EP0569377A1

EP0569377A1 - Process for producing 4h-3,1-benzoxazine-t-ones

Info

Publication number: EP0569377A1
Application number: EP19920901610
Authority: EP
Inventors: Erwin Hahn; Paul Guenthert; Guenther Glas
Original assignee: BASF SE
Current assignee: BASF SE
Priority date: 1991-01-18
Filing date: 1992-01-08
Publication date: 1993-11-18
Also published as: JPH06504532A; DE4101380A1; WO1992012971A1; CA2100562A1

Abstract

Production de 4H-3,1-benzoxazin-4-ones de formule (I), dans laquelle R1 représente hydrogène, alkyle C1-C4, alcoxy C1-C4, carboxyle, sulfo, nitro ou halogène; R2 représente alkyle C1-C20, phényle ou phénylalkyle ayant 1 à 4 atomes de carbone dans le groupe alkyle, un noyau phényle présent pouvant être substitué par un ou deux groupes alkyle C1-C4, groupes alkyle C1-C3; groupes alcoxy C1-C4, groupes alcoxy halogène C1-C4, groupes alkylmercapto C1-C4, groupes alkylmercapto halogène C1-C3, groupes carboxyle, groupes sulfo, groupes alkylsulfonyle C1-C4, groupes alkylsulfonyle halogène C1-C3, groupes nitro ou atomes d'halogène; et n vaut 1 ou 2; par la mise en réaction d'anhydrides d'acide isato de formule (II) avec des haloïdes acyle de formule (III) dans laquelle X représente chlore ou brome. La mise en réaction s'effectue à une température extérieure de 215 à 280 °C et les composants de la réaction (II et III) sont laissés en réaction pendant au moins 4 heures à cette température.Production of 4H-3,1-benzoxazin-4-ones of formula (I), in which R1 represents hydrogen, C1-C4 alkyl, C1-C4 alkoxy, carboxyl, sulfo, nitro or halogen; R2 represents C1-C20 alkyl, phenyl or phenylalkyl having 1 to 4 carbon atoms in the alkyl group, a phenyl ring present may be substituted by one or two C1-C4 alkyl groups, C1-C3 alkyl groups; C1-C4 alkoxy groups, C1-C4 halogen alkoxy groups, C1-C4 alkylmercapto groups, C1-C3 halogen alkylmercapto groups, carboxyl groups, sulfo groups, C1-C4 alkylsulfonyl groups, C1-C3 halogenated alkylsulfonyl groups, nitro groups or d atoms 'halogen; and n is 1 or 2; by reacting isato acid anhydrides of formula (II) with acyl haloids of formula (III) in which X represents chlorine or bromine. The reaction takes place at an outside temperature of 215 to 280 ° C and the reaction components (II and III) are left to react for at least 4 hours at this temperature.

Description

Process for the preparation of 4H-3,1-benzoxazin-4-ones

description

The present invention relates to an improved process for the preparation of 4H-3,1-benzoxazin-4-ones of the general formula I.

in which R ¹ denotes hydrogen, C ₁ -C ₄ alkyl, C ₁ -C ₄ alkoxy, carboxyl, sulfo, nitro or halogen,

R ^{2 is} C ₁ -C ₂₀ alkyl, phenyl or phenylalkyl having 1 to 4 C atoms in the alkyl group, a phenyl nucleus being represented by one or two C ₁ -C ₄ alkyl groups, C ₁ -C ₃ haloalkyl groups, C ₁ -C ₄ alkoxy groups, C ₁ -C ₃ haloalkoxy groups, C ₁ -C ₄ alkyl mercapto groups, C ₁ -C ₃ haloalkyl mercapto groups, carboxyl groups, sulfo groups, C ₁ -C ₄ alkylsulfonyl groups, C ₁ -C ₃ haloalkyl sulfonyl groups , Nitro groups or halogen atoms can be substituted, and n represents 1 or 2, by reaction of isatoic anhydrides of the general

Formula II

with acyl halides of the general formula III

where X denotes chlorine or bromine. In the references J. Prakt. Chemie, Vol. 30 (1884),

Pp. 484-487, and vol. 33 (1886), pp. 18-31, describe E. v. Meyer and Th. Bellmann described a process for the preparation of "benzoylanthranil" (2-phenyl-4H-3,1-benzoxazin-4-one) by heating unsubstituted isatoic anhydride (incorrectly referred to there as isatoic acid) with excess benzoyl chloride at the boil or "im closed pipe "at 210 ° C. The implementation is marked as incomplete ("a lot of unchanged isato acid separates out of the solution, to which benzoylanthrani1 is added"). No details are given on the reaction time, batch size, stoichiometry of the starting materials or yield.

