Regeneration of onium fluoride-HF adducts

Details Regeneration of onium fluoride-HF adducts Regeneration of onium fluoride-HF adducts

2002-03-04

2003-02-18

Langel, Wayne A. (Department: 1754)

Chemistry of inorganic compounds

Halogen or compound thereof

Hydrogen halide

C423S486000, C423S507000, C502S028000, C502S036000, C570S163000, C570S164000, C570S165000, C570S170000

Reexamination Certificate

active

06521199

ABSTRACT:

BACKGROUND OF THE INVENTION
The invention relates to a method for regenerating spent ammonium fluoride-HF adducts. Adducts of ammonium fluorides and HF can be used as fluorination reagents. European patent application no. EP-A 901,999, for example, describes the production of sevoflurane from the corresponding fluorinated ether, using HF and an amine. The work-up is performed with the addition of water, with the result that the onium fluoride-HF adduct is destroyed.
U.S. Pat. No. 4,372,938 describes the production of SF
4
using ammonium fluoride adducts. The spent onium fluoride-HF adducts are regenerated by contacting with hydrogen fluoride and are reused in the production of SF
4
. The amines used are nitrogen-containing, heterocyclic aromatic compounds.
SUMMARY OF THE INVENTION
The object of the present invention is to provide an improved regeneration method.
It is also an object of the invention to provide a regenerated NH
3
or amine-HF adduct product.
These and other objects are achieved by providing an improved process for producing fluorine-containing compounds from chlorine-containing or bromine-containing compounds by chlorine-fluorine exchange or bromine-fluorine exchange using an onium fluorid-HF adduct as a reagent or catalyst, in which spent onium fluoride-HF adduct is regenerated using HF in the presence of a liquid carboxylic acid; or a spent trialklyammonium fluoride-HF adduct or a spent HF adduct of a cyclic saturated amine is regenerated using HF.
According to the inventive method for producing fluorine-containing compounds from chlorine-containing or bromine-containing compounds by chlorine-fluorine exchange or bromine-fluorine exchange using onium fluoride-HF adducts as reagent or catalyst, spent onium fluoride-HF adducts are regenerated continuously or batchwise using HF in the presence of a liquid carboxylic acid, and/or spent trialklyammonium fluoride-HF adducts or spent HF adducts of cyclic saturated amines are regenerated using HF.
As used herein, the term “spent” means that the ratio of amine to HF has become unacceptably high and/or the HCl or HBr content has become unacceptably high. In the regeneration, the content of HCl (or HBr) in particular is reduced to an acceptable level—for example, to less than 1 mole HCl per mole amine or NH
3
. In this respect, the HF content can be brought to the desired level by the addition, evaporation, or admixture of adducts with suitable concentrations.
It is advantageous to carry out the regeneration in an autoclave or pressurized vessel with the addition of HF at an elevated temperature ranging from 80 to 120° C., for example. The HCl or HBr that is liberated can be removed from the gas phase after the autoclave is opened. As an example, inert gas can be passed through the autoclave to remove the gas phase.
It has been shown to be advantageous if substantially all the HF for the fluorination is not consumed during the fluorination reaction. Although regeneration can be carried out even if the adduct has been essentially completely converted to ammonium chloride or onium chloride, or to the corresponding bromide, the regeneration is easier to perform when the ratio of amine to HF does not fall below 1 during the fluorination reaction.
Of course, the ratio of amine to hydrogen fluoride may be adjusted in the regenerated product. For many applications it is desirable for the ratio of amine to hydrogen fluoride in the adduct to lie between 1:1.1 and 1:3.5, preferably between 1:2 and 1:3. This can be achieved, for example, by removing the excess hydrogen fluoride in the regenerated product by heating or distillation.
According to U.S. Pat. No. 4,472,938, it is preferred to used ammonium fluoride-HF adducts based on nitrogen-containing aromatic compounds, such as pyridinium fluoride-HF adducts, in the production of sulfur tetrafluoride. In the regeneration method without addition of acid according to the present invention, an embodiment provides for the use of spent trialkylammonium fluoride-HF adducts or HF adducts of cyclic saturated amines. Such compounds are advantageously used in the regeneration method, in that it has been determined that spent trimethylammonium fluoride-HF or triethylammonium fluoride-HF adducts, and thus adducts of amines containing short alkyl chains, readily liberate HCl during regeneration. Spent trialkylammonium fluoride-HF adducts containing alkyl groups that have at least three carbon atoms are less prone to form solids. Naturally, this is an advantage for regeneration without the addition of acid. In addition, spent HF adducts of amines in which the nitrogen is contained in a saturated 5- or 6-member ring system and which also contain heteroatoms such as oxygen—adducts of piperidine or pyrrolidine, for example—can be regenerated in this manner.
When acid is not added, the regeneration of spent trimethylamine-HF adducts, triethylamine-HF adducts, tripropylamine-HF adducts, and tributylamin-HF adducts is especially preferred.
In accordance with one variant of the process of the invention, the spent adducts are regenerated by the addition of a liquid carboxylic acid (this term also includes dicarboxylic acids and tricarboxylic acids). Carboxylic acids, especially those containing a total of 2 to 4 carbon atoms, are preferably substituted by halogen atoms, in particular fluorine atoms. Trifluoroacetic acid is especially preferred as an additive.
Adducts containing short-chain alkyl groups have a tendency to form solids; this can be counteracted by using a liquid carboxylic acid, particularly trifluoroacetic acid. For spent adducts of amines containing long-chain alkyl groups, it is necessary to expel the contained HCl when the operation involves addition of a carboxylic acid. It is often sufficient to add up to 10 mol % of the acid, relative to the spent onium-HF adduct calculated as 100 mol %. Of course, even more acid may be added, up to 20 mol % or more, for example. 80 mol % is regarded as the upper limit, since side reactions may occur when more than 80 mol % acid is added.
According to a very particularly preferred embodiment, spent trialkylammonium fluoride-HF adducts, independent of the length of the alkyl groups on the nitrogen, are regenerated by adding a liquid carboxylic acid, preferably trifluoroacetic acid. The reduced tendency toward formation of solids and the easy expulsion of HCl gas are advantageous.
The method according to the invention with the addition of acid can generally be used to regenerate HF adducts of ammonia and amines. These amines may be primary, secondary, or tertiary amines. The substituents are preferably linear or branched alkyl groups containing 1 to 12 carbon atoms. Adducts of cyclic amines such as pyrrolidine, N-methylpyrrolidine, or piperidine may be used as well. In addition, amines with aromatic substituents such as aniline, or amines containing nitrogen in an aromatic ring system such as pyridine, may be regenerated. The regeneration method is particularly well suited for HF adducts of the aforementioned cyclic or aromatic amines as well as for secondary and tertiary amines, especially when these secondary and tertiary amines are substituted with 1 to 5, preferably 2 to 4 carbon atoms per substituent. Methyl, ethyl, n-propyl, i-propyl, n-butyl, and i-butyl are preferred substituents.
The method according to the invention allows the reuse of spent HF adducts of ammonia and amines from fluorination reactions. The regeneration method according to the invention may be used to regenerate spent adducts from the production of, for example, acid fluorides from acid chlorides, such as the production of carboxylic acid fluorides or sulfuryl fluoride from the corresponding chlorides. This applies also to spent adducts originating from the production of fluoroalkyl groups from chloroalkyl groups. Examples of such reactions include the production of fluoro(hydro)carbons, fluorochloro(hydro)carbons, and the analogous bromine derivatives from the corresponding chlorine compounds obtained by fluorine-chlorine exchange or fluorine-bromine exchange. Another exam

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