Process for the preparation of chloro-benzoyl chlorides

Abstract

An effective and efficient process for the preparation of chloro-benzoylchlorides of formula I, ##STR1## (n is defined in the specification). In this process a a chloro-trichloromethylbenzene of formula II ##STR2## is treated with water acid in the presence of a Lewis at temperatures below 80.degree. C. The compounds obtained according to this process can be used to prepare certain chloro-substituted benzophenones.

Description

BACKGROUND OF THE INVENTION

The present invention relates to a process for the preparation of chloro-benzoylchlorides from a chloro-trichloromethylbenzene in which said chloro-trichloromethylbenzene is treated with water in the presence of a Lewis acid at temperatures below 80.degree. C.

Chloro-trichloromethylbenzene compounds are suitable intermediates for the preparation of a broad variety of compounds which are useful as agrochemicals, pharmaceuticals or liquid crystals. In particular, they are key intermediates in the preparation of fungicidal dimethomorph (e.g. EP 0 120 321) and fungicidal benzophenones which are described for example in EP 0 727 141 A.

The German patent no. 331696 (Jul. 17, 1914) discloses a process wherein trichloromethylbenzene is treated with equimolar amounts of water in the presence of FeCl.sub.3 at elevated temperatures to form benzoylchloride.

However, this process is hardly applicable in technical scale since it causes problems with respect to the dosing rate and the exact equimolar dosing of water at elevated temperatures. Any excess of water will cause hydrolysis of the desired acid chloride compound and therefore reduce the yields.

SUMMARY OF THE INVENTION

The present invention provides an effective and efficient process for the preparation of chloro-benzoylchlorides of formula I, ##STR3## wherein n represents an integer of 1, 2 or 3,

from a chloro-trichloromethylbenzene of formula II ##STR4## wherein n has the meaning given, the improvement wherein is that the trichloromethylarene is treated with water acid in the presence of a Lewis acid at temperatures below 80.degree. C.

It is, therefore, an object of the present invention to provide an efficient new process for the preparation of chloro-benzoylchloride compounds.

Other objects and advantages of the present invention will be apparent to those skilled in the art from the following description and the appended claims.

DETAILED DESCRIPTION OF THE INVENTION

Further preferred embodiments of the process according to the present invention is a process wherein:

the reaction is carried out without organic solvent; the Lewis is FeCl.sub.3, the reaction mixture essentially consisting of the chloro-trichloromethylbenzene of formula II and the Lewis acid is heated up to temperatures below 80.degree. C. and water is slowly added into the stirred solution; the chloro-trichloromethylbenzene is a mono- or dichloro-trichloromethylbenzene, in particular 4-chloro-trichloromethylbenzene or 2,6-dichloro-trichloromethylbenzene; 1 mole of trichloromethylarene of formula II is treated with 0.8 to 1.2, preferably 0.9 to 1.1, in particular about 1 moles of water; 1 mole of trichloromethylarene of formula II is treated with water in the presence of 0.05 to 5 mol-%, preferably 0.1 to 3 mol-% of the Lewis acid.

The reaction is carried out at a temperature between ambient temperature and 80.degree. C., preferably between 40 and 80.degree. C., in particular between 45 and 65.degree. C.

As a rule the reaction can be carried out under reduced or elevated pressure, preferably it is carried out under atmospheric pressure.

In a particularly preferred embodiment of the process according to the invention 1 equivalent of 4-chloro-trichloromethylbenzene, is mixed with 0.1 to 3 mol-% of the Lewis acid, in particular FeCl.sub.3 and heated to 45 to 65.degree. C., in particular 50 to 60.degree. C. Then about 1 equivalent of water is dosed into this reaction mixture, which is kept at this temperature. The hydrochloric acid formed during the reaction is evolved out until the reaction is completed.

Under this preferred reaction conditions the reaction is as a rule completed within 0.25 to 5, in particular 1 to 4 hours.

The remaining aroyl chloride can be used as intermediate for the preparation of the desired end-products without further purification. In a particularly preferred embodiment the reaction mixture obtained can be used for the preparation of certain chloro-substituted benzophenone derivatives under Friedel-Crafts acylation conditions, in particular of formula III, ##STR5## in which n has the meaning given, and

R each independently represents C.sub.1-6 alkyl or C.sub.1-6 alkoxy, and m is an integer from 2 to 4,

under Friedel-Crafts acylation conditions by adding a Lewis acid and the corresponding substituted benzene derivative, preferably of formula IV, ##STR6##

in particular 1,2-dimethoxybenzene, 3,4,5-trimethoxytoluene or 3,4-dimethoxy-5-butoxytoluene, to said reaction mixture.

