DE2150992C3 - Process for the production of α, ß-unsaturated ketones - Google Patents

Description

IO

in which R ¹ and R ^{2 represent} a branched or unbranched, saturated or unsaturated aliphatic or cycloaliphatic-aliphatic hydrocarbon radical having 1 to 20, preferably 1 to 16 carbon atoms or a saturated or unsaturated cycloaliphatic hydrocarbon radical having 5 to 12 carbon atoms, the may also contain alkyl groups as substituents and / or an endoalkylene group or represent an araliphatic hydrocarbon radical with 7 to 15 carbon atoms or an aromatic hydrocarbon radical, preferably a phenyl group, R ³ denotes hydrogen or an aliphatic hydrocarbon radical with 1 to 10 carbon atoms , and in addition R ¹ and R ³ together with the two adjacent carbon atoms can denote members of a common alicyclic ring, by reaction of an aldehyde of the general formula I!

R ²

C = O H

(H)

in which R ^{2 has} the aforementioned meaning with a ketone of the general formula III

HO
H — C — C — R ¹

(III)

R ³

in which R ¹ and R ^{3 have} the abovementioned meaning, in the liquid phase, characterized in that the reaction is carried out in the presence of a catalyst which consists of at least 80% zinc oxide.

45

50

Furthermore it is au, u *. ~~ · - ~ - ~ ²⁵⁴⁹⁵⁰ p

known. Aldehydes and ketones be. Temperatures of 500-1000 C in the presence of hydrogen and in the presence of a catalyst consisting essentially of Z.nkox.d and 1 to 15% by weight of zirconium oxide in the gas phase to form unsaturated ketones with a higher molecular weight. Be. However, this process only achieves low conversions and low yields. In addition, reactions require _m the presence of hydrogen at the temperatures mentioned for security reasons a high technical effort. Furthermore, with such reactions in the gas phase, cracking processes occur on the contact surface, which negatively influence the service life of the contact.

Furthermore, from the German patent specification 12 03 243, the implementation of two identical or various aldehydes or ketones in the nutty phase at elevated temperature and in the presence of a by firing a mixture of Molybdanox.d, magnesium oxide and optionally zinc oxide or Compounds of these metals obtained from the catalyst to give "^ -unsaturated aldehydes or ketones are known. According to the process of this patent, in the condensation of aldehydes with one another, especially in the condensation of n-butyraldehyde to 2-EthyIhexenal, good conversions and very good Yields of ", ^ - unsaturated aldehydes obtained.

For the implementation of aldehydes with ketones too The process of German patent specification 12 03 243 is less suitable for-unsaturated ketones; significantly lower conversions and selectivities are achieved. This is particularly clear if you don't just use isobutyraldehyde, i.e. an aldehyde that cannot condense with itself, according to the method of German Patent 12 03 243 reacts with a ketone, but aldehydes used that easily condense on themselves, such as 3,3-dimethylacrolein and citral (s. Comparative experiment: Example 23).

A process has now been found for the production of - unsaturated ketones of the general formula 1

HR ³

It is from H ο ube η - W ey 1, Methods der • ganischen Chemie, Volume 7/1, pages 77 ff, and Organic eactions, Volume 16, pages 27-47, 69-78, 177 ff.,; Know, that you can convert aldehydes and ketones to a, /? - unsaturated ketones. Temperatures of 5 to 5 ⁰ C for this aldolization preferably (Organic eactions, loc.cit., Page 77). The numerous catalysts used in these processes, for example alkali and alkaline earth metal hydroxides, organic bases, alkali salts, and alcoholates, at the same time also favor the self-conensation of the aldehydes or ketones and, in some cases, allow larger amounts of byproducts to arise Such mixtures; t associated with greater effort, since the use of R ¹ and R ² for a branched or unbranched, saturated or unsaturated aliphatic

see or cycloaliphatic-aliphatic hydrocarbon radical with 1 to 20, preferably 1 to ^ carbon atoms or a saturated or unsaturated cycloaliphatic Hydrocarbon radical with 5 to ^ C atoms, which also has alkyl groups as substituents and / or

may contain an endoalkylene group or for an araliphatic hydrocarbon radical having 7 to 15 carbon atoms, preferably a benzyl group, or an aromatic hydrocarbon radical, preferably seven pheny groups, R ^{3 is} hydrogen or one.

