Method for producing guerbet alcohols

Abstract

The invention relates to a method for producing Guerbet alcohols of formula (I), CH3(CH2)nCHR1CH2OH, wherein R1 represents a linear alkyl radical having n−1 carbon atoms, and n represents 3 to 9 carbon atoms. Fatty alcohols of formula (II), R2OH, wherein R2 represents linear alkyl radicals having 6 to 12 carbon atoms, are condensed in the presence of carbonyl compounds and alkali hydroxides.

Description

FIELD OF THE INVENTION

[0001] The invention relates to the field of cosmetic oil bodies or components and concerns an improved method for producing Guerbet alcohols without the use of heavy metal catalysts.

STATE OF THE ART

[0002] Guerbet alcohols represent primary alcohols which are branched in the 2-position and which are obtained by the condensation of linear fatty alcohols. The products are used predominantly as oil components for the production of cosmetic emulsions. The basic starting point for the production thereof is generally fatty alcohols which in a first step undergo self-condensation under the influence of strong bases and heavy metal compounds such as for example copper or zinc oxide. It is assumed that, under the reaction conditions, the alcohol is firstly dehydrated to form the aldehyde, the latter reacting with itself in an aldol condensation and the condensation product is then hydrated to form the alcohol. An overview in that respect is to be found for example in Angew. Chem. 64, 212 (1952).

[0003] There is, however, the disadvantage that the heavy metal catalysts have to be separated off again after the reaction is terminated in order to satisfy statutory requirements and to ensure that they do not cause irritations in the later use. Separation is generally effected by washing with subsequent distillation, in which respect the latter involves not inconsiderable product losses.

[0004] Accordingly the object of the present invention is to provide a method of producing Guerbet alcohols which, compared to the state of the art, operates more economically and with reduced environmental pollution. In particular, the invention seeks to avoid the use of heavy metal catalysts and simple distillative purification of the products should be guaranteed without expensive centrifugal washing.

DESCRIPTION OF THE INVENTION

[0005] The subject-matter of the invention is a method of producing Guerbet alcohols of the formula (I)

CH3(CH2)nCHR1CH2OH   (I)

[0006] wherein R1 represents a linear alkyl radical having n−1 carbon atoms and n represents numbers of between 3 and 9 carbon atoms, wherein fatty alcohols of the formula (II)

R2OH   (II)

[0007] wherein R2 represents linear alkyl radicals having between 6 and 12 carbon atoms are condensed in the presence of carbonyl compounds and alkali metal hydroxides.

[0008] It was surprisingly found that carbonyl compounds, especially fatty aldehydes, as alternatives to heavy metal compounds, also represent suitable catalysts for the Guerbet reaction, in particular if they are added at high temperatures. Accordingly a particular advantage of the method is that the condensation reaction is effected, with comparable levels of yield, in the absence of heavy metals, no washing is required in the finishing operation and thus there are also no longer any product losses.

[0009] Fatty Alcohols

[0010] Fatty alcohols, preferably those of the formula (I) in which R2 represents an alkyl radical having between 8 and 10 carbon atoms are suitable for the condensation operation. Typical examples are hexanol, octanol, decanol, dodecanol and mixtures thereof.

[0011] Carbonyl Compounds

[0012] The carbonyl compounds which are used as catalysts are ketones, and in particular fatty aldehydes which are preferably in accordance with the formula (III)

R3CHO   (III)

[0013] wherein R3 represents linear alkyl radicals having between 6 and 12 and in particular between 8 and 12 carbon atoms. Typical examples are hexanal, octanal, decanal, dodecanal and mixtures thereof. It has proven to be particularly advantageous to use fatty alcohols and fatty aldehydes with the same alkyl radical. Usually the carbonyl compounds in general and the fatty aldehydes in particular are used in amounts of between 0.2 and 50, preferably between 1 and 25 and in particular between 3 and 10 mol %, with respect to the fatty alcohols.

