Method for producing substituted nitro benzoic acids by oxidation of corresponding nitro toluenes, nitrol benzyl alcohols, esters and/or ethers
View Patent ↗The present invention relates to the preparation of nitrobenzoic acids by oxidizing particular nitrotoluenes, nitrobenzyl alcohols, esters and/or ethers in the presence of nitric acid at elevated temperature and elevated pressure. It has been found that the particular nitrotoluenes, nitrobenzyl alcohols, esters and/or ethers may be oxidized particularly reliably and in high yields using nitric acid to the benzoic acid derivatives when they are metered into the nitric acid.
1. A process for preparing nitrobenzoic acids of the general formula (I)
where
each X is independently nitro, cyano, sulfonyl, carboxyl, carbonylphenyl, trifluoromethyl or trichloromethyl,
each Y is independently phenyl, fluorine, chlorine, bromine or iodine and the phenyl radical, optionally substituted by up to 3 X and/or Y radicals other than hydrogen,
m has the value 0, 1, 2 or 3 and
n has the value 0, 1, 2 or 3,
and the sum of m and n has the value 0, 1, 2, 3 or 4,
from compounds of the general formula (II)
where
X, Y, m, n and also the sum of n and m are each as defined above for the general formula (I) and
R is H or an OR′ radical and
R′ is H, straight-chain or branched C 1 -C 10 -alkyl or straight-chain or branched C 1 -C 10 -carbonylalkyl or R′ is a radical of the general formula (III)
or a radical of the general formula (IV),
where X, Y, n, m, and the sum of n and m are each as defined for the general formula (I),
comprising heating a mixture of nitric acid and water at a pressure in the range of 2-20 bar at temperatures in the range of 100-220° C. and metering the compound of the general formula (II) into the heated mixture of nitric acid and water,
with the proviso that compounds of the general formula (II) exclude 2-halo-6-nitrobenzyl alcohols, esters or ethers of the general formula (V) and
where
R′ is as defined for the general formula (II),
R 1 , R 2 and R 3 are each independently H, fluorine, chlorine, bromine, nitro or carboxyl and
Hal is fluorine, chlorine or bromine;
wherein the maximum concentration of the compound of the general formula (II) in the reaction mixture as 7% by weight.
2. The process of claim 1 , wherein the maximum concentration of the compound of the general formula (II) in the reaction mixture is 6% by weight.
3. The process of claim 1 , wherein the maximum concentration of the compound of the general formula (II) in the reaction mixture is 5% by weight.
4. A process for preparing nitrobenzoic acids of the general formula (I)
where
each X is independently nitro, cyano, sulfonyl, carboxyl, carbonylphenyl, trifluoromethyl or trichloromethyl,
each Y is independently phenyl, fluorine, chlorine, bromine or iodine and the phenyl radical, optionally submitted by up to 3 X and/or Y radicals other than hydrogen,
wherein n has the value 0, 1 or 2 and m has the value 0, 1 or 2, and the sum of n and m has the value 1 or 2,
from compounds of the general formula (II)
where
X, Y, m, n and also the sum of n and m are each as defined above for the general formula (I) and
R is H or an OR′ radical and
R′ is H, straight-chain or branched C 1 -C 10 -alkyl or straight-chain or branched C 1 -C 10 -carbonylalkyl or R′ is a radical of the general formula (III)
or a radical of the general formula (IV),
where X, Y, n, m, and the sum of n and m are each as defined for the general formula (I),
comprising heating a mixture of nitric acid and water at a pressure in the range of 2-20 bar at temperatures in the range at 100-220° C. and metering the compound of the general formula (II) into the heated mixture of nitric acid and water,
with the proviso that compounds of the general formula (II) exclude 2-halo-6-nitrobenzyl alcohols, esters or ethers of the general formula (V) where
R′ is as defined for the general formula (II),
R 1 , R 2 and R 3 are each independently H, fluorine, chlorine, bromine, nitro or carboxyl and
Hal is fluorine, chlorine or bromine.
5. A process for preparing 2-carboxy-5-nitrobenzenesulfonic acid, comprising heating a mixture of nitric acid and water at a pressure in the range of 2-20 bar at temperatures in the range of 100-220° C. and metering 4-nitrotoluene-2-benzenesulfonic acid into the heated mixture of nitric acid and water.
