Organic compounds -- part of the class 532-570 series – Organic compounds – Unsubstituted hydrocarbyl chain between the ring and the -c-...
Reexamination Certificate
2002-12-04
2004-01-27
Kifle, Bruck (Department: 1624)
Organic compounds -- part of the class 532-570 series
Organic compounds
Unsubstituted hydrocarbyl chain between the ring and the -c-...
Reexamination Certificate
active
06683180
ABSTRACT:
The present invention relates to a process for the preparation of caprolactam from a compound of formula (I):
NC—(CH
2
)
5
—CO—R (I)
in which R is amino, hydroxyl or alkoxy,
wherein
a) a compound (I) or a mixture of such compounds, in the presence of ammonia and optionally a liquid diluent (VI), is hydrogenated with hydrogen in the presence of a catalyst (II) to give a mixture (III),
b) the hydrogen and the catalyst (II) are separated from the mixture (III) to give a mixture (IV), and
c) the mixture (IV), optionally in the presence of a liquid diluent (VII), is converted to caprolactam in the presence of a catalyst (V).
Processes for the preparation of caprolactam from compounds of formula (I) are known per se.
Thus DP 915 568 describes the conversion of cyanovaleric acid esters on Raney cobalt at 120° C. and 200 bar to give caprolactam yields of 40-52%.
The conversion of cyanovaleric acid esters on Raney catalysts is also described in J. Polym. Sci. Part B, Polymer Lett. 2 (1964) no. 5, pages 491-3. Caprolactam yields of 31-74% are obtained.
EP-A-23 751 describes the hydrogenation of cyanovaleric acid esters on Ru/Fe fixed bed catalysts to give caprolactam yields of 35%.
According to JP 305330, cyanovaleric acid esters are first hydrogenated on Raney nickel or Raney cobalt and then thermolyzed without a catalyst to give caprolactam yields of 80-90%.
The disadvantage of these processes is that the yields or space-time yields are too low to meet industrial demands.
It is an object of the present invention to provide a process which makes it possible to prepare caprolactam from compounds of formula (I) in a technically simple and economic manner, avoiding said disadvantages.
We have found that this object is achieved by the process defined at the outset.
According to the invention, the compound (I) used has the formula
NC—(CH
2
)
5
—CO—R (I)
in which R amino, hydroxyl or alkoxy.
It is also possible to use mixtures of such compounds, these also being referred to as the compound (I) in terms of the present invention. It is particularly preferred to use a single compound as the compound (I).
Suitable carboxamide groups are advantageously those of the general formula —CO—NR
1
R
2
, in which R
1
and R
2
independently of one another are hydrogen or an organic radical, preferably C
1
-C
4
alkyl. The particularly preferred carboxamide group is the group —CONH
2
.
Suitable carboxylic acid ester groups are advantageously those of the general formula -CO-OR
3
, in which R
3
is an organic radical, preferably C
1
-C
4
alkyl. The particularly preferred carboxylic acid ester group is the group —CO—OCH
3
.
The preparation of compounds of formula (I) is generally known, for example from Reppe, Lieb. Ann. Chem. 596 (1955) 127, BE 850 113, EP-A-576976 or EP-A-1 107 947.
According to the invention, in step a), the compound (I), in the presence of ammonia and optionally a liquid diluent (VI), is hydrogenated with hydrogen in the presence of a catalyst (II) to give a mixture (III).
Advantageously, at least 0.1 kg, preferably 0.1 to 10 kg, particularly preferably 0.2 to 5 kg and very particularly preferably 0.5 to 5 kg of ammonia should generally be used per kg of compound (I).
Step a) can advantageously be carried out in the presence of a liquid diluent (VI). Suitable diluents (VI) are preferably water or organic diluents, for example C
4
to C
9
alkanols such as n-butanol, i-butanol or n-pentanol, ethers such as methyl tert-butyl ether or tetrahydrofuran, preferably aliphatic hydrocarbons such as n-hexane, cycloaliphatic hydrocarbons such as cyclopentane or cyclohexane, and especially aromatic hydrocarbons such as benzene, toluene, o-xylene, m-xylene, p-xylene, ethylbenzene, i-propylbenzene or di-i-propylbenzene, as well as mixtures of such compounds, for example petroleum ethers. The hydrocarbons can carry functional groups such as halogens, for example chlorine, as in chlorobenzene.