It is also possible to purify the obtained chloro-benzoylchlorides using standard procedures, as for example crystallization or distillation, in particular by distillation under reduced pressure, in particular at pressures between 1 and 100 mbar.

The novel process enables to carry out the production of chloro-benzoyl chlorides in technical scale and high yields using cheap, ready-available educts.

In order to facilitate a further understanding of the invention, the following illustrative examples are presented. The invention is not limited to the specific embodiments described or illustrated, but encompasses the full scope of the appended claims.

EXAMPLE 1

Preparation of 4-chlorobenzoylchloride (PCBO)

A mixture of 115 g 4-chlorobenzotrichloride (CBTC, 0.5 mol) and 1.6 g FeCl.sub.3 (10 mmol) is heated to 60.degree. C. 9 g water (0.5 mol) are dosed into the mixture within 1 hours at ambient pressure. After 30 minutes the reaction was complete; the GC analysis showed that the conversion was complete (98 area-% PCBO). In order to determine the yield, the corresponding methyl-ester has been made by adding 1.5 equivalent methanol to the obtained product. The resulting mixture was solved in toluene and washed with 5% aquaous HCl and water. After removing the solvent and recrystalization 83.3 g p-chloromethylbenzoate (98% purity) was formed. Total yield 93%.

EXAMPLE 2

Preparation of 4-chlorobenzoylchloride (PCBO)

A mixture of 460 g 4-chlorobenzotrichloride (CBTC, 2 mol) and 6.5 g FeCl.sub.3 (20 mmol) is heated to 50.degree. C. 36 g water (2 mole) are dosed into the mixture within 2 hours at ambient pressure. After 30 minutes the reaction was complete; the GC analysis showed that the conversion was complete (>95 area-% PCBO).

The results of further experiments are given in the following table, in which the conversions have been determined by GC analysis:

TABLE 1______________________________________GC-Area % PCBO of mixture CBTC FeCl.sub.3 GC-area % (mol) (mol %) T (.degree. C.) PCBO______________________________________1,5 2 53 97 2 2 51 97 2 2 60 98______________________________________ In the following eperiments the yield of PCBO has been determined as the actual content of the product given in weight % as shown in Table 2: TABLE 2______________________________________Weight % PCBO of mixture CBTC FeCl.sub.3 weight % (mol) (mol %) T (.degree. C.) PCBO______________________________________2 0.5 50 94.2 2 0.25 50 95.3______________________________________

COMPARISON EXAMPLE

Preparation of 4-chloro-benzoylchloride

A mixture of 460 g 4-chlorobenzotrichloride (CBTC, 2 mol) and 1.0 g FeCl.sub.3 (3.08 mmol) is heated to 100.degree. C. 36 g water (2 mol) are dosed into the mixture within 2 hours at ambient pressure. After 30 minutes the analysis showed that the conversion was incomplete (85 weight % PCBO).

Claims

1. In an improved process for the preparation of chloro-substituted benzophenone derivatives of formula III, ##STR7## in which n represents an integer of 1, 2 or 3,

R each independently represents C.sub.1-6 alkyl or C.sub.1-6 alkoxy, and

m is an integer from 2 to 4,

from a chloro-trichloromethylbenzene of formula II ##STR8## wherein n has the meaning given, the improvement comprising the steps of

(a) treating the trichloromethylarene of formula II with water in the presence of a Lewis acid at temperatures below 80.degree. C. to obtain a reaction mixture comprising a chloro-benzoylchloride of formula I ##STR9## wherein n has the meaning given, and (b) adding a substituted benzene derivative of formula IV, ##STR10## and optionally a Lewis acid to the said reaction mixture and treating the resulting reaction mixture under Friedel-Crafts acylation conditions.

2. A process according to claim 1, wherein the Lewis acid is FeCl.sub.3.

3. A process according to claim 1, wherein in step (a) 1 mole of chloro-trichloromethylbenzene of formula II is treated with 0.8 to 1.2 moles of water.

4. A process according to claim 1, wherein in step (a) 1 mole of trichloromethylarene of formula II is treated with water in the presence of 0.02 to 5.0 mol-% of the Lewis acid.

5. A process according to claim 1, wherein in step 1 about 1 equivalent of water is slowly dosed into a mixture essentially consisting of 1 equivalent of chloro-trichloromethylbenzene of formula II and 0.05 to 3.0 mol-% of the Lewis acid at 40 to 80.degree. C.

6. A process according to claim 1, wherein in step (b) the compound of formula IV is selected from 1,2-dimethoxybenzene, 3,4,5-trimethoxytoluene and 3,4-dimethoxy-5-butoxytoluene.