolyethylene glycol 1000 methacrylate solution are obtained.
OH number of the 10 g sample, consisting of methoxypolyethylene glycol 1000: 55 mg KOH/g
As Example 1, except with use of 18 g of NM30 solution and 16.5 g of methanol. Reaction is effected with 760 g of ethylene oxide in 2 h. After the sampling, 242 g of methacrylic anhydride which contains 4.2 g of HQME, 0.1 g of Tempol® and 0.5 g of Topanol® A in dissolved form are added. After the reaction and water addition have ended, 2080 g of aqueous methacrylic acid-containing methoxypolyethylene glycol 750 methacrylate solution are obtained.
OH number of the 10 g sample, consisting of methoxypolyethylene glycol 750: 75 mg KOH/g
As Example 1, except with use of 26.4 g of NM30 solution and 24 g of methanol. Reaction is effected with 737 g of ethylene oxide in 2 h. After the sampling, 359 g of methacrylic anhydride which contains 4.6 g of HQME, 0.1 g of Tempol® and 0.72 g of Topanol® A in dissolved form are added. After the reaction and water addition have ended, 2300 g of aqueous methacrylic acid-containing methoxypolyethylene glycol 500 methacrylate solution are obtained.
OH number of the 10 g sample, consisting of methoxypolyethylene glycol 500: 110 mg KOH/g
As Example 1, except with use of 39.6 g of NM30 solution and 36 g of methanol. Reaction is effected with 774 g of ethylene oxide in 2.5 h. After the sampling, 554 g of methacrylic anhydride which contains 5.6 g of HQME, 0.14 g of Tempol® and 1.11 g of Topanol® A in dissolved form are added. After the reaction and water addition have ended, 2800 g of aqueous methacrylic acid-containing methoxypolyethylene glycol 350 methacrylate solution are obtained.
OH number of the 10 g sample, consisting of methoxypolyethylene glycol 350: 155 mg KOH/g
As Example 1, except that, after the sampling, 70 g of acrylic anhydride which contains 3.3 g of HQME, 0.08 g of Tempol® and 0.14 g of Topanol® A in dissolved form are added. After the reaction and water addition have ended, 1600 g of aqueous acrylic acid-containing methoxypolyethylene glycol 2000 acrylate solution are obtained.
OH number of the 10 g sample, consisting of methoxypolyethylene glycol 2000: 26 mg KOH/g
As Example 1, except that, instead of the sodium methoxide solution and the methanol, 4.1 g of potassium tert-butoxide and 27 g of dry n-butanol are used. Reaction is effected with 971 g of propylene oxide in 4 h. After the sampling, 115 g of methacrylic anhydride which contains 4.5 g of HQME, 0.11 g of Tempol® and 0.23 g of Topanol® A in dissolved form are added. After the reaction and water addition have ended, 2200 g of aqueous methacrylic acid-containing butoxypolypropylene glycol 2000 methacrylate solution are obtained.
OH number of the 10 g sample, consisting of butoxypolypropylene glycol 2000: 25 mg KOH/g
As Example 8, except that reaction is effected successively with 486 g of ethylene oxide and 486 g of propylene oxide in a total of 4 h. After the sampling, 115 g of methacrylic anhydride which contains 4.5 g of HQME, 0.11 g of Tempol® and 0.23 g of Topanol® A in dissolved form are added. After the reaction and water addition have ended, 2200 g of aqueous methacrylic acid-containing butoxypolyethylene polypropylene glycol 2000 methacrylate solution are obtained.
OH number of the 10 g sample, consisting of butoxy-polyethylene polypropylene glycol 2000: 28 mg KOH/g
As Example 1, except using 18 g of NM30 solution and 261 g of C16-18 alcohol (Hydrenol® D, Cognis). At 100° C./150 mbar, the methanol fraction is drawn off, then the mixture is blanketed with nitrogen and reacted with 1100 g of ethylene oxide. After the sampling, 229 g of methacrylic anhydride which contains 6.3 g of HQME, 0.16 g of Tempol® and 0.46 g of Topanol® A in dissolved form are added. After the reaction and water addition have ended, 3190 g of aqueous methacrylic acid-containing alkoxypolyethylene glycol 1100 methacrylate solution are obtained.