aliphatic hydrocarbon radical with 1 to 10 carbon atoms and, in addition, R ¹ and R ³ together with the two adjacent carbon atoms are members of a common alicyclic

can denote tinges by reacting ■ an aldehyde of the general formula II

R ² -C = O
H

(Π)

in which R ^{2 has} the aforementioned meaning with a ketone of the general formula HI

HO

I 11

HCCR ¹

(HD in each case 1 carbon atom less than the corresponding radicals R ^. Preferred aldehydes of the formula Ha come into consideration, in which the radical R ^{2a represents} a branched or unbranched, saturated or unsaturated aldehyde

see hydrocarbon residues with 1 to 15 carbon atoms a cycloaliphatic hydrocarbon radical with 5 up to 9 carbon atoms, including alkyl groups as substituents can carry, or an araliphatic group with / up to 10 carbon atoms.

> As aldehydes that easily condense on themselves aldehydes of the general formula Mb are also suitable.

in which R ¹ and R ^{3 have} the aforementioned meaning, found, which is carried out in the liquid phase, the reaction taking place in the presence of a catalyst, which consists essentially of zinc oxide.

This process enables the production of these unsaturated ketones by reacting aldehydes, especially aldehydes with a tendency to self-condensation, with ketones with good conversions and very good ones Exploit.

This result is particularly surprising, since German patent 12 03 243 based on Catalyst comparisons using the example of the condensation of n-bulyraldehyde to 2-Ethyi-hexenal to the The result was that zinc oxide alone or in combination with just one of the other oxide components results in poorer conversions and selectivities in the process of this patent than that from the 3-component catalyst. It was also surprising that the catalytic conversion in liquid phase is also beneficial for unsaturated and sensitive aldehydes and ketones.

Suitable aldehydes are those aldehydes of the formula II in which R ^{2 represents} a branched or unbranched, saturated or unsaturated aliphatic or cycloaliphatic-aliphatic hydrocarbon radical having 1 to 20, preferably 1 to 16 carbon atoms or a saturated or unsaturated cycloalinatic hydrocarbon radical having 5 to 12 carbon atoms which can also contain alkyl groups as substituents and / or an endoalkylene group, or which represents an araliphatic hydrocarbon radical with 7 to 15 carbon atoms, in particular a benzyl group, or an aromatic hydrocarbon radical, preferably a phenyl group.

The process according to the invention is particularly advantageous for the reaction of an aldehyde, the easily condensed with itself, with a ketone, since both the process of German patent specification 12 03 243 as well as the known Condensation reactions in the presence of alkaline condensing agents are not very beneficial.

As aldehydes that easily condense with themselves, for example, aldehydes of the general type Formula Ha into consideration.

R ^2c

_R 2fc-C = CH-C = O H

(Hb)

R ² "-CH ₂ -C = H

(II a)

The radical R ^2s in this formula generally has the ^{meaning given above for R 2} , but contains The radical R ²ⁱ⁾ in this formula generally has the ^{meaning given above for R 2} , but contains 2 to 4 fewer carbon atoms in each case the corresponding radicals R ² . The radical R ^2c in the formula lib generally stands for a methyl group or an ethyl group. Preference is given to aldehydes of the formula Hb in which R ^{2b is} a branched or unbranched, saturated or unsaturated aliphatic hydrocarbon radical having 1 to 12 carbon atoms. The reaction of aldehydes of the formula Hb with ketones is of particular technical interest, since in this reaction Ä, ß, y, o-unsaturated ketones are formed which, for example, Some of them play an important role in terpene chemistry - and so far could only be produced in a cumbersome way. The reactions of such alkali and temperature-sensitive aldehydes as 3,3-dimethylacrolein, citral and farnesal with acetone to 2-methyl-2,4-heptadien-6-one, pseudojonone and farnesal acetone should be emphasized.

