Process for the preparation of salts of 1-substituted...

Details Process for the preparation of salts of 1-substituted... Process for the preparation of salts of 1-substituted...

2000-04-11

2001-03-20

Barts, Samuel (Department: 1621)

Organic compounds -- part of the class 532-570 series

Organic compounds

Amino nitrogen containing

C564S420000, C564S421000, C564S422000, C564S423000

Reexamination Certificate

active

06204413

ABSTRACT:

BACKGROUND OF THE INVENTION
The present invention relates to a process for the preparation of salts of 1-substituted 2,4-diaminobenzenes by catalytic hydrogenation of the corresponding 1-substituted 2,4-dinitrobenzenes and conversion of the resulting reaction product, following removal of the catalyst, into the salt form.
Salts of 1-substituted 2,4-diaminobenzenes are used in many different areas. Their synthesis is therefore of particular importance. 2-(2′,4′-diamino-diaminophenoxy)-ethanol and its salts are used, for example, according to DE-A-27 58 735 and DE-A-27 37 138, in oxidation dye compositions as the meta-component.
DE-A-27 58 735 describes the preparation of 2-(2′,4′-diaminophenoxy)-ethanol by catalytic hydrogenation of 2-(2′,4′-dinitrophenoxy)-ethanol. To remove the catalyst, the reaction mixture after the hydrogenation is filtered in the warmed state, and the filtrate is recovered. To prepare the dihydrochloride salt of 2-(2′,4′-diaminophenoxy)-ethanol, an excess of hydrogen chloride gas is then introduced into the filtrate. However, this method produces a yield of only 78%. Reworking this process also shows that the product is produced in a deep violet color and contains considerable amounts of by-products and decomposition products, which is manifested in a purity of only 86%. Measurement of the degrees of transmission of a 0.1% strength solution of the product in water according to DIN 55945 gives the results T
x
=38.6, T
y
=26.4 and T
z
=30.9.
Particularly when the salts of the 1-substituted 2,4-diaminobenzenes, such as 2-(2′,4′-diaminophenoxy)-ethanol, are used in the cosmetics sector, e.g., as precursor compounds in the field of hair cosmetics, the purity of the 1-substituted 2,4-diaminobenzenes is a decisive factor: even slight contamination by foreign substances is problematical for medicinal reasons (e.g., danger of triggering allergies).
The object of the present invention was therefore to provide a process with which salts of 1-substituted 2,4-diaminobenzenes and in particular of 2-(2′,4′-diaminophenoxy)-ethanol can be obtained with low impurities and low undesired discoloration.
DESCRIPTION OF THE INVENTION
The above-mentioned object is achieved by a process for the preparation of salts of 1-substituted 2,4-diaminobenzenes of the formula (I)
wherein each R
1
is a linear or a branched C
1
-C
20
-alkyl group, a C
6
-C
18
-aryl group, a C
2
-C
20
-acyl group, a COOH group, a COOR
3
group in which R
3
is a linear or a branched C
1
-C
20
-alkyl radical, or N(R
4
)
2
, in which each R
4
is hydrogen, a linear or a branched C
1
-C
20
-alkyl radical or a C
2
-C
20
-acyl radical, and n is an integer from 0 to 3,
R
2
is a radical of the formula (II)
in which each R
5
is hydrogen or a C
1
-C
5
-alkyl radical, m is an integer from 1 to 12 and p is an integer from 1 to 4, or a radical of the formula (III),
in which r is an integer from 0 to 2 and optionally one or more carbon atoms of the phenyl ring are replaced by N, O or S, and Y
⊖
is the equivalent amount of a monovalent, divalent, or a trivalent anion.
Generally, the process involves the step of catalytically hydrogenating 1-substituted 2,4-dinitrobenzenes of the formula (IV),
in which R
1
, n and R
2
have the meanings given for formula (I), and separating the reaction product obtained, after the hydrogenation, from the catalyst and adding the reaction product to an aqueous solution of an acid H
⊕
Y
⊖
, in which Y
⊖
has the meaning given above. The process according to the invention is characterized in that the product of the formula (I) can be obtained in an excellent yield of at least 80%, preferably at least 85%, particularly preferably at least 89%, and also with a very high purity of up to 98% and an improved color.