OH number of the 10 g sample, consisting of C16-18 alkoxypolyethylene glycol methacrylate 1100: 50 mg KOH/g
Separate ethoxylation and methacrylation according to the prior art
Apparatus: 2 l Büchi jacketed glass autoclave with manometer, mechanical stirrer, internal Pt 100 temperature sensor, inlet tube and oil circulation thermostat.
The reactor is evacuated, filled with nitrogen and charged with 6.6 g of a 30% solution of sodium methoxide in methanol (NM 30, Degussa AG) . Another 6 g of dry methanol are added, the mixture is heated to 100° C. and 756 g of ethylene oxide are pumped in within 2 h, such that a pressure of 6 bar is not exceeded. Thereafter, the reaction is allowed to continue at this temperature for a further 0.5 h. The mixture is cooled to 80° C. and unconsumed ethylene oxide is drawn off under reduced pressure (approx. 150 mbar) (duration: approx. 0.5 h). The methoxypolyethylene glycol 2000 formed is withdrawn via the bottom valve and a sample (10 g) is taken for hydroxyl number determination. Yield: 753 g (98% of theory)
OH number of the 10 g sample, consisting of methoxy-polyethylene glycol 2000: 28 mg KOH/g
The product is introduced into a 2 l round-bottomed flask with stirrer and reflux condenser with 83.6 g of methacrylic anhydride which comprises 3.4 g of hydroquinone monomethyl ether (HQME) and 0.17 g of 2,6-dimethyl-4-tert-butylphenol (Topanol® A) and 0.08 g of 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (Tempol®) in dissolved form, and heated to 90° C. at standard pressure while passing air through slowly. After 6 h, a sample is taken and, according to NMR spectroscopy, has a conversion of 90%. After a total of 8 h at 90° C., the mixture is cooled to room temperature, and the reaction product is withdrawn, weighed and admixed with the same amount of water. 1650 g of an aqueous methacrylic acid-containing methoxypolyethylene glycol 2000 methacrylate solution are obtained.
As Example 1, except using 1.44 g of sodium hydroxide and 60 g of triethylene glycol monomethyl ether. After heating to 100° C., water of reaction formed is drawn off under reduced pressure for 0.5 h. 624 g of ethylene oxide are then pumped in within 1.5 h. After the sampling, 83.6 g of methacrylic anhydride which contains 3.4 g of hydroquinone monomethyl ether (HQME) and 0.17 g of 2,6-dimethyl-4-tert-butylphenol (Topanol® A) and 0.08 g of 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (Tempol®) in dissolved form are introduced into the reactor at standard pressure while slowly passing air through at 90° C. for 6 h.
After cooling to room temperature, the reaction product is withdrawn, weighed and admixed with the same amount of water. 1500 g of an aqueous methacrylic acid-containing methoxypolyethylene glycol 2000 methacrylate solution are obtained.
OH number of the 10 g sample consisting of methoxy-polyethylene glycol 2000: 29 mg KOH/g
As Example 1, except that the stabilizer added to the methacrylic anhydride is only 3.4 g of Topanol A®. The resulting 1680 g of a methoxypolyethylene glycol 2000 methacrylate solution in water contain 1520 ppm of Topanol A®, i.e. of the 2000 ppm of stabilizer used, only a small portion has been consumed by side reactions.
As Example 1, except that the stabilizer added to the methacrylic anhydride is only 0.85 g of phenothiazine (500 ppm based on aqueous product solution). The resulting 1690 g of a methoxypolyethylene glycol 2000 methacrylate solution in water contain 490 ppm of phenothiazine (determined by liquid chromatography). After 1 week of storage in diffuse daylight, the product solution has polymer fractions (determined by NMR spectroscopy).
As Example 1, except that the stabilizer added to the methacrylic anhydride is 0.85 g of 2,6-di(tert-butyl)-4-methylphenol (Topanol O®) (500 ppm based on aqueous product solution). The resulting 1700 g of a methoxypolyethylene glycol 2000 methacrylate solution in water contain 480 ppm of Topanol O® (determined by liquid chromatography) . The product solution is stable but is cloudy.
As Example 1, except that the stabilizer added to the methacrylic anhydride is 0.85 g of Tempol® (500 ppm based on aqueous product solution). The resulting methoxypolyethylene glycol 2000 methacrylate solution in water contains 50 mol % of polymer (determined by NMR spectroscopy).
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2006 008 998.7 | Feb 2006 | DE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP07/50875 | 1/30/2007 | WO | 00 | 7/2/2008 |