For example, the aldehydes mentioned below are suitable for the reaction according to the invention:

Acetaldehyde, propionaldehyde, n-, iso-, tert-butyraldehyde, crotonaldehyde, tiglinaldehyde, 3,3-dimethylacrolein, önanthaldehyde, citral, <x ~ and / J-cyclocitral, benzaldehyde, cinnamaldehyde, phenylacetaldehyde, hydrozinwaldehyd, 2-phenyl- propionaldehyde, cyclohexylaldehyde, n-valeraldehyde, i-valeraldehyde, anisaldehyde and n-heptaldehyde, farnesal, phytal, vitamin A aldehyde. Suitable ketones are those ketones of the formula III in which R ^{1 represents} a branched or unbranched, saturated or unsaturated aliphatic or cycloaliphatic-aliphatic hydrocarbon radical having 1 to 20, preferably 1 to 16, carbon atoms or a saturated or unsaturated cycloaliphatic Hydrocarbon radical with 5 to 12 carbon atoms, which also has alkyl groups as substituents and / or an endoalkylene. appe or an araliphatic hydrocarbon radical with 7 to 15 carbon atoms, preferably a benzyl group, or an aromatic hydrocarbon radical, preferably a phenyl group, R ^{3 is} hydrogen or an aliphatic hydrocarbon radical with 1 to 10 carbon atoms: n, preferably Is hydrogen, and in addition R ¹ and R ³ together with the two adjacent carbon atoms can denote members of a common alicyclic ring.

When using a ketone that has both a methylene and a

Possesses a methyl group, for example methyl ethyl ketone, takes place in contrast to the known condensation processes the reaction predominantly takes place on the methyl group.

The best yields are obtained when using cycloalkanones or those ketones which carry a methyl group in the position to the carbonyl group, that is to say ketones in which R ^{3 is} hydrogen or R ¹ and R ³ with the two adjacent carbon atoms are members of a common acyclic ring describe.

From a technical point of view, the implementation with unsaturated ketones is again of particular interest here whose condensation products with aldehydes play an important role in the fragrance industry. »5

In particular, «, ^ - unsaturated ketones should be emphasized, d. i.e., ketones of the formula purple

HO R ¹⁶

HCC-CH = CR ¹ '
R ³

(HIa)

in which R ^{3 has} the meaning given above, R ^la for a branched or unbranched saturated or unsaturated aliphatic or cycloaliphatic-aliphatic hydrocarbon radical with 1 to ί8, preferably 1 to 14 carbon atoms or a saturated or unsaturated cycloaliphatic hydrocarbon radical with 5 to 10 C. -Atoms, which can also contain alkyl groups as substituents, and R ^{14> stands} for hydrogen or an alkyl group with 1-4 C atoms. This means that - - unsaturated ketones prepared according to the invention can be reacted again if the process is carried out appropriately.

Examples of suitable ketones of the formula III are: acetone, methyl ethyl ketone, methyl n-propyl ketone, Methyl isopropyl ketone, methyl n-butyl ketone, Methyl isobutyl ketone, methyl t-butyl ketone, diethyl ketone, Diacetyl, 2-methyl-2-hepten-6-one, acetophenone, cyclohexanone, cyclohexyl ethyl ketone, benzyl methyl ketone, Methyl propenyl ketone, ethyl propenyl ketone, mesityl oxide, Propyl propenyl ketone, isobutylidene acetone, 2-methyl-2,4-heptadien-6-one, jJ-ionone, farnesylacetone and geranylacetone.

According to the invention, a catalyst consisting essentially of zinc oxide is understood to be a catalyst which consists of at least 80%, preferably practically completely, zinc oxide. It may contain small amounts, ie 0 to 20%, of metal oxides or inert fillers which, under the reaction conditions, do not cause any other conversions of the starting materials. However, if possible, it should not contain any significant amounts of metal oxides which accelerate the self-condensation of aldehydes, such as Al2O3, Fe ₂ O ₃ , PtO ₂ , MOO3, Fe ₂ O3 or MgO.

Furthermore, the catalyst should not contain any significant amounts of acidic components such as Cr ₂ Oa, Sb ₂ O3 and Bi ₂ O3, since otherwise cyclization reactions often occur when unsaturated starting materials are converted.

It is particularly advantageous to work with practically pure zinc oxide in the form of tablets or strands with a diameter of about 4 to 5 mm, as used in the art, for example, in the dehydrogenation of cyclohexanol to be used as a catalyst to cyclohexanone.

Of course, the zinc oxide contact can also be inert under the reaction conditions Apply carrier materials such as pumice stone, dead-burned clay or charcoal.

To carry out the process, a mixture of the starting materials and the catalyst is kept, optionally together with a solvent, for the duration of the reaction at the reaction temperature and optionally the reaction pressure. The end product is then derived from the reaction mixture the usual way, e.g. separated by fractional distillation. The reaction can be discontinuous or be carried out continuously. In the case of the discontinuous process, it is expedient to work in one Shaking autoclave. In the continuous process, one works in a reactor or a reactor Stirred tank cascade by z. B. the liquid starting mixture pressureless at the reaction temperature or under pressure through a catalyst layer

directs. . .

