Process for separating hydrogen chloride from a mixture...

Details Process for separating hydrogen chloride from a mixture... Process for separating hydrogen chloride from a mixture...

2001-06-27

2003-02-18

Manoharan, Virginia (Department: 1764)

Distillation: processes, separatory

Vaporization zone under positive pressure or vacuum

Including the addition of water or steam

C203S094000, C203S096000, C203S097000, C203S098000, C423S488000, C548S555000

Reexamination Certificate

active

06521097

ABSTRACT:

FIELD OF THE INVENTION
The present invention relates to a process for separating hydrogen chloride from a mixture comprising an N-alkyl-2-pyrrolidone and hydrogen chloride by means of distillation.
BACKGROUND OF THE INVENTION
N-Alkylpyrrolidone containing hydrogen chloride is formed in the preparation of isochroman-3-ones by the process described in EP 0 949 256. When N-methyl-2-pyrrolidone is used, an N-methyl-2-pyrrolidone containing hydrogen chloride is obtained. After hydrogen chloride has been separated off, the N-methyl-2-pyrrolidone can be reused in the process. The reuse of the N-methyl-2-pyrrolidone is advantageous both from an economic point of view and in terms of ecologocial aspects. Reuse avoids undesirable waste products which would have to be disposed of.
U.S. Pat. No. 3,651,166 concerns a process for recovering hydrogen halide and organic bases, for example N-methyl-2-pyrrolidone, by heating their salts to dissociation temperature. Example II describes the recovery of anhydrous HCl from an N-methyl-2-pyrrolidone (NMP) solution containing water and HCl by distillation. Here, the water is firstly distilled off until the temperature has reached about 120° C. Residual water and a small proportion of the NMP is then distilled off at 150° C. Anhydrous HCl is subsequently separated off at from 175 to 180° C.
Although anhydrous HCl is obtained in this way, this HCl is contaminated with N-methylpyrrolidone to a not inconsiderable extent and cannot be directly processed further. Rather, this contaminated HCl either has to be purified in a separate, costly process or has to be disposed of. Furthermore, entrained solids (sublimates) can deposit at the top of the distillation column and in the downstream lines and lead to blockages. See also Comparative Example 2A.
SUMMARY OF THE INVENTION
There is therefore a need for a process which avoids the abovementioned disadvantages, can be implemented in a simple manner, gives pure hydrogen chloride and makes possible a satisfactory separation of hydrogen chloride from the N-alkyl-2-pyrrolidone.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
This object is achieved by a process for separating hydrogen chloride from a mixture comprising an N-(C
1
-C
18
)-alkyl-2-pyrrolidone and hydrogen chloride, which comprises distilling the mixture comprising an N-(C
1
-C
18
)-alkyl-2-pyrrolidone and hydrogen chloride at from 100 to 220° C. and from 50 to 850 hPa in the presence of water by means of a distillation column, condensing the water as water-hydrogen chloride azeotrope at the top by cooling, returning the water-hydrogen chloride azeotrope to the distillation column, separating off gaseous hydrogen chloride at the top and taking off the N-(C
1
-C
18
)-alkyl-2-pyrrolidone from the bottom.
The process of the invention surprisingly gives both a pure hydrogen chloride which can, for example, be absorbed in water and used further as a water-containing hydrogen chloride and an N-alkyl-2-pyrrolidone which is very largely free of hydrogen chloride and can likewise be reused without additional work-up, for example in the preparation of isochroman-3-ones.
The process of the invention has the advantage that it can be implemented in simple ways without requiring any great engineering outlay.
For the purposes of the present invention, N-alkyl-2-pyrrolidones are compounds of the formula
where R is a straight-chain or branched C
1
-C
18
-alkyl radical.
The N-alkyl-2-pyrrolidones form relatively stable adducts with hydrogen chloride, but these can be dissociated at an elevated temperature (dissociation temperature) into hydrogen chloride and the N-alkyl-2-pyrrolidone. The N-alkyl-2-pyrrolidone-hydrogen chloride adducts tend to form sublimates. This is particularly true of the N-methyl-2-pyrrolidone-HCl adduct, which sublimes relatively easily.