6. A process for preparing nitrobenzoic acids of the general formula (I)
where
each X is independently nitro, cyano, sulfonyl, carboxyl, carbonylphenyl, trifluoromethyl or trichloromethyl,
each Y is independently phenyl, fluorine, chlorine, bromine or iodine and the phenyl radical, optionally substituted by up to 3 X and/or Y radicals other then hydrogen,
m has the value 0, 1, 2 or 3 and
n has the value 0, 1, 2 or 3,
and the sum of m and n has the value 0, 1, 2, 3 or 4,
from compounds of the general formula (II)
where
X, Y, m, n and also the sum of n and m are each defined above for the general formula (I) and
R is H or an OR′ radical and
R is H, straight-chain or branched C 1 -C 10 -alkyl or straight-chain or branched C 1 -C 10 -carbonylalkyl or R′ is a radical of the general formula (III)
or a radical of the general formula (IV),
where X, Y, n, m, and the sum of n and m are each as defined for the general formula (I),
comprising heating a mixture of nitric acid and water at a pressure in the range of 4-15 bar at a temperatures in the range of 120-200° C. and metering the compound of the general formula (II) into the heated mixture of nitric acid and water,
with the proviso that compounds of the general formula (II) exclude 2-halo-6-nitrobenzyl alcohols, esters or ethers of the general formula (V) and
where
R′ is as defined for the general formula (II),
R 1 , R 2 and R 3 are each independently H, fluorine, chlorine, bromine, nitro or carboxyl and
Hal is fluorine, chlorine or bromine.
7. The process of claim 6 , wherein process is carried out at a pressure of 10-12 bar and at a temperature of 120-200° C.
8. The process as claimed in claim 6 , wherein the process is carried out at a pressure ranging from 6 to 12 bar and at a temperature of 140 to 180° C.
9. The process as claimed in claim 6 , wherein the process is carried out at a pressure ranging from 10 to 12 bar and at a temperature of 140 to 180° C.
10. The process as claimed in claim 6 , wherein the process is carried out at a pressure ranging from 4 to 15 bar and at a temperature of 140 to 180° C.
11. The process of claim 6 , wherein the process as claimed in claim 1 carried out at a pressure of 6 to 12 bar and at a temperature of 120-200° C.
12. A process for preparing nitrobenzoic acids of the general formula (I)
where
each X is independently nitro, cyano, sulfonyl, carboxyl, carbonylphenyl, trifluoromethyl or trichloromethyl,
each Y is independently phenyl, fluorine, chlorine, bromine or iodine and the phenyl radical, optionally substituted by up to 3 X and/or Y radicals other than hydrogen,
m has the value 0, 1, 2 or 3 and
n has the value 0, 1, 2 or 3,
and the sum of m and n has the value 0, 1, 2, 3 or 4,
from compounds of the general formula (II)
where
X, Y, m, n and also the sum of n and m are each as defined above for the general formula (I) and
R is H or an OR′ radical and
R′ is H, straight-chain or branched C 1 -C 10 -alkyl or straight-chain or branched C 1 -C 10 -carbonylalkyl or R′ is a radical of the general formula (III)
or a radical of the general formula (IV),
where X, Y, n, m, and the sum of n and m are each as defined for the general formula (I),
comprising heating a mixture of nitric acid and water at a pressure in the range of 2-20 bar at temperatures in the range of 100-220° C. and metering the compound of the general formula (II) into the heated mixture of nitric acid and water,
with the proviso that compounds of the general formula (II) exclude 2-halo-6-nitrobenzyl alcohols, esters or ethers of the general formula (V) and
where
R′ is as defined for the general formula (II),
R 1 , R 2 and R 3 are each independently H, fluorine, chlorine, bromine, nitro or carboxyl and
Hal is fluorine, chlorine or bromine;
wherein the molar ratio of the compound of the general formula (II) to nitric acid is in the range of (2-20):1.
13. The process as claimed in claim 12 , wherein the molar ratio of the compound of the general formula (II) to nitric acid is in the range of (3-10):1.
14. The process as claimed in claim 12 , wherein the molar ratio of the compound of the general formula (II) to nitric acid is in the range of (4-8):1.