The starting materials can be reacted with one another in stoichiometric amounts. In many cases it is abpr beneficial, the cheaper and more stable component the ketone, in an excess of about 0.5 to 6 moles, preferably 1 to 4 moles, per mole of aldehyde use.

If you work with stable ketones such as acetone, methyl ethyl ketone and mesityl oxide, then you work advantageously with 3 to often the stoichiometric Amount, so practically uses an excess of ketone as a solvent. Less with condensation In contrast, stable ketones are advantageously only used in stoichiometric to twice stoichiometric amounts of ketone and an inert solvent.

The catalyst concentration can be varied within wide limits. So can with discontinuous Operation already with amounts of 1 to 60, preferably 5 to 50 wt .-%, based on the amount of aldehyde, high conversions and yields can be achieved. In the case of continuous operation, however, the catalyst concentration can are considerably higher. Here, in general, amounts of aldehyde from 1 to 100, preferably from 5 to 60% by weight, based on the amount of catalyst, worked. With continuous The process is generally carried out per hour from 0.1 to 10 liters of the reaction mixture per liter Catalyst passed over the catalyst. The catalyst can usually last up to a year without it Regeneration can be used.

The reaction is generally conducted at a temperature of 30 to 240 ⁰ C, preferably at a temperature of 135-205 ⁰ C is performed. Temperatures above 205 ° C. are generally only necessary if one starts out from ketones which have no methyl group in relation to the carboxyl group. The process is carried out without pressure or under pressure, preferably at pressures between 20 and 100 atm. The pressure and temperature are chosen so that the reaction mixture is liquid in each case.

The reaction time for such reactions depends on the reaction temperature and reactivity Starting compounds between 5 minutes and 20 hours, preferably 1/2 hour to 10 hours.

The reaction can be carried out without solvent, but also in the presence of under the reaction conditions carry out inert solvents. Dialkyl ethers such as di-n-butyl ether and aliphatic can be used as solvents

Hydrocarbons, such as ligroin, or aromatic hydrocarbons, such as toluene or xylene, are suitable. The solvents are used in about 2 to 5 times the amount by weight, based on the sum of the Weight of the starting components.

Since the resulting compounds are sensitive to air, it has proven advantageous to carry out the reaction in the absence of air, for example under a nitrogen or argon atmosphere.

With the help of the method according to the invention, it is possible to carry out a series of single or multiple unsaturated higher molecular weight ketones in a simple manner and with good conversions and excellent Produce yields. The catalyst used with preference is a catalyst customary in the art, which can be used for a long time without regeneration.

Side reactions, e.g. B. Aldolization of the aldehyde, polymerizations, the formation of numerous by-products or additional isomers due to isomerization of the double bond, do not occur in any significant amount Dimensions on. The end product can generally be obtained from the reaction mixture in a simple manner, e.g. B. by Distillation, can be separated off without the catalyst having to be separated off beforehand. Special measures, in order to quickly remove the end product which is formed from the reaction mixture, even with the Establishing very sensitive connections is not necessary, which is beneficial to operational safety and security Effectiveness of the process.

The end products which can be prepared by the process of the invention are partly solvents and partly valuable intermediate products for the production of fragrances, solvents, dyes, plastics and various natural substances. For example, the pseudo-ionone which can be produced according to the invention is a important intermediate product for the production of vitamin A and vitamin E. Numerous ketones such as Methylheptadienone, farnesal acetone, anisal acetone and benzalacetone are themselves of interest as odoriferous substances found.

By hydrogenation in the presence of palladium on activated carbon or Raney nickel as a catalyst you can the corresponding saturated ketones are produced from the unsaturated. Regarding their use reference is made to the publications mentioned and to Ulimann's Encyclopedia of Technical Chemistry, Volume 9, pages 544 ff., Referenced.

The examples given below are intended to explain the process of the invention in more detail. The ones in the Unless otherwise stated, parts mentioned in the examples are parts by weight. Parts of the room relate to Weight units such as liters to kilograms. The catalysts were used in the old examples in the form of 4 mm strands.

example 1

A mixture of 50 parts of 3,3-dimethylacrolein and 100 parts of acetone with 12 parts of zinc oxide is ^{heated for 3 hours at 180 °} C. and 45 atm. Pressure in a shaking autoclave. The reaction vessel is then cooled and the mixture is fractionally distilled. 52.5 parts of 2-methyl-2,4-hepladicn-6-one are obtained in a yield of 93% of theory, based on 3,3-dimethylacrolein, with a conversion of 76% of theory and a boiling point of 92 "C at 15 torr.

