Friedel–Crafts reaction

Friedel-Crafts acylation
Named after	Charles Friedel ; James Crafts
Reaction type	Coupling reaction
Identifiers
Organic Chemistry Portal	friedel-crafts-acylation
RSC ontology ID	RXNO:0000045

Friedel-Crafts alkylation
Named after	Charles Friedel ; James Crafts
Reaction type	Coupling reaction
Identifiers
Organic Chemistry Portal	friedel-crafts-alkylation
RSC ontology ID	RXNO:0000046

Friedel-Crafts reaction
Named after	Charles Friedel ; James Crafts
Reaction type	Coupling reaction
Identifiers
RSC ontology ID	RXNO:0000369

The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring.^[1] Friedel–Crafts reactions are of two main types: alkylation reactions and acylation reactions. Both proceed by electrophilic aromatic substitution.^[2]^[3]^[4]^[5]

Friedel–Crafts alkylation

Friedel–Crafts alkylation involves the alkylation of an aromatic ring with an alkyl halide using a strong Lewis acid catalyst.^[6] With anhydrous ferric chloride as a catalyst, the alkyl group attaches at the former site of the chloride ion. The general mechanism is shown below.^[7]

This reaction suffers from the disadvantage that the product is more nucleophilic than the reactant. Consequently, overalkylation occurs. Furthermore, the reaction is only very useful for tertiary alkylating agents, some secondary alkylating agents, or ones that yield stabilized carbocations (e.g., benzylic ones). In the case of primary alkyl halides, the incipient carbocation (R⁽⁺⁾---X---Al^(-)Cl₃) will undergo a carbocation rearrangement reaction.^[7]

Steric hindrance can be exploited to limit the number of alkylations, as in the t-butylation of 1,4-dimethoxybenzene.^{[citation needed]}

Alkylations are not limited to alkyl halides: Friedel–Crafts reactions are possible with any carbocationic intermediate such as those derived from alkenes and a protic acid, Lewis acid, enones, and epoxides. An example is the synthesis of neophyl chloride from benzene and methallyl chloride:^[8]

H₂C=C(CH₃)CH₂Cl + C₆H₆ → C₆H₅C(CH₃)₂CH₂Cl

In one study the electrophile is a bromonium ion derived from an alkene and NBS:^[9]

In this reaction samarium(III) triflate is believed to activate the NBS halogen donor in halonium ion formation.

Friedel–Crafts dealkylation

Friedel–Crafts alkylation has been hypothesized to be reversible. In a reversed Friedel–Crafts reaction or Friedel–Crafts dealkylation, alkyl groups are removed in the presence of protons or other Lewis acid.^{[citation needed]}

For example, in a multiple addition of ethyl bromide to benzene, ortho and para substitution is expected after the first monosubstitution step because an alkyl group is an activating group. However, the actual reaction product is 1,3,5-triethylbenzene with all alkyl groups as a meta substituent.^[10] Thermodynamic reaction control makes sure that thermodynamically favored meta substitution with steric hindrance minimized takes prevalence over less favorable ortho and para substitution by chemical equilibration. The ultimate reaction product is thus the result of a series of alkylations and dealkylations.^{[citation needed]}

Friedel–Crafts acylation

Friedel–Crafts acylation involves the acylation of aromatic rings.^[11] Typical acylating agents are acyl chlorides. Typical Lewis acid catalysts are acids and aluminium trichloride. Friedel–Crafts acylation is also possible with acid anhydrides.^[12] Reaction conditions are similar to the Friedel–Crafts alkylation. This reaction has several advantages over the alkylation reaction. Due to the electron-withdrawing effect of the carbonyl group, the ketone product is always less reactive than the original molecule, so multiple acylations do not occur. Also, there are no carbocation rearrangements, as the acylium ion is stabilized by a resonance structure in which the positive charge is on the oxygen.

The viability of the Friedel–Crafts acylation depends on the stability of the acyl chloride reagent. Formyl chloride, for example, is too unstable to be isolated. Thus, synthesis of benzaldehyde via the Friedel–Crafts pathway requires that formyl chloride be synthesized in situ. This is accomplished via the Gattermann-Koch reaction, accomplished by treating benzene with carbon monoxide and hydrogen chloride under high pressure, catalyzed by a mixture of aluminium chloride and cuprous chloride.

