Acyl halides Friedel-Crafts reaction

Reaction XX. (6) Action of certain Anhydrous Metallic Halides (Aluminium Chloride, Aluminium Bromide, Aluminium and Hydrogen Chloride, Ferric Chloride) on a mixture of an Aromatic Hydrocarbon or certain Derivatives, and an Acyl Halide. (Friedel-Crafts.) (A. Ch., [6], 1, 518.)—This is an even more important application of the Friedel-Crafts synthesis than the methods of synthesising hydrocarbons (pp. 58, 60). The reactions involved are more readily controlled since the products, in presence of aluminium chloride, do not undergo further condensations. Usually these products have also the advantage of being more easily separated, for, as shown below in (iii.), the formation of isomers can be avoided. 

Another version of the Friedel-Crafts reaction uses acyl halides instead of alkyl halides and yields aryl ketones... 

Vinylic halides and aryl halides do not form carbocations under conditions of the Friedel-Crafts reaction and so cannot be used in place of an alkyl halide or an acyl halide... 

Alkenes can be acylated with an acyl halide and a Lewis acid catalyst in what is essentially a Friedel-Crafts reaction at an aliphatic carbon. ° The product can arise by two paths. The initial attack is by the acyl cation RCO (or by the acyl halide free or complexed see 11-14) at the double bond to give a carbocation ... 

Friedeb Crafts reaction Anisole undergoes Friedel-Crafts reaction, i.e., the all rl and acyl groups are introduced at ortho and para positions by reaction with alkyl halide and acyl halide in the presence of anhydrous alurntnlurn chloride (a Lewis acid) as catalyst. 

Aromatic compounds are usually readily alkylated or acylated by a Friedel-Crafts reaction.150 The combination of reagents used most commonly for aromatic alkylation is an alkyl halide with a strong Lewis acid (Equation 7.65). However, alkenes, alcohols, mercaptans, and a number of other types of organic... 

By this strategy, reactive carbon electrophiles can be generated for successful reaction with a variety of weak carbon nucleophiles. More important examples include the Friedel-Crafts reaction in which aromatic compounds (nucleophiles) react with alkyl and acyl halides (electrophiles in the presence of Lewis acids). 

The Friedel-Crafts reaction is polar (ionic) alkylation or acylation of electron-rich aromatics by alkyl cation or acyl cation species, derived from the reactions of alkyl halides or acyl halides with A1C13. Therefore, electron-rich aromatics such as anisole are very reactive, but electron-deficient aromatics such as pyridine are inert. 

At oxidation level 3, acid chlorides occupy a key position, since they may serve as a nearly universal substrate for an isohypsic transformation into any kind of carboxylic acid derivative. Acid halides are electrophiles that are synthetically equivalent to acyl cations (RCO ). In this capacity they are used for the synthesis of such important compounds as esters, amides (and hence, nitriles), thioesters, etc. (see Scheme 2.57), and for the formation of C-C bonds in the Friedel-Crafts reaction (see above). Acid chlorides may readily lose HCl upon treatment with triethylamine. This isohypsic conversion leads to ketenes, important reagents widely employed in [2 + 2] cycloadditions, as we will see later. 

Electrophiles for aromatic substitution include the halonium ion, the nitronium ion and the carbonium ion. The latter may be generated from alkyl and acyl halides using Lewis acid catalysis in the Friedel-Crafts reactions. 

One of the most important modifications of the Friedel-Crafts reaction involves the use of acid chlorides rather than alkyl halides. An acyl group, RCO—, becomes attached to the aromatic ring, thus forming a ketone the process is called acylation. As usual for the Friedel-Crafts reaction (Sec. 12.8), the aromatic ring undergoing substitution must be at least as reactive as that of a halobenzene catalysis by aluminum chloride or another Lewis acid is required. 

The course of the Friedel-Crafts reaction of alkenes is commonly considered to proceed by reaction of the alkene with the reactive acylating agent to form the 3-ketocarbenium ion, which can then either react with a nucleophile (usually halide) to give overall addition to the double bond, or eliminate a proton, forming unsaturated products (Scheme 1). 

This alternative to the Friedel-Crafts reaction, extensively developed by Stille and coworkers, is particularly important, since the reaction conditions are essentially neutral, and so provides a method for acylation of compounds containing an acid-sensitive functionality which would preclude the use of the Friedel-Crafts reaction. Reaction temperatures are often below 100 C, and high (1000-fold) turnovers of the catalyst have been achieved. Solvents employed include chloroform, toluene, and, on occasions, HMPA. Some reactions have been carried out under an atmosphere of carbon monoxide to prevent excessive decarbonylation of the acyl palladium intermediate. Indeed, carbonylative coupling of alkenylstannanes with allyl halides in the presence of carbon monoxide ca. 3 atm or greater 1 atm =101 kPa) offers an alternative to the Friedel-Crafts acylation, ketones being formed by the reaction of the stannane with the acyl species formed by carbon monoxide insertion into the allyl palladium intermediate. ... 

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