Comparative experiment

50 parts of 3,3-dimethylacrolein and 100 parts of acetone are mixed with 12 parts of a contact which was produced according to patent 12 03 243 by burning a mixture of equimolar amounts of magnesium oxide, molybdenum oxide and zinc oxide for 3 hours at 180 ^° C. and 30 at Pressure heated. In the subsequent fractional distillation, 27 parts of 2-methyl-2,4-heptadien-6-one are obtained, which corresponds to a yield of 43% of theory with a conversion of 86% (based on 3,3-dimethylacrolein).

Example 2

Analogously to Example 1, a mixture of 50 parts of 3,3-dimethylacrolein and 100 parts of cyclohexanone is used 12 parts of zinc oxide for 4 hours at 180 ° C and 50 atm pressure heated. After cooling and distilling the mixture, it has a boiling range of 93 to 96 ° C at 0.1 torr 70.5 parts of 2- (3'-methyl-2-butenylidene) cyclohexanone. The conversion is 81% of theory a yield of 89% of theory (based on 3,3-dimethyl-acrolein).

₂ , B eis ρ ie 1 3

50 parts of 3,3-dimethylacrolein and 100 parts of acetophenone are kept under a pressure of 50 atm together with 10 parts of zinc oxide at a temperature of 180 ^° C. for 3 hours. Fractional distillation of the reaction mixture gives 75.3 parts of 2-methyl-6-phenyl-2,4-hexadien-6-one (87% of theory, based on 3,3-dimethylacrolein) with a conversion of 78% of theory . Kp., ₀ _ 4 = 107 to 110 ⁰ C.

_3S B eis ρ ie 1 4

In a rocking autoclave, 50 parts of 3,3-dimethylacrolein and 100 parts of methyl ethyl ketone I ^1/2 hours 10 parts of zinc oxide at 180 ⁰ C and pressure at 50 to be implemented. Analogously to Example 1 49.4 parts obtained when working up the reaction mixture of 2-methyl-2,4-octadiene-6-one from Kp.t9 = 106 ⁰ C. The conversion is 68% of theory, the yield 88% of theory based on 3,3-dimethylacrolein.

Example 5

Citral 50 parts and 100 parts of acetone are reacted a catalyst ^3/4 hour at 200 ⁰ C and 80 atm pressure in the presence of 12 parts consisting of 12Gew .-% copper (U) oxide and 88Gew .-% Zinkoxic. Analogously to Example 1, 45.6 divided pseudoionone with a boiling point of 9O ⁰ C be 0.01 Torr. The conversion is 82% of theory, ie the yield, based on citral, is 88% of theory.

_{ss exampleö}

In an autoclave, 50 parts and 100 parts of acetone are Crotonaldehyi 'heated / 2 hour at 14O ⁰ C and 30 a pressure with 15 parts of zinc oxide. Analogously to the example, 38.4 parts of 2,4-heptadien-6-ones with a boiling point of bp.63 "C. are obtained in a yield of 75% of theory, based on crotonaldehyde, with a conversion of 65% of theory.

Example 7

<> 5 60 parts and 90 parts acetone Isovalcrtildchyd'll heated for 2 hours at 18O ⁰ C and 35 printing with 15 parts of zinc oxide. Analogously to Example I, 56.4 parts of 2-methyl-4-hcpten-6-one with a boiling point of 750 = 176 ° C. are obtained (corresponding to

709 642 /

accordingly a yield of 81% of theory, based on isovaleraldehyde, and a conversion of 73% of the Theory).

Example 8

A mixture of 20 parts of acetaldehyde and 120 parts of acetone is ^{heated with 14 parts of zinc oxide for 3 hours at 140 °} C. and 30 atm. Pressure. The subsequent fractional distillation gives 28.7 parts of 3-penten-2-one with a boiling point of 122 ° C. at normal pressure. The yield is 75% of theory, based on acetaldehyde, with practically complete conversion of the acetaldehyde.