DE-A 35 14 183 relates to a process for the preparation of optionally substituted 2-phenyl-4H-3,1-benzoxazin-4-ones by reacting a corresponding anthranic acid with a corresponding benzoyl halide in the presence of a base

(Acylation) and ring closure by dehydration (cyclization). DE-AS 25 56 590 describes a process for the preparation of benzoxazines, especially 2-alkyl- or 2-aryl-4H-3,1-benzoxazin-4-ones, in which an isatoic anhydride with an acylating agent in the form a carboxylic acid anhydride or an acid halide is reacted in the presence of effective portions of a tertiary amine.

However, all of the processes mentioned are not yet satisfactory from an economic point of view, be it that the yields are still too low, or be it that complicated, multistage reaction paths have to be followed or that expensive auxiliary chemicals have to be used.

The object of the present invention was therefore to provide a simple, efficient and economical process for the preparation of the 4H-3,1-benzoxazin-4-one I.

Accordingly, the process defined at the outset has been found, which is characterized in that the reaction is carried out at an outside temperature of 215 to 280 ° C. and the reactants II and III are allowed to react with one another at this temperature for at least 4 hours. In a preferred embodiment, the outside temperature for the reaction is 220 to 250 ° C. The outside temperature is to be understood as the temperature of the jacket of the reaction vessel, in particular of the heating liquid located in this jacket.

The inside temperature, i.e. the temperature of the reaction mixture itself should ideally be identical to the outside temperature; in practice, however, the inside temperature is usually a few degrees lower than the outside temperature. It should also be noted that when using an acyl halide III, the boiling point of which is lower than the temperature range claimed for the reaction according to the invention, the internal temperature is equal to the boiling temperature of III towards the start of the reaction (for example 197 ° C. when using benzoyl chloride), with decrease the

Concentration of free acyl halide III in the reaction mixture but the internal temperature quickly increases towards the value of the set external temperature. The reaction time for the temperature range mentioned is at least 4 hours, after which a conversion of 80 to 95% is normally achieved. However, it is cheaper to let the implementation run for at least 5 hours, because after this time the turnover is usually 95% or higher. After 6 hours of reaction, the reaction is usually practically complete.

The reaction is advantageously carried out at normal pressure. Working in closed reaction vessels under autogenous pressure or in autoclaves at elevated pressures is not necessary; this is questionable for safety reasons, because during the reaction gases (hydrogen chloride and carbon dioxide) are released that have to be removed. 1.0 to 1.5 mol of acyl halide II is used per mol of isatoic anhydride II. A larger excess of III often leads to the reaction mixture not reaching the temperature required for rapid reaction. An amount of 1.0 to 1.3 mol III, in particular 1.05 to 1.2 mol III, per mol II is particularly favorable. Acyl halides III are acyl bromides (X = Br) and especially acyl chlorides (X = Cl).

As residues R ¹ , which can be in the 5-, 6-, 7- and / or 8-position on the benzene nucleus of the heterocyclic system, are added

Hydrogen into consideration: - C ₁ -C ₄ alkyl groups such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec.-butyl and tert.-butyl, - C ₁ - to C ₄ Alkoxy groups such as methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, iso-butoxy, sec.-butoxy, tert-butoxy and methylenedioxy, - carboxyl groups, which should expediently be in the form of free acids, - sulfo groups, which expediently as free acids

should be available

- Nitro groups and - Halogen atoms such as fluorine, chlorine and bromine. For Ri, methyl groups, methoxy groups, halogen atoms and in particular hydrogen alone are preferred.

The number n of the radicals R ¹ is 2 or preferably 1. The radicals R ² in the 2-position of the benzoxazin-4-one system are: straight-chain or branched C ₁ -C ₂₀ -alkyl, for example methyl, ethyl, n-propyl, iso-propyl, n-butyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, iso¬

Nonyl, n-decyl, n-undecyl, n-dodecyl, n-tridecyl, iso-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl or n-eicosyl, Pheny l and

Phenylalkyl with 1 to 4 carbon atoms in the alkyl group, e.g.

Benzyl, 2-phenylethyl, 3-phenylpropyl or 4-phenyl butyl.

An existing phenyl nucleus in the R ² radical can be substituted by two or preferably one of the following radicals in the o-, m- or p-position: C ₁ -C ₄ -alkyl such as methyl, ethyl, n-propyl, iso-propyl, n-butyl iso-butyl, sec. butyl or tert.-butyl, - C ₁ -C ₃ haloalkyl such as chloromethyl, dichloromethyl, trichloromethyl or trifluoromethyl, - C ₁ -C ₄ alkoxy such as methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, iso-butoxy, sec.-butoxy, tert.-butoxy or

Methylenedioxy, - C ₁ -C ₃ haloalkoxy such as difluoromethoxy, trifluoromethoxy, chlorodifluoromethoxy, 1,1,2,2-tetrafluoroethoxy or

1,1,2-trifluoro-2-chloroethoxy, - C ₁ -C ₄ alkyl mercapto such as methyl mercapto, ethyl mercapto,

n-propylmercapto or n-butylmercapto, - C ₁ -C ₃ -halogeπalkylmercapto such as difluoromethylmercapto,

