Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing
Reexamination Certificate
1999-10-25
2001-05-29
Siegel, Alan (Department: 1625)
Organic compounds -- part of the class 532-570 series
Organic compounds
Oxygen containing
C568S618000
Reexamination Certificate
active
06239315
ABSTRACT:
The present invention relates to an improved process for preparing glycol monoethers from olefins. The invention further relates to a catalyst mixture which is used in the process of the present invention.
Glycol monoethers are widely used industrially as solvents, absorption liquids in gas scrubbing, antifreezes, hydraulic fluids, lubricants, plasticizers, surfactants, precursors for fiber products such as polyesters or urethanes, additives for printing inks and in cosmetic and skincare products.
The most important products are the corresponding glycol ethers of ethylene and propene. These glycol ethers are usually prepared by reacting epoxides of the parent olefins with the corresponding alcohols.
A disadvantage of this procedure is that a multi-stage process is required which involves initial preparation of the epoxides from the olefins followed by ring-opening reaction of the epoxides with alcohols at a higher temperature using, for example, sulfuric acid.
It is an object of the present invention to provide a simpler process for preparing glycol monoethers.
We have found that, surprisingly, this object is achieved and the above-described disadvantages are overcome by a simple single-stage synthesis which involves reacting olefins with a conventional epoxidizing reagent over suitable epoxidation catalyts and simultaneously allowing the presence of hydroxyl-containing organic compounds, such as alcohols, and acidic or basic alkoxylation catalysts. The epoxide intermediates are reacted in situ over the added alkoxylation catalysts to give glycol monoethers.
The present invention accordingly provides a process for preparing glycol monoethers from olefins, which comprises reacting the olefins with an epoxidizing reagent in the simultaneous presence of hydroxyl-containing organic compounds over a mixture of epoxidation catalysts and alkoxylation catalysts.
Preferred epoxidation catalysts in the catalyst mixture are titanium-containing silicates or titanium-, vanadium-, germanium- or tin-containing zeolites, in particualr titanium or vanadium silicalites having a zeolite structure assigned by X-ray diffraction to the MFI, MEL, BEA, MTW, TON, PER or MFI/MEL mixed structure. Such epoxidation catalysts are described, for example, in DE-A 44 25 672. According to DE-A 44 25 672, the abovementioned titanium or vanadium silicalites may contain noble metals such as platinum metals in amounts of 0.01-20% by weight, which is particularly advantageous when the epoxidizing reagent used is a hydrogen/oxygen mixture.
Preferred alkoxylation catalysts in the catalyst mixture are acidic catalysts in the form of mineral acids or in the form of solid acidic heterogeneous catalysts, and solid basic catalysts.
Examples of mineral acids are sulfuric acid, hydrochloric acid and orthophosphoric acid; for the purposes of the present invention, mineral acids include sufficiently acidic organic sulfonic acids and carboxylic acids such as p-toluenesulfonic acid, methanesulfonic acid or trifluoroacetic acid.
Solid alkoxylation catalysts are particularly suitable, i.e. those which do not dissolve in the reaction medium and which are present as solid phase (as heterogeneous catalysts) during the reaction.
Preference is given to solid acidic heterogeneous catalysts based on supported mineral acids, polymeric acidic ion exchange resins, composites of acidic ion exchange resins in inorganic materials, acidic metal oxides or acid zeolites. Examples of such heterogeneous catalysts are K10-type acidic sheet silicates, acidic metal oxides as described by Arata in Appl. Catalysis A: General 146 (1996), 3-32, and acidic zeolites of the structure type MFI (for example H-ZSM-5 zeolite), MEL, MFI/MEL, BEA (for example H-B-&bgr;-zeolite), MOR, FER, NES, ERI, OFF, MAZ, FAU, TON, CHA, RUT, BOG, LTA, NON, MTN, HEU, AFI, MTW, DOE, EUO, MTT, RHO, CAN, LTL, GIS, GME, VFI, EMT, DDR, SGT, CON, ZON or MFS.
Preference is furthermore given to solid basic catalysts based on alkali metal or alkaline earth metal oxides or hydroxides, supported bases, polymeric basic ion exchange resins, dendrimeric amines, talcites or hydrotalcites.
