Heterocyclic aromatic compounds thiophene

Cyclic compounds that contain at least one atom other than carbon within their ring are called heterocyclic compounds, and those that possess aromatic stability are called het erocyclic aromatic compounds Some representative heterocyclic aromatic compounds are pyridine pyrrole furan and thiophene The structures and the lUPAC numbering system used m naming their derivatives are shown In their stability and chemical behav lor all these compounds resemble benzene more than they resemble alkenes... 

Section 12 18 Heterocyclic aromatic compounds may be more reactive or less reactive than benzene Pyridine is much less reactive than benzene but pyrrole furan and thiophene are more reactive... 

Since thiophene derivatives, heterocyclic aromatic compounds, are sensitive toward electrophilic substitution reactions, the bromination of these compounds generally gives a mixture of mono-, di-, and other poly-substituted bromination products (ref. 19). However, we have recently found that BTMA Br3 is a useful... 

Friedel-Crafts reaction of phosgene with heterocyclic aromatic compounds is also difficult to stop at the acid chloride stage. However, under selected conditions, heteroaromatics such as thiophene can be directly acylated to give thiophenecarbonyl chloride [Scheme T9] (Ref. 15) ... 

Furan, thiophene, pyrrole, and pyridine are all examples of heterocyclic aromatic compounds (heteroaromatic compounds). The heteroatoms in some of these compounds (furan, thiophene, pyrrole) contribute one lone pair to the aromatic system, whereas in others (pyridine) they contribute none. You can determine how many lone pairs a heteroatom contributes to the aromatic system by examining the effect of lone-pair donation on the hybridization of the heteroatom. For example, if the N atom of pyridine used its lone pair to participate in resonance, it would have to be sp-hybridized (one p orbital required for the N=C n bond, one for the lone pair used in resonance), but sp hybridization requires 180° bond angles, which are not possible in this compound. Therefore the N atom must be sp2-hybridized, and the N lone pair must be in a hybrid orbital that is orthogonal to the cyclic array of p orbitals. In pyrrole, by contrast, if the N atom uses its lone pair in resonance, the N atom must be sp2-hybridized, which is reasonable. Therefore, there is a cyclic array of p orbitals in pyrrole occupied by six electrons (two from each of the C=C it bonds and two from the N lone pair), and pyrrole is aromatic. 

The chemical reactivity of simple heterocyclic aromatic compounds varies widely in electrophilic substitution reactions, thiophene is similar to benzene and pyridine is less reactive than benzene, while furan and pyrrole are susceptible to polymerization reactions conversely, pyridine is more readily susceptible than benzene to attack by nucleophilic reagents. These differences are to a considerable extent reflected in the susceptibility of these compounds and their benzo analogues to microbial degradation. In contrast to the almost universal dioxygenation reaction used for the bacterial degradation of aromatic hydrocarbons, two broad mechanisms operate for heterocyclic aromatic compounds ... 

Cycloaddition to five-membered heterocyclic aromatic compounds is well documented. Examples reported this year include the formation of azetidine adducts (67) by irradiation of 3-(p-cyanophenyl)-2-isoxazoline with furan or thiophen (and also with benzene) benzophenone-sensitized reaction of selenophen with dimethylmaleic anhydride (68) to give 1 1 and 1 2 adducts and oxetan formation from benzophenone and 1-acylimidazoles (69), thiazoles, or isoxazoles. ... 

More and more, solid catalysts like zeolites, clays or resins are used instead of traditional catalysts. Thus, zeolites are good catalysts for the acylation of non-heterocyclic aromatic compounds, both in the gas phase [2] and in the liquid phase [3]. The acylation of thiophene and of furan can also be carried out in the gas phase with M-5 catalysts [4]. Lasdo and co-woikers have shown that modified clays like montmorillonite doped with ZnCl2 can catalyse the reactioi of arenes with substituted benzoyle chlorides in good yields [5] (70 to 100%). Delmas and co-workers have reported the acylation of furan by carboxylic acids with nafion-H [6] (sulfonic resin) and duolite [7] (ion exchanged phosphonic resin). One of the advantages of these catalysts is the safety of environment. Actually, the use of homogeneous catalysts causes problems of corrosion, waste and troublesome workups [8,9]. 

Heterocyclic aromatic compounds contain C and H atoms other than carbon and hydrogen (Fig. 6). For the monocyclic molecules Hiickel s rule is applicable. For example both pyridine and pyrrole contain six ti electrons. Unlike the former the lone pair of the latter is delocalized. Armit and Robinson have shown a connection between the electronic sextet and the heteroaromaticity. Due to the electronegativity difference between carbon and nitrogen the bonds in pyridine are not of equal length and the delocalization is not perfect. Five membered heteroaromatics with oxygen and sulfur are furan and thiophene respectively. Pyrazole/imidazole, triazoles and tetrazoles are five membered heteroaromatics with two, three and four nitrogen atoms respectively. Three important aromatic six membered heterocyclic molecules are pyrimidine, pyrazine and pyridazine. Benzofused... 