Trifluoromethylmercapto, chlorodifluoromethylmercapto or 1,1,2,2-tetrafluoroethylmercapto, - carboxy, advantageously as free acid, - sulfo, advantageously as free acid, - C ₁ -C ₄ alkylsulfonyl such as methylsulfony 1, ethylsulfonyl,

n-propylsulfonyl or n-butylsulfonyl, - C ₁ -C ₃ haloalkylsulfonyl such as chloromethylsulfonyl or

Trifluoromethylsulfonyl, - Nitro or - Halogen such as fluorine, chlorine or bromine. The following radicals are preferred for R ² : - straight-chain or branched C ₁ -C ₄ alkyl, in particular methyl, - unsubstituted phenyl, - by C ₁ -C ₄ alkyl, in particular phenyl substituted by methyl, - by C ₁ -C ₃ haloalkyl substituted phenyl - C ₁ -C ₄ alkoxy, in particular by methoxy substituted phenyl, - substituted with C ₁ -C ₃ haloalkoxy, phenyl, - by C ₁ -C ₃ -Halogenalkylmercapto substituted phenyl - C ₁ - C ₄ alkylsulfonyl, in particular phenyl substituted by methylsulfonyl, phenyl substituted by C ₁ -C ₃ haloalkylsulfonyl, phenyl substituted by nitro and phenyl substituted by halogen.

After the reaction has taken place, the compounds I obtained can be purified by the customary methods, for example by recrystallization or distillation, and / or, if desired, be made up by the customary methods, for example by granulation from the melt before or after a purification step. The process according to the invention makes it possible to produce 4H-3,1-benzoxazin-4-one I in a simple manner efficiently, ie with high yields, and economically cheap. You do not need any auxiliary chemicals such as solvents or catalysts. The implementation was practically complete in a short time, which is reflected in a high space-time yield. The product is usually obtained in a sufficiently pure form, since the reaction takes place without any significant side reactions, so that further cleaning operations are unnecessary for many applications.

The 4H-3,1-Benzoxazin-4-one I are important compounds for a wide range of applications, for example as pesticides, medicines, detergent additives or UV stabilizers. Thus, compounds I with halogen, methyl or methoxy for R ¹ and halophenyl, haloalkylphenyl, haloalkoxyphenyl, haloalkylmercaptophenyl or haloalkylsulfony iphenyl, each having 1 to 3 carbon atoms in the alkyl group for R ^{2, can be used} as selective herbicides. Certain 2-substituted 4H-3,1-benzoxazin-4-ones are suitable as cold bleach activators in detergents.

Example Preparation of 2-phenyl-4H-3,1-benzoxazin-4-one

163.1 g (1.0 mol) of isatoic anhydride and 154.7 g (1.1 mol) of benzoyl chloride were reacted with one another at a heating jacket temperature of the reaction vessel of 220 to 225 ° C., with stirring, whereby hydrogen chloride and carbon dioxide escaped. The internal temperature in the reaction mixture rose from 197 ° C. to 215 ° C. in the course of the reaction. The conversion depending on the reaction time could be determined from the amount of gas released by the reaction: Reaction time [h] conversion [%] 1 8

2 32

3 72

4 93

5 99

6 100

After the evolution of gas had ended after 6 hours, the crude product was purified by distillation at 160 ° C./1 mbar. 227 g of the title compound (corresponding to a yield of 94%) were obtained in the form of a colorless oil, which crystallized on cooling.

Claims

1 . Process for the preparation of 4H-3, 1-benzoxazin-4-ones of the general formula I in the

R ^{1 is} hydrogen, C ₁ -C ₄ alkyl, C ₁ -C ₄ alkoxy, carboxyl,

Denotes sulfo, nitro or halogen,

R2 C ₁ -C ₂₁ alkyl, phenyl or phenylalkyl with 1 to

4 C atoms in the alkyl group, where a phenyl nucleus is represented by one or two C ₁ -C ₄ alkyl groups, C ₁ -C ₃ haloalkyl groups, C ₁ -C ₄ alkoxy groups, C ₁ -C ₃ haloalkoxy groups, C ₁ -C ₄ alkyl mercapto groups, -C-C3-haloalkyl mercapto groups, carboxyl groups, sulfo groups, C ₁ -C ₄ alkylsulfonyl groups, C ₁ -C ₃ haloalkyl sulfonyl groups, nitro groups or halogen atoms, and n can be 1 or 2, by reaction of isatoic anhydrides of the general formula II

with acyl halides of the general formula III

where X denotes chlorine or bromine, characterized in that the reaction is carried out at an outside temperature of 215 to 280 ° C and the reactants II and III are allowed to react with one another at this temperature for at least 4 hours.

2. A process for the preparation of 4H-3,1-benzoxazin-4-ones I according to claim 1, characterized in that one carries out the reaction at an outside temperature of 220 to 250 ° C.

3. A process for the preparation of 4H-3,1-benzoxazin-4-ones I according to claim 1 or 2, characterized in that 1.0 to 1.5 mol of acyl halide III is used per mole of isatoic anhydride II.