The above-described catalyst mixture usually comprises from 1 to 99 parts by weight of epoxidation catalysts and from 99 to 1 parts by weight of alkoxylation catalyts, when the latter are present in solid form, i.e. as heterogeneous catalysts. Preferred ranges for the proportions of these two types of catalyst are 5-95 parts by weight/95-5 parts by weight and in particular 20-80 parts by weight: 80-20 parts by weight. The above-described catalyst mixture may additionally comprise further conventional auxiliaries. When free mineral acids are present as alkoxylation catalysts, the proportion of epoxidation catalysts to alkoxylation catalysts is usually 90-99.999 parts by weight: 10-0.001 parts by weight, in particular 99-99.99 parts by weight: 1-0.01 parts by weight.
Since the above-described mixture of the solid epoxidation catalysts and the solid alkoxylation catalysts is novel, the present invention also provides a catalyst mixture for the single-stage epoxidation and alkoxylation of olefins, consisting of from 1 to 99 parts by weight of epoxidation catalysts and from 99 to 1 part by weight of solid alkoxylation catalysts.
Particularly useful epoxidizing reagents for the process of the present invention are aqueous hydrogen peroxide or a hydrogen/oxygen mixture. The use of hydrogen/oxygen mixtures for epoxidation is described, for example, in DE-A 44 25 672. However, organic peracids or hydroperoxides are also useful as epoxidizing reagents.
Hydroxyl-containing organic compounds are in principle any mono- and polyhydroxy compounds having sufficient O—H acidity. Preference is given to linear or branched C
1
- to C
20
-alkanols, C
5
- to C
8
-cycloalkanols and C
7
- to C
20
-arylalkanols. Examples of such alcohols are methanol, ethanol, propanol, isopropanol, butanol, isobutanol, sec-butanol, tert-butanol, pentanol, isopentanol, sec-pentanol, tert-pentanol, neopentanol, hexanol, heptanol, octanol, 2-ethylhexanol, nonanol, isononanol, decanol, undecanol, dodecanol, tridecanol, isotridecanol, tetradecanol, pentadecanol, hexadecanol, heptadecanol, octadecanol, eicosanol, cyclopentanol, cyclohexanol, cycloheptanol, cyclooctanol, benzyl alcohol, 2-phenylethanol, 3-phenylpropanol and 4-phenylbutanol. It is also possible to use mixtures of the abovementioned alcohols. Very particular preference is given to C
1
- to C
8
-alkanols.
The hydroxyl-containing organic compounds are used in stoichiometric amounts or in excess, based on the ethylenically unsaturated double bond equivalents of the olefin, and also as solvent. If the hydroxyl-containing compounds also react with additional functional groups in the olefins, the amount of hydroxyl-containing compounds has to be increased accordingly.
The olefin used can be any organic compound which contains at least one ethylenically unsaturated double bond. It may be aliphatic, aromatic or cycloaliphatic and may consist of a linear or branched structure. The olefin is preferably of from 2 to 30 carbon atoms. More than one ethylenically unsaturated double bond may be present, for example in dienes or trienes. The olefin may additionally contain functional groups, such as halogen atoms, carboxyl groups, carboxylic ester functions, hydroxyl groups, ether bridges, sulfide bridges, carbonyl functions, cyano groups, nitro groups or amino groups.
Typical examples of such olefins are ethylene, propene, 1-butene, cis- and trans-2-butene, 1,3-butadiene, pentenes, isoprene, hexenes, octenes, nonenes, decenes, undecenes, dodecenes, cyclopentene, cyclohexene, dicyclopentadiene, methylenecyclopropane, vinylcyclohexane, vinylcyclohexene, allyl chloride, acrylic acid, methacrylic acid, crotonic acid, vinylacetic acid, allyl alcohol, alkyl acrylates, alkyl methacrylates, oleic acid, linoleic acid, linolenic acid, esters and glycerides of such unsaturated fatty acids, styrene, &agr;-methylstyrene, divinylbenzene, indene and stilbene. Mixtures of the stated olefins may also be used in the proce
Grosch Georg Heinrich
Muller Ulrich
Rieber Norbert
Walch Andreas
BASF - Aktiengesellschaft
Oblon & Spivak, McClelland, Maier & Neustadt P.C.
Siegel Alan
LandOfFree
Single-step method for producing glycol monoethers from olefins does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Single-step method for producing glycol monoethers from olefins, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Single-step method for producing glycol monoethers from olefins will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-2496142