Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing
Reexamination Certificate
2001-02-06
2001-09-25
Padmanabhan, Sreeni (Department: 1621)
Organic compounds -- part of the class 532-570 series
Organic compounds
Oxygen containing
C568S852000, C568S853000
Reexamination Certificate
active
06294705
ABSTRACT:
The invention relates to a method for the preparation of alkali metal alcoholates, in which method alcohol is reacted with alkali metal in an aprotic organic solvent using a hydrogen acceptor.
Alkali metal alcoholates R-OM (R=alkyl, M=Li, Na, K, Rb, Cs) are compounds that are susceptible to hydrolysis and are often used in organic synthesis on account of their basic properties.
It is known that alkali metal alcoholates can be prepared by reacting the corresponding alcohols with an alkali metal in accordance with the reaction equation:
2R—OH+2M→2R—OM+H
2
R=alkyl
M=Li, Na, K, Rb, Cs
The speed of this reaction diminishes as the length of the alkyl chain increases and also as branching increases. Whilst the reaction can be successfully accelerated to a considerable extent on a laboratory scale as a result of the use of extremely finely divided alkali metal, which is produced with a particle size below 50 &mgr;m by means of high-speed stirrers, the reaction takes many hours on an industrial scale of production. Long reaction times, however, impair the economic efficiency of this alcoholate synthesis.
A method for preparing alkali metal alcoholates is known from FR-PS 1 070 601, in which alkali metal is finely distributed, in a boiling inert hydrocarbon by being stirred, and after cooling the calculated quantity of alcohol is added drop by drop to the dispersion. During the preparation of the sodium suspension, any agglomeration of the finely distributed sodium is prevented by adding a dispersive additive, such as fatty acid, surfactants or active carbon. The alkali metal alcoholate in xylene that results can be separated.
With the method known from DE-OS 34 37 152 for the catalyzed preparation of alkali metal alcoholates from alkali amalgams and alcohols, lumps of anthracite are used as the catalyst, the surface of which is preferably coated with a mixture of nickel and molybdenum oxide. Aliphatic alcohols having 1 to 4 carbon atoms are preferably used.
With the method known from DE-PS 08 45 341 for the preparation of alkali metal alcoholates that are lean in caustic alkali, amalgamated alkali metal is brought into contact with alcohol several times in the presence of catalysts, such as graphite. In this connection, it is further known from DE-PS 09 28 467 that finely distributed sodium amalgam and alcohol can be directed in counterflow with respect to a lumpy catalyst, consisting of a mixture of graphite or active carbon and metal filings.
The methods set out above have the following disadvantages:
The reaction times cannot be successfully reduced in an economical manner on an industrial scale of production by means of the use of lumpy or filing-like catalyst substances.
The necessary separation of the catalysts from the reaction product is problematic in many cases.
The use of a toxic amalgam compound as the alkali metal component is problematic on account of the impact on the workplace and environment.
Since the speed of reaction is often simply insufficient unsatisfactory when elemental alkali metal is used, in particular in the case of sterically hindered tertiary alcohols, despite the measures described, very basic organometal compounds have also been used as the alkali- metal source. This holds good in particular for the preparation of lithium alcoholates:
R—OH+R′Li→R—OLi+R′H↑
The disadvantage of this smoothly running reaction is the comparatively high price of organo-lithium compounds.
Further syntheses are based on alkali metal hydrides and amides. Whilst these reagents often react somewhat faster or clearly faster than the alkali metal in elemental form, the compounds, calculated on a molar basis, are clearly more expensive than the alkali metal. In the case of the amides, moreover, ammonia develops that has to be removed from the waste-gas stream at a cost. When hydrides are used—compared with the use of the elemental metals—twice the quantity of hydrogen develops. Whilst hydrogen is not an ecologically hazardous product, the resultant gas stream is loaded with organic compounds (solvent, alcohol) which, for ecological reasons, as far as possible should not reach the environment.
R—OH+MH→R—OM+H
2
↑
R—OH+MNH
2
→R—OM+NH
3
↑
R=alkyl residue; M=alkali metal
The object of the present invention is to avoid the disadvantages in accordance with the prior art, that is, in particular to set forth a method for the preparation of alkali metal alcoholates that starts with inexpensive raw materials that are available commercially and which in a very rapid reaction supplies water-free alkali metal alcoholates whilst forming as few gaseous by-products as possible and without using solid catalysts that are difficult to separate.
The object is achieved in that the alcohol is reacted with the alkali metal (Li, Na, K, Rb, Cs) in an aprotic organic solvent, and an H-acceptor in the form of a conjugated diene or a 1-arylolefine is moreover added thereto. The reaction preferably proceeds in accordance with the following reaction scheme:
The presence of an H-acceptor brings about an advantageous reduction in the quantity of waste gas, from the point of view of reaction-control and environmental-protection, in comparison with the conventional reaction of alkali metal alcoholate formation.
Open-chain or cyclic, unsubstituted or substituted 1,3-dienes or unsubstituted or substituted 1-arylolefines can be used as the H-acceptors (in the case of the substituted reagents, both in the cis and in the trans form). Preferred H-acceptors for this reaction are isoprene, butadiene, cyclohexadiene-(1,3), styrene or methyl styrene.
The quantity of H-acceptor added amounts to 0.2 to 4 times, preferably 0.4 to 1.5 times, the stoichiometric quantity, that is, 0.2 to 4 mol, preferably 0.4 to 1.5 mol, relative to, in each case, 2 mol alcohol. The method can consequently even be carried out with the quantity of H-acceptor that is added lying below the stoichiometrical relationship, this increasing the economic efficiency.
In particular one of the metals Li, Na or K or mixtures of these metals can be used as the alkali metal.
It is advantageous that the alkali metal can be present in pulverulent form, granular form or lumps. In the case of Na, K, Rb or Cs in addition preferably a finely divided molten mass can be chosen. On account of its high melting point, lithium is preferably used in a solid form.
In particular in the case of the reaction of secondary or tertiary alcohols with an alkali metal, the presence of an H-acceptor results in clearly higher speeds of reaction in comparison with methods known hitherto. The reactions of i-propanol, t-butanol or t-pentanol are of particular commercial interest.
An aliphatic or aromatic hydrocarbon with 4 to 20 C-atoms or an ether or a mixture of these substances can be used as the aprotic organic solvent. The reaction can be carried out particularly well in hexane, heptane, octane, toluene, ethyl benzene, methyl-tert. butyl ether (MTBE), tetrahydrofuran (THF) or 2-methyl-THF. Commercially available hydrocarbon mixtures, such as, for example, petroleum ether, paraffin oil, high-boiling Shellsol D 70, can also be used in a particularly advantageous manner as the solvent.
The mixture of alcohol and H-acceptor is preferably added to the dispersion of alkali metal in the aprotic organic solvent. It is also possible to produce a mixture of solvent, H-acceptor and metal, to which the alcohol is added in doses. In some cases, it is also possible to add the alkali metal in a solid or liquid form to the mixture of solvent, alcohol and H-acceptor.
A solution of lithium tert-butylate in THF can be prepared in this way, for example.
The temperature of reaction is maintained at −20 to 200° C., preferably at 20 to 140° C.
REFERENCES:
patent: 4042636 (1977-08-01), Lenz et al.
patent: 4150244 (1979-04-01), Knorre et al.
Emmel Ute
Lischka Uwe
Wietelmann Ulrich
Antonelli Terry Stout & Kraus LLP
Chemetall GmbH
Padmanabhan Sreeni
Price Elvis O.
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