Example 9

60 parts of benzaldehyde, 120 parts of acetone and 18 parts of zinc oxide are ^{heated for 5 hours at 180 °} C. and 50 atm. Pressure. In the subsequent fractional distillation, 60.8 parts of crystalline benzalacetone with a melting point of 42 ° C. and a boiling point of 760 = 262 ° C. are obtained. The yield is 92% of theory (based on benzaldehyde) with a conversion of 80% of theory.

Example 10

A mixture of 50 parts of 3,3-dimethylacrolein and 120 parts of cyclopentanone are mixed with 17 parts of zinc oxide added and heated for 3 hours at 180 ° C and 50 atm pressure. Analogously to Example 9, 63.5 parts of 2- (3'-methyl-2'-butenylidene -) - cyclopentanone are obtained with a boiling point of bp 0.01 = 61-63 ° C in a yield of 90% of theory (based on 3,3-dimethylacrolein) with a conversion of 79% of theory.

Example 11

100 parts of methylnorbornyiketone, 50 parts of 3,3-dimethylacrolein and 15 parts of zinc oxide are heated for 5 hours at 180 ° C. and 55 atmospheres pressure. Analogously to Example 9, 85.7 parts of (4-methyl-1,3-pentadienyl) norbornyl ketone with a boiling point of boiling point = HO ⁰ C are obtained. The yield is 88% of theory with a conversion of 80% ( based on 3,3-dimethylacrolein) of theory.

Example 12

100 parts of methyl ethyl ketone, 50 parts of citral and 8 parts of zinc oxide are ^{heated for 2 hours at 200 °} C. and 60 at pressure. In the franktionierten distillation of the reaction mixture 51.5 parts obtained 7,11-dimethyl-4,6,10-dodecatrien-3-one having a boiling point of 105-108 ⁰ C. Kp.0.01 = The yield is 85% of theory at a conversion of 76% (based on citral) of theory.

Example 13

100 parts of methyl ethyl ketone, 50 parts of isovaleraldehyde and 10 parts of zinc oxide are heated for 5 hours at 16O ⁰ C and 40 atm pressure. Analogously to Example 9, 48 parts of 7-methyl-4-octen-3-one (which still contain 3% by weight of 3,6-dimethyl-3-hepten-2-one) with a boiling point of boiling point = 71- are obtained. 73 ° C. The yield of 7-methyl-4-octen-3-one is 80% of theory with a conversion of 71% (based on isovaleraldehyde) of theory.

Example 14

40 parts of propionaldehyde. 120 parts of acetone UNRL 8 parts of zinc oxide are heated for 5 hours at 140 ⁰ C and 35 atm pressure. Fractional distillation of the reaction mixture gives 47.7 parts of 3-hexen-2-one with a boiling point of bp ₇₆ ° = 140.degree. With an 86 percent conversion, the yield is 82% of theory (based on propionaldehyde).

Example 15

50 parts of anisaldehyde, 100 parts of acetone and 15 parts of zinc oxide are V2 hours at 200 ° C. and 60 atmospheres pressure heated. Analogously to Example 9, 46.2 parts of 4- (p-methoxyphenyl) -3-buten-2-one are obtained in the form of yellowish crystals and with a melting point = 74 ° C and bp 0.1 = 109-110 ° C. The yield is 90% of theory (based on anisaldehyde) with a conversion of 79% the theory.

Example 16

120 parts of 2-methyl-1-hepten-6-one, 40 parts of 3,3-dimethylacrolein and 10 parts of zinc oxide are ^{heated for 5 hours at 180 °} C. and 60 atmospheres pressure. Analogously to Example 9 to obtain 63.5 parts of 2,10-dimethyl-2,4,10-undecatrien-6-one having the boiling point Kp. _0, i = 120 to 123 ⁰ C. The yield is 91% of theory (based to 3,3-dimethylacrolein) at a conversion of 78% of theory.

Example 17

50 parts of 1,1,5-trimethyl-2-formyl-cyclohexa-2,4-diene, 110 parts of acetone and 16 parts of zinc oxide are ^{heated for 1 hour at 200 °} C. and 80 atm. Pressure. Analogously to Example 9, 33.6 parts of 4- (r, r, 5'-trimethylcyclohexa-2 ', 4'-dien-2'-yI) -3-buten-2-one with a boiling point of bp 0.01 = 93 are obtained -94 ° C. The conversion is 63% of theory and the yield (based on 1,1,5-trimethyl-2-formyl-cyclohexa-2,4-diene) is 84% of theory.

