Process for preparing pyrrolidone derivative

Details Process for preparing pyrrolidone derivative Process for preparing pyrrolidone derivative

1999-11-23

2002-08-06

Chang, Ceila (Department: 1626)

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

Organic compounds

Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

active

06429316

ABSTRACT:

FIELD OF THE INVENTION
This invention relates to a process for preparing a pyrrolidone derivative. More particularly, it relates to an improvement in the process of preparing an N-alkyl-2-pyrrolidone comprising the reaction between &ggr;-butyrolactone, etc. and alkylamines.
Pyrrolidone derivatives are used as heat-resistant solvents in various industrial processes, for example, as a metal cleaner or a solvent for functional polymers, and have recently been increasing the demand.
BACKGROUND OF THE INVENTION
Pyrrolidone derivatives, such as an N-alkyl-2-pyrrolidone, are generally prepared on an industrial scale by the reaction between a monoalkylamine and &ggr;-butyrolactone. The starting monoalkylamine is industrially prepared by isolation from a mixture of a trialkylamine, a dialkylamine, and a monoalkylamine which is obtained by dehydration reaction between a corresponding alkanol and ammonia.
Use of the mixture of a trialkylamine, a dialkylamine, and a monoalkylamine as a starting material instead of a monoalkylamine is also proposed as disclosed in JP-B-
47-18751.
According to this technique, however, the amounts of the alkylamines and &ggr;-butyrolactone added do not satisfy formula:
1.0≦(
A
1
+
A
2
/2.5)/(
B
1
+
B
2
+
B
3
)
wherein A
1
, A
2
, B
1
, B
2
, and B
3
represent the molar amounts of a primary amine, a secondary amine, &ggr;-butyrolactone, 4-hydroxybutyric acid, and low-molecular 4-hydroxybutyric acid polymers, respectively. Further, the yield and reaction rate achieved are lower than in starting with a monoalkylamine alone.
JP-B-6-78305 proposes a process in which monomethylamine is used in excess, and a mixture of the monoalkylamine, a trialkylamine, a dialkylamine, and ammonia resulting from isomerization of the unreacted monomethylamine during the reaction is recovered and recycled to the reaction system, which is replenished with fresh monomethylamine. In this process, however, the monomethylamine content in the alkylamine apparently exceeds 85% by weight, which is industrially unfavorable as compared with the process using a mixed amine.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide a process for preparing a pyrrolidone derivative easily and in high yield by using, as one of starting materials, a primary, secondary or tertiary amine or a mixture thereof, particularly the mixed amine obtained in alkylamine production from ammonia and an alkanol.
As a result of extensive investigations, the present inventors have found that &ggr;-butyrolactone reacts with a mixed alkylamine in a specific ratio to give a pyrrolidone derivative in as high a yield (e.g., 90% or more) as in using a monoalkylamine.
The gist of the invention lies in a process for preparing a pyrrolidone derivative which comprises allowing at least one of &ggr;-butyrolactone, 4-hydroxybutyric acid, and a low-molecular polymer of 4-hydroxybutyric acid to react with an alkylamine, wherein (i) the content of a primary amine in the alkylamine is 85% by weight or lower, and (ii) the molar ratio of the total amount of the charged primary and secondary amines to the total amount of the charged &ggr;-butyrolactone, 4-hydroxybutyric acid, and low-molecular 4-hydroxybutyric acid polymers satisfies formula:
1.0≦(
A
1
+
A
2
/2.5) (
B
1
+
B
2
+
B
3
)
wherein A
1
, A
2
, B
1
, B
2
, and B
3
represent the molar amounts of a primary amine, a secondary amine, &ggr;-butyrolactone, 4-hydroxybutyric acid, and low-molecular 4-hydroxybutyric acid polymers, respectively.
PREFERRED EMBODIMENTS OF THE INVENTION
One of the starting materials used in the process of the invention is selected from &ggr;-butyrolactone, 4-hydroxybutyric acid, and a low-molecular polymer of
4
-hydroxybutyric acid. The term “low-molecular” as used in the specification and claims is intended to mean “to have a degree of polymerization of about 2 to 10”. These starting materials can be used either individually or as a mixture thereof. A mixture resulting from an equilibrium reaction in the presence of water is also employable.