A suitable catalyst (II) is advantageously a heterogeneous catalyst, said catalyst (II) preferably being used as a fixed bed catalyst. A metal selected from the group consisting of Fe, Ni, Co and Ru, or mixtures thereof, is useful as the catalytically active component of the catalyst (II).
Such components can be used as an unsupported catalyst, for example as Raney nickel, Raney cobalt or iron obtained by reduction from synthetic or natural materials containing iron oxide, for example magnetite.
Such components can be used as a supported catalyst. Suitable supported catalysts can advantageously be obtained by impregnating or spraying a support with a solution containing compounds of such metals or mixtures thereof, or by spray drying a suspension containing a support and compounds of such metals or mixtures thereof. Such supported catalysts can contain supports known per se, preferably aluminum oxide, silicon oxide, aluminosilicates, lanthanum oxide, titanium dioxide, zirconium dioxide, magnesium oxide, zinc oxide, zeolites or activated carbon, or mixtures thereof.
In step a), the proportion of compound (I), based on the sum of the starting components, namely compound (I), ammonia and diluent (VI), is advantageously 0.1 to 50% by weight, preferably 1 to 30% by weight and particularly preferably 2 to 20% by weight.
The reaction can advantageously be carried out in the liquid phase.
The reaction can advantageously be carried out at temperatures generally of 40 to 250° C., preferably of 50 to 100° C. and particularly preferably of 60 to 120° C. The pressure should generally range from 1 to 350 bar, preferably from 25 to 250 bar.
The reaction of step a) yields a mixture (III).
In step b), the hydrogen and the catalyst (II) are separated from the mixture (III) to give a mixture (IV).
The catalyst (II) can be separated off in a manner known per se.
In the case of a suspension procedure, the catalyst (II) can advantageously be separated off by filtration, especially through a membrane of appropriate pore size. In the case of a fixed bed procedure, the reaction mixture can advantageously be withdrawn from the reactor to leave the catalyst (II) in the reactor.
The hydrogen can be separated off in a manner known per se, preferably in a high pressure separator. The high pressure separator can advantageously be followed by [text missing] for separating off any remaining hydrogen.
All or part of the ammonia can advantageously be separated off in step b).
The separation can advantageously be carried out by distillation, especially at bottom temperatures of 60 to 220° C. and pressures of 1 to 30 bar.
A mixture (IV) is obtained after step b).
According to the invention, in step c), a mixture (IV), optionally in the presence of a liquid diluent (VII), is converted to caprolactam in the presence of a catalyst (V).
Step c) can advantageously be carried out in the presence of a liquid diluent (VII). Suitable diluents (VII) are preferably water or organic diluents, for example C
1
to C
9
alkanols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, i-butanol or n-pentanol, preferably aliphatic hydrocarbons such as n-hexane, cycloaliphatic hydrocarbons such as cyclopentane or cyclohexane, and especially aromatic hydrocarbons such as benzene, toluene, o-xylene, m-xylene, p-xylene, ethylbenzene, i-propylbenzene or di-i-propylbenzene, as well as mixtures of such compounds, for example petroleum ethers. The hydrocarbons can carry functional groups such as halogens, for example chlorine, as in chlorobenzene.
Advantageously, the diluents (VI) and the diluents (VII) can be identical.
A suitable catalyst (V) is advantageously a heterogeneous catalyst. The catalyst (V) can preferably be used as a fixed bed catalyst.
Suitable catalysts (V) are acidic, basic or amphoteric oxides of the elements of main group II, III or IV of the periodic table, such as calcium oxide, magnesium oxide, boron oxide, aluminum oxide, tin oxide or silicon dioxide in the form of pyrogenic silicon dioxide, silica gel, kieselguhr, quartz or mixtures thereof, and also oxides of metals of subgroups II to VI of the periodic tab
Ansmann Andreas
Fischer Rolf-Hartmuth
Melder Johann-Peter
Ohlbach Frank
BASF - Aktiengesellschaft
Keil & Weinkauf
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