[0014] Condensation

[0015] The condensation reaction can be performed in per se known manner, that is to say the fatty alcohols, together with the bases, are heated to temperatures in the range of between 200 and 250, preferably between 210 and 240° C. The carbonyl compounds can then be added at a temperature of between 20 and 250° C. to the mixture of fatty alcohols and alkali metal hydroxide. It has proven to be advantageous, however, for the addition operation to be implemented at higher temperatures, that is to say between 210 and 240° C. The speed of addition also has an influence on the condensation reaction. Typical times are times of between 0.1 and 10 hours, having regard to the reaction speed and the yields, however, the recommendation is between 10 and 60 minutes. The amount of alkali metal hydroxides can be between 1 and 10, preferably between 3 and 5 mol % with respect to the fatty alcohols. Preferably at least 40% by weight of sodium hydroxide or in particular potassium hydroxide lye is used. At any event, to displace the reaction equilibrium onto the product side it is recommended that the condensation water be continuously distilled off. As organic material is easily entrained in that case it has proven worthwhile to use a dephlegmator, by means of which the organic phase is separated off and can be recycled into the starting material. The work-up procedure which now manages without a washing step then involves simple distillation. This affords fewer product losses and a lower level of waste water pollution.

EXAMPLES

[0016] Example 1. 1000 g (6.3 moles) of decanol (95% by weight) was put in a stirring apparatus comprising a flask, a heating-mantle member, a dephlegmator, a Liebig condenser, a nitrogen transfer device and a double-stroke piston pump, mixed at 20° C. with 22.5 g (0.22 mol) of 45% by weight potassium hydroxide solution and heated to 215° C. The water which occurred upon heating was continuously distilled off. Then 29.6 (corresponding to 3 mol % with respect to decanol) was meteredly added by way of the pump within 60 minutes and in that operation the temperature raised to 240° C. The distilled organic phase was fed to the reaction mixture after phase separation. The reaction was terminated after 6 hours. A GC analysis of the product mixture showed that 76% by weight of 2-octyidodecanol was produced; in addition the reaction mixture contained 6% by weight of trimers, 14% by weight of unreacted monomer alcohol and 4% by weight of mixed Guerbet alcohols consisting of C18- and C22-Guerbet alcohols. Purification of the product was effected distillatively, the unreacted decanol was removed as a first running and was reintroduced into the reaction mixture; the residue that remained was the higher-molecular constituents.

[0017] Example 2. Similarly to Example 1 1000 g (6.3 mol) of decanol was mixed with 22.5 (0.22 mol) of potassium hydroxide solution and 29.6 g of decanal and heated to 240° C. The water produced in the heating operation was continuously distilled off and the distilled organic phase fed to the reaction mixture after phase separation. The reaction was terminated after 6 hours. A GC analysis of the product mixture showed that 43% by weight of 2-octyidodecanol was produced; in addition the reaction mixture contained 2% by weight of trimers, 53% by weight of unreacted monomer alcohol and 2% by weight of mixed Guerbet alcohols consisting of C18- and C22-Guerbet alcohols.

Claims

1. A method for producing Guerbet alcohols of the formula (I)

2. A method as set forth in claim 1 characterized in that fatty alcohols of the formula (I) in which R2 represents an alkyl radical having between 8 and 10 carbon atoms are used.

3. A method as set forth in claim 1 and/or claim 2 characterized in that fatty aldehydes are used as the carbonyl compounds.

4. A method as set forth in at least one of claims 1 to 3 characterized by using fatty aldehydes of the formula (III)

5. A method as set forth in at least one of claims 1 to 4 characterized in that the carbonyl compounds are used in amounts of between 0.2 and 50 mol % with respect to the fatty alcohols.

6. A method as set forth in at least one of claims 1 to 5 characterized in that the carbonyl compounds are meteredly added to the mixture of fatty alcohols and alkali metal hydroxide at a temperature of between 20 and 250° C.

7. A method as set forth in at least one of claims 1 to 6 characterized in that the carbonyl compounds are meteredly added within between 0.1 and 10 hours.

8. A method as set forth in at least one of claims 1 to 7 characterized in that the alkali metal hydroxides are used in amounts of between 1 and 10 mol % with respect to the fatty alcohols.

9. A method as set forth in at least one of claims 1 to 8 characterized in that the condensation products are subsequently purified by distillation.

10. A method as set forth in at least one of claims 1 to 9 characterized in that the condensation operation is performed in the absence of heavy metal catalysts.