15. A process for preparing nitrobenzoic acids of the general formula (I)
where
each X is independently nitro, cyano, sulfonyl, carboxyl, carbonylphenyl, trifluoromethyl or trichloromethyl,
each Y is independently phenyl, fluorine, chlorine, bromine or iodine and the phenyl radical, optionally substituted by up to 3 X and/or Y radicals other than hydrogen,
m has the value 0, 1, 2 or 3 and
n has the value 0, 1, 2 or 3,
and the sum of m and n has the value 0, 1, 2, 3 or 4,
from compounds of the general formula (II)
where
X, Y, m, n and also the sum of n and m are each as defined above for the general formula (I) and
R is H or an OR′ radical and
R′ is H, straight-chain or branched C 1 -C 10 -alkyl or straight-chain or branched C 1 -C 10 -carbonylalkyl or R′ is a radical of the general formula (III)
or a radical of the general formula (IV).
where X, Y, n, m, and the sum of n and m are each as defined for the general formula (I),
comprising heating a mixture of nitric acid and water at a pressure in the range of 2-20 bar at temperatures in the range of 100-220° C. and metering the compound of the general formula (II) into the heated mixture of nitric acid and water,
with the proviso that compounds of the general formula (II) exclude 2-halo-6-nitrobenzyl alcohols, esters or ethers of the general formula (V) and
where
R′ is as defined for the general formula (II),
R 1 , R 2 and R 3 are each independently H, fluorine, chlorine, bromine, nitro or carboxyl and
Hal is fluorine, chlorine or bromine;
wherein 10%-20% of the nitric acid is used initially charged and heated, and then the compound of the general formula (II) and the remaining nitric acid are metered into the reactor simultaneously and separately.
16. A process for preparing nitrobenzoic acids of the general formula (I)
where
each X is independently nitro, cyano, sulfonyl, carboxyl, carbonylphenyl, trifluoromethyl or trichloromethyl,
each Y is independently phenyl, fluorine, chlorine, bromine or iodine and the phenyl radical, optionally substituted by up to 3 X and/or Y radicals other than hydrogen,
m has the value 0, 1, 2 or 3 and
n has the value 0, 1, 2 or 3,
and the sum of m and n has the value 0, 1, 2, 3 or 4,
from compounds of the general formula (II)
where
X, Y, m, n and also the sum of n and m are each as defined above for the general formula (I) and
R is H of an OR′ radical and
R′ is H, straight-chain or branched C 1 -C 10 -alkyl or straight-chain or branched C 1 -C 10 -carbonylalkyl or R′ is a radical of the general formula (III)
or a radical of the general formula (IV),
where X, Y, n, m, and the sum of n and m are each as defined for the general formula (I),
comprising heating a mixture of nitric acid and water at a pressure in the range of 2-20 bar at temperatures in the range of 100-220° C. and metering the compound of the general formula (II) into the heated mixture of nitric acid and water,
with the proviso that compounds of the general formula (II) exclude 2-halo-6-nitrobenzyl alcohols, esters or ethers of the general formula (V) and
where
R′ is as defined for the general formula (II),
R 1, R 2 and R 3 are each independently H, fluorine, chlorine, bromine, nitro or carboxyl and
Hal is fluorine, chlorine or bromine;
wherein from 20 to 50% of the nitric acid used is initially charged and heated, and then the compound of the general formula (II) and the remaining nitric acid are metered into the reactor simultaneously and separately.
17. A process for preparing nitrobenzoic acids of the general formula (I)
where
each X is independently nitro, cyano, sulfonyl, carboxyl, carbonylphenyl, trifluoromethyl or trichloromethyl,
each Y is independently phenyl, fluorine, chlorine, bromine or iodine and the phenyl radical, optionally substituted by up to 3 X and/or Y radicals other than hydrogen,
m has the value 0, 1, 2 or 3 and
n has the value 0, 1, 2 or 3,
and the sum of m and n has the value 0, 1, 2, 3 or 4,
from compounds of the general formula (II)
where
X, Y, m, n and also the sum of n and m are each as defined above for the general formula (I) and
R is H or an OR′ radical and
R′ is H, straight-chain or branched C 1 -C 10 -alkyl or straight-chain or branched C 1 -C 10 -carbonylalkyl or R′ is a radical of the general formula (III)
or a radical of the general formula (IV),
where X, Y, n, m, and the sum of n and m are each as defined for the general formula (I),
comprising heating a mixture of nitric acid and water at a pressure in the range from 2 to 20 bar at temperatures in the range of 100-220° C. and metering the compound of the general formula (II) unto the heated mixture of nitric acid and water,
with the proviso that compounds of the general formula (II) exclude 2-halo-6-nitrobenzyl alcohols, esters or ethers of the general formula (V) and
where
R′ is as defined for the general formula (II),
R 1 , R 2 and R 3 are each independently H, fluorine, chlorine, bromine, nitro or carboxyl and
Hal is fluorine, chlorine or bromine;
wherein alkali metal or alkaline earth metal nitrites, nitrous acid or concentrated red-brown nitric acid are added to the nitric acid which release or contain NO x .