Example 18

100 parts of acetone, 60 parts of isobutyraldehyde and 8 parts of zinc oxide are ^{heated for 3 hours at 160 °} C. and 35 atm. Pressure. Analogously to Example 9, 54.5 parts of 5-methyl-3-hexen-2-one (isobutylidene _acetone ) with a boiling point of 76O = 155.degree. C. are obtained. The yield is 83% of theory (based on isobutyraldehyde) with a conversion of 70% of theory.

Example 19
A substance mixture of 50 parts of 3,3-dimethylacrolein and 100 parts of mesityl oxide is heated in a shaking autoclave with a content of 250 parts by volume for 3 hours with 12 parts of zinc oxide at 180 ° C. and 60 atmospheres pressure. In the subsequent fractional distillation of the reacted product, 54.8 parts of 2,8-dimethyl-2,5,7-nonatrien-4-one with a boiling point of 0.4 ° C = 82 ° C. are obtained. The conversion is 72%, the yield (based on 3,3-dimethylacrolein) 78% of the

Theory.

Example 20

In the same reaction vessel as in Example I, a reaction mixture of the same composition as in Example 19 is reacted with 12 parts of zinc oxide for 5 hours at 160 ^° C. and 45 atmospheres pressure. Working up gives 58.5 parts of 2,8-dimethyl, 2,5,7-nonatrien-4-one. The conversion is now 68% and the yield is 88% (based on 3,3-dimethylucrolein).

Example 21

100 parts of 2-methyl-2.4-hcptadicn-6-one and 50 parts of 3,3-dimethylacrolein were ir

heated in an autoclave for 2 hours at 160 ⁰ C and 30 atm pressure. In the distillative working up of the reaction:> product are obtained in the form of yellow crystals 68.8 parts of 2,10-dimethyl-2,4,7,9-undecatetraen-6-one having a boiling point of ₁₀ Kp _4 = 96 °. C. The yield (based on 3,3-dimethylacrolein) is 92% of theory and the conversion is 66%.

Example 22

A mixture of 150 g of β-] onone and 60 g of 3,3-dimethylacrolein is stirred in a 2-liter round bottom flask for 10 hours at 145 ° C. without pressure with 20 g of zinc oxide. The water formed during the condensation is removed immediately by feeding pentane into the vapor space above the reaction mixture. When the reaction product is fractionated, 112 parts of 1- (2 '-, 6', 6'-trimethyl-r-cyclohexen-r-yl) -7-methyl-l, 4,6-octatrien-3-one are obtained with a boiling point of Kp., ₀ _ ₄ = 120-122 ° C. The result is a yield of 93% of theory with a conversion of 65% (based on 3,3-dimethylacrolein).

Example 23

A mixture of 30 parts of i-butyraldehyde and 90 parts of acetone is worked up after 2 hours heating with 12 parts of zinc oxide at 16O ⁰ C and 45 atm pressure. 27.5 parts of 5-methyl-3-hexen-2-one are obtained. The yield is 94% of theory with a conversion of 68% (based on i-butyraldehyde).

Example 24

In a Schütteiautoklav with a content of 2,000 parts by 310 parts of farnesal are reacted with 1200 parts of acetone in the presence of 150 parts Zinc oxide 5 hours at 180 ⁰ C and 30 atm pressure. In the distillative working up, 280 parts Farnesalaceton with the boiling point Kp. ₁₀ _4 = 128-130 ⁰ C. This results in a yield of 93% of theory (based on farnesal), at a conversion of 88%.

Example 25

A mixture of 150 parts of 2-methyl-1-hepten-6-or and 50 parts of citral is mixed with 20 parts of zinc oxide ir

2Ci heated a round bottom flask with stirring for 4 hours at 16O ⁰ C and atmospheric pressure. The resulting water is removed by distillation. The subsequent * fractionation gives 61 parts of 2,10,14-trimethyl-penta deca-l, 7,9,13-tetraen-6-one with a boiling point of bp ₁₀ _

_Z5 = U8-12O ⁰ C. The yield is 88% of the theory (based on citral), with a conversion of 81%.

Claims (1)

Claim ': e catalyst must be removed again or neutralized before work-up. D.e yields Process for the production of «, ^ - unsaturated Ketones of the general formula 1 R ² -C = CCR ¹ HR ³ (I)