Pyrrole, fiiran, and thiophene are heterocyclic aromatic compounds that undergo electrophilic aromatic substitution reactions preferentially at C-2. They are more reactive than benzene toward electrophilic aromatic substitution. 

As an aromatic compound, thiophene is stabilised by resonance energy - actual values for the stabilisations of five-membered aromatic heterocycles (Fig. 2 kJ mol ) vary according to the assumptions made, but are always in the same relative order benzene (150), thiophene (122), pyrrole, (90), and furan (68) -thiophene is the most aromatic of the five-membered heterocyclic trio, i.e. it is the least like a diene. In its reactions, too, thiophene behaves very much like a carbocyclic aromatic compound, exceptions being associated with the presence of the heteroatom. 

In many ways, the electron-rich five-membered aromatic heterocycles behave very much like carbocyclic aromatic compounds when it comes to lithiation. Lithiation a to O or S of furan and thiophene is straightforward (Scheme 130) . The usual selection of orf/io-directing groups allows lithiation at other positions and some examples... 

Heterocyclic aromatics in fuel such as pyridine, indole and condensed thiophene compounds are known to darken fuel color. They have also been shown to lead to an increase in the deposit forming tendencies of fuel. Aromatic peroxides can also react to form higher-molecular-weight, sludgelike material in fuel. 

Methyl-substituted thiophenes are also capable of reaction with benzalaniline, provided that the 5-position carries a carbo- or heterocyclic aromatic group, as, for example, 2-(benzoxazol-2-yl)-5-methyl-thiophene (109), which yields the styryl derivative 110.11 The isomeric compound 111 may be obtained analogously from 2-(/ -tolyl)benzox-azole and Schiff s base from 2-formylthiophene and p-chloroaniline. 

Leonid Belen kii was born in Moscow, and he graduated from M. V. Lomonosov Moscow State University in 1953 with Professor A. P. Terentiev as supervisor in organic chemistry. Since 1955, he has worked as junior, senior (since 1966), and leading scientist (since 1988) at N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, where he obtained his Ph.D. degree (1963) under the direction of Professor Ya. L. Gol dfarb and his Degree of Dr. Chem. Sci. (1974) and rank of Professor in Chemistry (1991). His scientific interests include all aspects of chemistry of heterocyclic and aromatic compounds, particularly electrophilic substitution in benzene, thiophene, furan, and azole series as well as organosulfur chemistry. 

Thiophene is an aromatic compound. Its structure can be assumed to be derived from benzene by replacement of two annular CH groups with sulfur. The sulfur atom in this five-membered ring acts as an electron-donating heteroatom by contributing two electrons to the aromatic sextet and thiophene is thus considered to be an electron-rich heterocycle. 

This may imply that the intermolecular coupling of various aryl halides with other heteroaromatic compounds may proceed. Indeed, it is now known that not only the special heteroaromatic halides but also usual aryl halides can react with a variety of five-membered aromatic heterocycles, including furans, thiophenes, and azole compounds such as M-substituted imidazoles, oxazoles, and thiazoles [133-137]. The arylation of azoles can be carried out using iodobenzoate immobilized on an insoluble polymer support [138]. Related intermolecular reactions of indole [139] and imidazole [140] derivatives have also been reported. 

The anodic methoxylation of aromatic compounds such as naphthalene [41], anthracene [42], alkylbenzenes [31,43], phenols [44-46], anisoles [33,47-54] and other alkoxyben-zenes [53], methoxynaphthalenes [33], methoxyanthracenes [50,54], inden-l-ones [55], / a/r/-substituted anilides [56] and heterocyclic compounds, such as furans [57], thiophenes [58], and pyrroles [59], has received considerable attention. 

After a brief survey of the history of valence-bond isomers of aromatic compounds, new syntheses and the reactions of these isomers reported in the last decade are reviewed. In the second chapter, the valence-bond isomers of homoaromatic compounds, especially benzene derivatives, are described and in the third chapter those of heterocyclic compounds. Photoreactions of perfluoroalkylated aromatic compounds afford valence-bond isomers in high yields. These isomers are very stable and useful for the synthesis of highly strained compounds. Therefore, the emphasis is put on the chemistry of trifluoromethylated benzvalenes, Dewar thiophenes, and Dewar pyrroles. 

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