Reaction mechanism

The reaction proceeds via generation of an acylium center:

The reaction is completed by deprotonation of the arenium ion by AlCl₄⁻, regenerating the AlCl₃ catalyst:

If desired, the resulting ketone can be subsequently reduced to the corresponding alkane substituent by either Wolff–Kishner reduction or Clemmensen reduction. The net result is the same as the Friedel–Crafts alkylation except that rearrangement is not possible.^[13]

Friedel–Crafts hydroxyalkylation

Arenes react with certain aldehydes and ketones to form the hydroxyalkylated products, for example in the reaction of the mesityl derivative of glyoxal with benzene:^[14]

As usual, the aldehyde group is more reactive electrophile than the phenone.

Scope and variations

This reaction is related to several classic named reactions:

The acylated reaction product can be converted into the alkylated product via a Clemmensen reduction.^[15]^[16]^[17]
The Gattermann–Koch reaction can be used to synthesize benzaldehyde from benzene.^[18]
The Gatterman reaction describes arene reactions with hydrocyanic acid.^[19]
The Houben–Hoesch reaction describes arene reactions with nitriles.^[20]^[21]
A reaction modification with an aromatic phenyl ester as a reactant is called the Fries rearrangement.
In the Scholl reaction two arenes couple directly (sometimes called Friedel–Crafts arylation).^[22]^[23]
In the Zincke–Suhl reaction p-cresol is alkylated to a cyclohexadienone with tetrachloromethane.^[24]
In the Blanc chloromethylation a chloromethyl group is added to an arene with formaldehyde, hydrochloric acid and zinc chloride.^[25]^[26]
The Bogert–Cook synthesis (1933) involves the dehydration and isomerization of 1-β-phenylethylcyclohexanol to the octahydro derivative of phenanthrene^[27]

The Darzens–Nenitzescu synthesis of ketones (1910, 1936) involves the acylation of cyclohexene with acetyl chloride to methylcyclohexenylketone.
In the related Nenitzescu reductive acylation (1936) a saturated hydrocarbon is added making it a reductive acylation to methylcyclohexylketone
The Nencki reaction (1881) is the ring acetylation of phenols with acids in the presence of zinc chloride.^[28]
In a green chemistry variation aluminium chloride is replaced by graphite in an alkylation of p-xylene with 2-bromobutane. This variation will not work with primary halides from which less carbocation involvement is inferred.^[29]

Dyes

Friedel–Crafts reactions have been used in the synthesis of several triarylmethane and xanthene dyes.^[30] Examples are the synthesis of thymolphthalein (a pH indicator) from two equivalents of thymol and phthalic anhydride:

A reaction of phthalic anhydride with resorcinol in the presence of zinc chloride gives the fluorophore Fluorescein. Replacing resorcinol by N,N-diethylaminophenol in this reaction gives rhodamine B:

Haworth reactions

The Haworth reaction is a classic method for the synthesis of 1-tetralone.^[31] In it benzene is reacted with succinic anhydride, the intermediate product is reduced and a second FC acylation takes place with addition of acid.^[32]

In a related reaction, phenanthrene is synthesized from naphthalene and succinic anhydride in a series of steps.

Friedel–Crafts test for aromatic hydrocarbons

Reaction of chloroform with aromatic compounds using an aluminium chloride catalyst gives triarylmethanes, which are often brightly colored, as is the case in triarylmethane dyes. This is a bench test for aromatic compounds.^[33]

