Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2002-03-20
2004-09-21
Lambkin, Deborah C. (Department: 1626)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
active
06794521
ABSTRACT:
FIELD OF THE INVENTION
The present invention relates to an ecofriendly process for the preparation 2-nitrothiophenes selectively from thiophene, using metal exchanged clay catalysts and nitric acid, dispensing with the use of acetic anhydride.
BACKGROUND OF THE INVENTION
Nitroheterocyclic compounds are important intermediates for drugs, pharmaceuticals and dyes. The chemistry of nitro-derivatives of many heterocyclic systems has long been established, but their commercial exploitation has developed only over the last 40 years. Synthetic nitrothiozoles like 2-acetylamino-5-nitrothiazole have antitrichomonal activity. In the 1940s, they were used for the treatment of war wounds. In 1947, the same drugs were found to be effective in the prevention of coccidiosis in chickens and enteritis in swine. These and other veterinary applications led to large volume usage in animal feed supplements. Thiophenes are used as chemotherapeutic agents although nifurzide obtained by condensation of 5-nitrothiophene-2-carboxylic acid hydrazide with 3-(2-nitro-5-furyl) acrolein contains both a nitrofuran and a nitrothiophene residue. Thiophene and its derivatives found applications in the pharmaceutical area over a wide range of drug types such as nonsteroidal, antiinflammatory, Rheumatoid and Osteoarthritis drugs, hypertension and heart drugs, antibiotics, antiglaucoma drug, veterinary products, agrochemical products and dyestuffs.
In the conventional nitration process, heterocyclic compounds such as furan, thiophene and pyrrole are nitrated by nitric acid and acetic anhydride.
Reference is made to Babasinian et al, Org. Syn. Coll., Vol.2, 466, 1943, wherein the nitration of thiophene is carried by reacting thiophene (0.63 mol) with fuming nitric acid (0.76 mol) in acetic anhydride-acetic acid solution at +10° C. to yield 85% of nitrothiophenes. Recrystallisation from hexane-isopropyl ether gave a nitrated product with the composition containing 85% of 2-nitrothiophene and 15% of 3-nitrothiophene. It is difficult to achieve the selectivity towards 2-nitrothiophene in the nitration of thiophene. The strongly electrophilic nitronium ion leads to significant yields of 3-isomer (12-15%). A preferred procedure is the slow addition of thiophene to an anhydrous mixture of nitric acid, acetic acid and acetic anhydride. The drawbacks are the use of expensive acetic anhydride, which is uneconomical and also exothermic and explosive nature of the reaction of acetic anhydride and nitric acid. Another draw back is the requirement for tedious separation of 2-nitrothiophene from 3-nitrothiophene in a low selective and high yield reaction.
Reference is made to Steinkopf, Ann., 545, 38, 1940 wherein the presence of 3-nitro-thiophene in the mononitration product from thiophene has been established. However, there has been no description of a procedure for obtaining the pure 2-nitrothiophene from the crude nitration product and for establishing the homogeneity of the 2-nitrothiophene.
Reference is made to Ostman et al,
Acta. Chem. Scand.,
22, 1687, 1968 wherein to separate the mixture of 2-nitrothiophene and 3-nitrothiophene in its components, the isomers have instead been obtained through the selective chlorosulfonation of the 3-nitrothiophene which is possible due to the slow reactivity of 2-nitrothiophene over 3-nitrothiophene. The isomeric mixture of nitrothiophene obtained from nitration of thiophene was chlorosulfonated with chlorosulfonic acid at 40° C. and the course of the reaction was followed by NMR. The successful protocol for high isomeric purity 2-nitrothiophene (99%) from the 2- and 3-nitrothiphene mixture is as follows. Nitrothiophene (85:15) was dissolved in ethanol free from chloroform and transferred to a four-necked flask carrying a stirrer, refluxing condenser, dropping funnel and a thermometer. While keeping the flask at 40° C., chlorosulfonic acid was added over a period of 5 min. A sample of reaction mixture was withdrawn and used in order to follow the reaction by GC or NMR. When 3-nitrothiophene was consumed, the reaction mixture was poured into ice water. The chloroform layer was separated and the water phase was extracted with chloroform. The combined chloroform solutions were washed with water and then shaken with aluminium oxide. The solution was finally dried over sodium sulfate and the solvent was removed with a rotary evaporator. The residue was then recrystallised from hexane-isopropyl ether to get 99% pure 2-nitrothiophene. The drawback is the requirement of tedious separation of 2-nitrothiophene from 3-nitrothiophene.