The alkylamine, the other starting material used in the invention, can be a mixture of at least two of a primary amine, a secondary amine and a tertiary amine, or a primary or secondary amine could be used alone.
The alkyl moiety in the alkylamines maybe cyclic or acyclic, either straight or branched, and may be saturated or unsaturated. The alkyl moieties in a secondary or tertiary amine may be either the same or different. It is preferred that the alkyl moiety be a saturated and straight-chain alkyl group and that the two or three alkyl groups in a secondary or tertiary amine be the same. While not limiting, the number of the carbon atoms in the alkyl group is preferably 1 to 20, still preferably 1 to 10, and particularly preferably 1 to 3.
Examples of the primary amines are methylamine, ethylamine, and propylamine; the secondary amines are dimethylamine, diethylamine, dipropylamine, methylethylamine, methylpropylamine, and ethylpropylamine; and the tertiary amines are trimethylamine, triethylamine, tripropylamine, dimethylethylamine, dimethylpropylamine, diethylmethylamine, diethylpropylamine, dipropylmethylamine, and dipropylethylamine. Preferred of them are methylamine as a primary amine, dimethylamine as a secondary amine, and trimethylamine as a tertiary amine.
Where mixed amines are used, the mixing ratio can be the ratio of mixed amines that are generally obtained in industry, i.e., 20 to 40% by weight of a primary amine, 50 to 75% by weight of a secondary amine, and 5 to 10% by weight of a tertiary amine, although the mixing ratio is not limited thereto. For the economical standpoint, to use mixed amines having the mixing ratio in the above range is more advantageous than to use a primary, secondary or tertiary amine alone. From the standpoint of reaction rate, however, a primary amine is preferred to a tertiary amine. Taking these points into consideration, it is desirable that the primary amine content in the starting alkylamine be 85% by weight or lower, preferably 20% to 85% by weight, more preferably 40% to 85% by weight.
It is required for obtaining pyrrolidone derivatives in high yield that the alkylamine be used in such an amount that the molar ratio of the total amount of the primary and secondary amines to the total amount of the &ggr;-butyrolactone, 4-hydroxybutyric acid, and low-molecular 4-hydroxybutyric acid polymers, which ratio is represented by formula:
(
A
1
+
A
2
/2.5)/(
B
1
+
B
2
+
B
3
)≦10
wherein A
1
, A
2
, B
1
, B
2
, and B
3
represent the charged amount (mole number) of a primary amine, a secondary amine, &ggr;-butyrolactone, 4-hydroxybutyric acid, and low-molecular 4-hydroxybutyric acid polymers, respectively, and will be referred to as “parameter value”, be 1.0 or greater. If the starting compounds are used in amounts giving the parameter value of smaller than 1.0, disadvantages can result, such as reduction in conversion of &ggr;-butyrolactone or reduction in selectivity to the desired pyrrolidone derivative.
While not limiting, the upper limit of the parameter value is usually 10.0, preferably 5.0. With the parameter value below this, an excessive load can be avoided in the step of recovering and recycling the alkylamine.
The reaction is preferably carried out in the presence of water. Water is usually used in an amount of 0.5 to 20 mol, preferably 2 to 10 mol, still preferably 3 to 5 mol, per mole of the total amount of &ggr;-butyrolactone, 4-hydroxybutyric acid, and low-molecular 4-hydroxybutyric acid polymers. With the amount of water being in an appropriate range, the reaction rate increases, and the reverse reaction from the produced pyrrolidone derivative to the starting &ggr;-butyrolactone can be suppressed.
The reaction temperature is usually in the range of from 190° to 350° C. From the viewpoint of purity, tone, etc. of the product, the reaction temperature is preferably from 220 to 350° C., still preferably from 230 to 300° C., particularly preferably from 235 to 275° C.
The reaction pres

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