Claims
- 1. A process for the preparation of an aromatic amine of the formula ##STR6## in which R.sup.1 and R.sup.2 independently of one another denote hydrogen or straight-chain or branched C.sub.1 -C.sub.5 -alkyl or C.sub.1 -C.sub.5 -alkoxy and together may also denote a fused benzene ring, and
- R.sup.3 and R.sup.4 independently of one another represent straight-chain or branched C.sub.1 -C.sub.10 -alkyl or C.sub.3 -C.sub.10 -cyclo alkyl, and R.sup.4 can additionally represent hydrogen,
- comprising the catalytic reaction of an aromatic amine of the formula ##STR7## with an alkanol of the formula
- R.sup.3 OH
- or the associated ethers R.sup.3 --O--R.sup.3, wherein
- R.sup.3 and R.sup.4 have the above meaning,
- at elevated temperature, wherein the reaction is carried out at 160.degree.-400.degree. C. in the gas phase in the presence of a copper catalyst on an Al.sub.2 O.sub.3 -containing carrier which is impregnated with compounds of manganese and of one or more rare earth metals, having a Cu content of 0.1-5% by weight, a total content of compounds of manganese and of the rare earth metal or metals of 0.05-8% by weight, calculated as metals, the weight ratio of rare earth metal(s) to manganese being 5:1-1:5, calculated as metal, and all percentages being relative to the total weight of the catalyst, and 0.5-20 mol of alkanol per mol of the aromatic amine being employed.
- 2. The process of claim 1, wherein the aromatic amine is of the formula ##STR8## in which R.sup.1 and R.sup.2 independently of one another denote hydrogen, straight-chain or branched C.sub.1 -C.sub.5 -alkyl or C.sub.1 -C.sub.5 -alkoxy.
- 3. The process of claim 2, wherein the aromatic amine is prepared in an alkylation reactor with simultaneous addition of hydrogen from the parent nitro compound of the formula ##STR9##
- 4. The process of claim 1, wherein the gas-phase reaction is carried out under a pressure of 0.5 to 10 bar.
- 5. The process according to claim 1, wherein in the catalyst the Cu content is 0.1-3% by weight, relative to the total weight of the catalyst.
- 6. The process of claim 5, wherein the Cu content is 1-3% by weight, relative to the total weight of the catalyst.
- 7. The process according to claim 1, wherein in the catalyst the total content of compounds of manganese and of the rare earth metal or metals is 0.2%-5% by weight, calculated as metals.
- 8. The process according to claim 1, wherein in the catalyst the weight ratio of rare earth metal(s) to manganese is 10:9-1:2, calculated as metal.
- 9. The process according to claim 1, wherein in the catalyst the carrier is .alpha.-Al.sub.2 O.sub.3 or .gamma.-Al.sub.2 O.sub.3.
- 10. The process according to claim 1, wherein the the catalyst has an additional content of 1-6% by weight, relative to the total weight of the catalyst, of alkali metal hydroxide.
- 11. The process of claim 10, wherein the alkali metal hydroxide is lithium hydroxide, sodium hydroxide, potassium hydroxide or a mixture of these.
- 12. The process of claim 11, wherein the alkali metal hydroxide is sodium hydroxide, potassium hydroxide or a mixture of these.
- 13. The process according to claim 1, wherein the catalyst is prepared by treatment of the carrier with soluble compounds of manganese and of the rare earth metal or metals, conversion of these compounds into compounds which adhere firmly to the carrier, by drying and subsequent heating at 200.degree.-450.degree. C., impregnation of the heated carrier thus obtained with a soluble copper salt and fixing of the copper on the carrier.
- 14. The process of claim 13, wherein the subsequent heating is carried out at 250.degree.-430.degree. C.
- 15. The process of claim 13, wherein after fixing the copper on the carrier a treatment for activation with hydrogen is carried out at 150.degree.-350.degree. C.
- 16. the process of claim 15, comprising impregnation with 1-6% by weight, relative to the total weight of the catalyst, of one or more alkali metal hydroxides after the activation.
- 17. The process of claim 15, wherein the activating treatment with hydrogen is not carried out until directly before the catalyst is used in the reactor intended for this purpose.
Priority Claims (1)
Number |
Date |
Country |
Kind |
3840194 |
Nov 1988 |
DEX |
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Parent Case Info
This is a division of application Ser. No. 07/433,874, filed Nov. 9, 1989, now abandoned.
US Referenced Citations (6)
Foreign Referenced Citations (3)
Number |
Date |
Country |
0146534 |
Sep 1983 |
JPX |
0493339 |
Oct 1938 |
GBX |
1413949 |
Nov 1975 |
GBX |
Divisions (1)
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Number |
Date |
Country |
Parent |
433874 |
Nov 1989 |
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