Reference is made to Steinkopf et al,
Ann,
501, 174, 1933 wherein 3-Nitrothiophene has higher melting point and is less soluble than the 2-nitro derivative and it can be purified easily by crystallization from ethanol.
Reference is made to Blatt et al,
J.Org.Chem.,
22, 1693, 1957, wherein nitration of thiophene with nitric acid in the absence of acetic anhydride gave a mixture of products, viz., 2-nitrothiophene, 2,5-dinitrothiophene and 2,4-dinitrothiophene. The drawback is poor product selectivity making the separation process difficult.
Attempts to circumvent acetyl nitrate processes are reported to be both difficult and dangerous.
Reference is made to Levitt et al,
Anal. Chem.,
25,196, 1953 wherein the action of nitric acid on thiophene results in the oxidative decomposition of the thiophene molecule, with apparently a quantitative conversion of the sulfur to sulfuric acid. The drawback is oxidative decomposition of the thiophene.
Reference is made to Levitt et al,
J.Am.Chem.Soc.,
76, 1951, 1954 wherein they studied the nature of intermediate products and by-products of this interesting reaction. The products formed by the action of 8N nitric acid on thiophene in cyclohexane are 2-nitrothiophene, 2,5-dinitrothiophene, maleic acid, oxalic acid and sulfuric acid. The drawback is poor product selectivity to encumber difficult separation.
Reference is made to Smith et al,
J.Org.Chem,
63, 8448, 1998 wherein thiophene is nitrated in excellent yields with regioselectivity under mild conditions using beta zeolite as a catalyst and a stoichiometric quantity of nitric acid and acetic anhydride. Thiophene gives a crude product that appeared to contain about 56% of the 3-nitro isomer and 44% of the 2-nitro isomer in an overall yield of about 80%. The drawbacks are the use of expensive acetic anhydride which is uneconomical and also exothermic and explosive nature of the reaction of acetic anhydride and nitric acid. Another draw back is the tedious separation of the 2-nitrothiophene from 3-nitrothiophene in a low selective and high yield reaction.
OBJECTS OF THE INVENTION
Accordingly, it is an object of the invention to provide a novel and ecofriendly process for the manufacture of 2-nitrothiophene dispensing with the use of acetic anhydride.
It is another object of the invention to provide a process for the manufacture of 2-nitrothiophene with >50% selectivity and good yield.
It is a further object of the invention to provide a process for the manufacture of 2-nitrothiophene which is carried out in a single step and is simple.
It is another object of the invention to provide a catalytic process for the manufacture of 2-nitrothiophene wherein the catalyst can be reused with consistent activity.
It is a further object of the invention to provide a process for the manufacture of 2-nitrothiophene which is clean, inexpensive and environmentally safe.
SUMMARY OF THE INVENTION
The above and other objects of the invention are achieved by preparing 2-nitrothiophene from thiophene with >50% selectivity, using solid acid catalysts.
Accordingly the present invention provides a process for the preparation of 2-nitrothiophene comprising nitrating thiophene using nitric acid in the presence of a solid acid catalyst selected from a montmorillonite clay catalyst and metal ion exchanged K10 montmorillonite clay catalyst, recovering nitrothiophene by concentration of the reaction mixture after separation of the catalyst.
In one embodiment of the invention, the nitration
Choudary Boyapati Manoranjan
Kantam Mannepalli Lakshmi
Ramprasad Kompella Vishweshwar
Ranganath Kalluri Venkata Sri
Council of Scientific and Industrial Research
Lambkin Deborah C.
Morgan & Finnegan , LLP
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