A further advantage of the process of the invention is that the deposition of solids and sublimates which cause blockages in the lines leading from the top of the distillation column is, surprisingly, effectively suppressed.
The mixture comprising the N-alkyl-2-pyrrolidone and HCl can be placed in the bottom of the distillation column and heated (a batchwise procedure). However, it is also possible to feed the mixture comprising the N-alkyl-2-pyrrolidone and HCl in gaseous or liquid form into the distillation column and to carry out the process of the invention continuously. A predetermined amount of water is added to ensure that the distillation proceeds in the presence of water and a water-hydrogen chloride azeotrope can be formed at the top of the distillation column. If the process is carried out continuously, it is advisable to introduce the mixture comprising N-alkyl-2-pyrrolidone and HCl into the lower half, in particular the lower third, of the distillation column and to take off the N-alkyl-2-pyrrolidone which has been very largely freed of HCl at the bottom at a rate corresponding to that at which the mixture is fed into the column.
Pressure and temperature are set so that the mixture comprising hydrogen chloride and the N-alkyl-2-pyrrolidone boils. The process is particularly advantageous when the temperature selected is above the sublimation temperature of the N-alkyl-2-pyrrolidone-HCl adduct. The sublimation temperature of this N-alkyl-2-pyrrolidone-HCl adduct is above the dissociation temperature of the adduct, i.e. above the temperature at which the adduct decomposes into HCl and the N-alkylpyrrolidone.
At the top of the distillation column, a gaseous mixture of water and hydrogen chloride which can still contain small amounts of N-alkyl-2-pyrrolidone is obtained. The water is condensed at the top of the column and is thus obtained as the water-hydrogen chloride azeotrope which may still contain minor amounts of N-alkyl-2-pyrrolidone. At the same time, excess gaseous hydrogen chloride is present at the top of the distillation column. This hydrogen chloride is not condensed together with the water as hydrogen chloride-water azeotrope, but leaves the column at the top as pure hydrogen chloride in gaseous form. Any entrained N-alkyl-2-pyrrolidone or organic product separates out in liquid form. However, the amounts concerned are generally very small.
The water-hydrogen chloride azeotrope condensed at the top by cooling is returned to the distillation column. The water vaporizes again and once more condenses at the top of the distillation column as water-hydrogen chloride azeotrope and is again returned to the distillation column. In this way, the water is circulated.
Since minor amounts of water in the form of water vapor also escape together with the excess gaseous hydrogen chloride which is discharged at the top, it may become necessary to add appropriate amounts of water to the distillation during prolonged operation so as to maintain the formation of the water-hydrogen chloride azeotrope and its return to the distillation to the desired extent.
Should the feed mixture comprising N-alkyl-2-pyrrolidone and hydrogen chloride contain water, it may become necessary during prolonged operation of the distillation, in particular in the case of continuous distillation, to discharge water in the form of the water-hydrogen chloride azeotrope at the top of the column so as to prevent the amount of water from rising in an uncontrolled manner, but instead to limit the proportion of water to the amount required for the distillation.
Good results can be obtained when using a mixture comprising N-(C
1
-C
12
)-alkyl-2-pyrrolidone and hydrogen chloride, in particular N-(C
1
-C
8
)-alkyl-2-pyrrolidone and hydrogen chloride, preferably N-(C
1
-C
4
)-alkyl-2-pyrrolidone and hydrogen chloride, particularly preferably N-methyl-2-pyrrolidone and hydrogen chloride.
As mentioned at the outset, the distillation is carried out at a temperature of from 100 to 220° C., in particular from 120 to 200° C., preferably from 130 to 180° C.
The addition of an organic solvent is not necessary, i.e. the distillation is carried out in the absence of an organic solvent.
As mentioned above, the distillation is carried out at a pressure of from

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