In the 1-substituted 2,4-dinitrobenzenes of the formula (IV), each R
1
is preferably a linear or a branched C
1
-C
10
-alkyl group, a C
6
-C
12
-aryl group, a C
2
-C
6
-acyl group or a N(R
4
)
2
group in which each R
4
is hydrogen, a linear or a branched C
1
-C
6
-alkyl radical or a C
2
-C
6
-acyl radical. In addition, n is preferably an integer from 0 to 2.
R
2
is preferably a radical of the formula (II) in which m is an integer from 1 to 9, in particular 1, 2 or 3, R
5
is hydrogen or methyl, and p is 1 or 2. Particularly preferably, the radical R
2
is —[CH
2
—CH
2
]—, —[CH(CH
3
)—CH
2
]— or —[CH
2
—C(CH
3
)
2
—CH
2
]—, where p is 1.
In addition, R
2
is preferably a radical of the formula (III), where r is 0 or 1. Particularly preferably, the radical R
2
is,
In particular, the process according to the invention has proven successful for preparing the salts of 2-(2′,4′-diaminophenoxy)-ethanol from 2-(2′,4′-dinitrophenoxy)-ethanol, where Y
⊖
is preferably Cl
⊖
,
½
(SO
4
)
2⊖
or ⅓(PO
4
)
3⊖
.
A process for the preparation of 1-substituted 2,4-dinitrobenzenes of the formula (IV) is described in a German Patent Application filed on the same date. Other processes are known from DE-A-27 58 735, J. Chem. Soc. 1921 (119), 2076-8 and U.S. Pat. No. 2,988,571.
The hydrogenation of the 1-substituted 2,4-dinitrobenzenes according to formula (IV) is carried out in the presence of hydrogenation catalysts, which are sufficiently known to the person skilled in the art. Examples of such catalysts include noble metal catalysts based on platinum or palladium. It is also possible to use Raney nickel or Raney cobalt catalysts, which can, if appropriate, be alloyed with other metals such as molybdenum, titanium, vanadium, magnesium, iron or chromium. The hydrogenation catalysts can be supported or unsupported.
The hydrogenation is generally carried out in the presence of a solvent. Examples of suitable solvents are branched or unbranched aliphatic alcohols, preferably isopropanol, and optionally substituted aromatic hydrocarbons such as toluene or chloroaromatics. The hydrogenation is generally carried out at a hydrogen pressure of 0.1 to 10 MPa, preferably 0.5 to 5 MPa and at a temperature of 20 to 150° C., preferably 40 to 120° C.
The reaction product obtained after the hydrogenation of the 1-substituted 2,4-dinitrobenzenes of the formula (IV) is separated from the catalyst and is introduced into an aqueous solution of an acid H
⊕
Y
⊖
, in which Y
⊖
is the equivalent amount of a monovalent, divalent or trivalent basic acid anion.
The acid H
⊕
Y
⊖
is preferably hydrochloric acid, sulphuric acid or phosphoric acid, e.g, Y
⊖
is Cl
⊖
,
½
(SO
4
)
2⊖
or ⅓(PO
4
)
3⊖
. The acid H
⊕
Y
⊖
is introduced in an amount such that the molar ratio of the acid H
⊕
Y
⊖
, to the reaction product of the hydrogenation, i.e., the 1-substituted 2,4-diamino-benzene, is at least 2:1.
It has also proven successful to add the reaction product obtained after the hydrogenation and separated from the catalyst to an initial charge which includes not only the aqueous solution of the acid H
⊕
Y
⊖
, but also a solvent which is miscible with the acid H
⊕
Y
⊖
water. Preference is given to using isopropanol as such a solvent. As a result, a further increase in the yield can be achieved. It has proven successful to carry out the reaction using an inert gas.
The invention provides numerous advantages. For instance, unlike the process in DE-A-27 58 735 discussed in the Background of the Invention) the present invention avoids the low yields obtained by this process as well as avoids the deep violet color containing considerable amounts of by-products and decomposition products. As such, the invention provides a valuable process for preparing an important class of compounds.


REFERENCES:
patent: 2988571 (1961-06-01), MacFie et al.
patent: 4125367 (1978-11-01), Bugaut et al.
patent: 4259261 (1981-03-01), Bugaut et al.
patent: 4329504 (1982-05-01), Bugaut et al.
patent: 4854935 (1989-08-0

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