References

^ Friedel, C.; Crafts, J. M. (1877) "Sur une nouvelle méthode générale de synthèse d’hydrocarbures, d’acétones, etc.," Compt. Rend., 84: 1392 & 1450.
^ Price, C. C. (1946). "The Alkylation of Aromatic Compounds by the Friedel-Crafts Method". Org. React. 3: 1. doi:10.1002/0471264180.or003.01. ISBN 0471264180.
^ Groves, J. K. (1972). "The Friedel–Crafts acylation of alkenes". Chem. Soc. Rev. 1: 73. doi:10.1039/cs9720100073.
^ Eyley, S. C. (1991). "The Aliphatic Friedel–Crafts Reaction". Compr. Org. Synth. 2: 707–731. doi:10.1016/B978-0-08-052349-1.00045-7. ISBN 978-0-08-052349-1.
^ Heaney, H. (1991). "The Bimolecular Aromatic Friedel–Crafts Reaction". Compr. Org. Synth. 2: 733–752. doi:10.1016/B978-0-08-052349-1.00046-9. ISBN 978-0-08-052349-1.
^ Rueping, M.; Nachtsheim, B. J. (2010). "A review of new developments in the Friedel–Crafts alkylation – From green chemistry to asymmetric catalysis". Beilstein J. Org. Chem. 6 (6). doi:10.3762/bjoc.6.6.
^ ^a ^b Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 978-0-471-72091-1
^ Smith, W. T. Jr. and Sellas, J. T. (1963). "Neophyl chloride". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link).
^ Hajra, S.; Maji, B.; Bar, S. (2007). "Samarium Triflate-Catalyzed Halogen-Promoted Friedel–Crafts Alkylation with Alkenes". Org. Lett. 9 (15): 2783–2786. doi:10.1021/ol070813t.
^ Anslyn, E.; Wallace, K. J.; Hanes, R.; Morey, J.; Kilway, K. V.; Siegel, J. (2005). "Preparation of 1,3,5-Tris(aminomethyl)-2,4,6-triethylbenzene from Two Versatile 1,3,5-Tri(halosubstituted) 2,4,6-Triethylbenzene Derivatives". Synthesis. 2005 (12): 2080–2083. doi:10.1055/s-2005-869963.
^ Catalytic Friedel–Crafts Acylation Reactions, Chapter 3; Sartori, G.; Maggi, R.; Santacroce, V. (2016). Arene Chemistry: Reaction Mechanisms and Methods for Aromatic Compounds (J. Mortier Ed.). John Wiley & Sons. pp. 69–82. doi:10.1002/9781118754887. ISBN 978-1-118-75498-6.{{cite book}}: CS1 maint: numeric names: authors list (link)
^ Somerville, L. F.; Allen, C. F. H. (1933). "β-Benzoylpropionic acid". Organic Syntheses. 13: 12. doi:10.15227/orgsyn.013.0012.
^ Friedel-Crafts Acylation. Organic-chemistry.org. Retrieved on 2014-01-11.
^ Fuson, R. C.; Weinstock, H. H.; Ullyot, G. E. (1935). "A New Synthesis of Benzoins. 2′,4′,6′-Trimethylbenzoin". J. Am. Chem. Soc. 57 (10): 1803–1804. doi:10.1021/ja01313a015.
^ Clemmensen, E. (1913). "Reduktion von Ketonen und Aldehyden zu den entsprechenden Kohlenwasserstoffen unter Anwendung von amalgamiertem Zink und Salzsäure". Chemische Berichte. 46: 1837–1843. doi:10.1002/cber.19130460292.
^ Clemmensen, E. (1914). "Über eine allgemeine Methode zur Reduktion der Carbonylgruppe in Aldehyden und Ketonen zur Methylengruppe". Chemische Berichte. 47: 51–63. doi:10.1002/cber.19140470108.
^ Clemmensen, E. (1914). "Über eine allgemeine Methode zur Reduktion der Carbonylgruppe in Aldehyden und Ketonen zur Methylengruppe. (III. Mitteilung.)". Chemische Berichte. 47: 681–687. doi:10.1002/cber.191404701107.
^ Gattermann, L.; Koch, J. A. (1897). "Eine Synthese aromatischer Aldehyde". Ber. 30: 1622–1624. doi:10.1002/cber.18970300288.
^ L. Gattermann; W. Berchelmann (1898). "Synthese aromatischer Oxyaldehyde". Berichte der deutschen chemischen Gesellschaft. 31 (2): 1765–1769. doi:10.1002/cber.18980310281.
^ Hoesch, Kurt (1915). "Eine neue Synthese aromatischer Ketone. I. Darstellung einiger Phenol-ketone". Berichte der deutschen chemischen Gesellschaft. 48 (1): 1122–1133. doi:10.1002/cber.191504801156.
^ J. Houben (1926). Über die Kern-Kondensation von Phenolen und Phenol-äthern mit Nitrilen zu Phenol- und Phenol-äther-Ketimiden und -Ketonen (I.). Berichte der deutschen chemischen Gesellschaft (A and B Series) 59 (11) 2878–2891. doi:10.1002/cber.19260591135
^ M B Smith, J March. March's Advanced Organic Chemistry (Wiley, 2001) (ISBN 0-471-58589-0)
^ Grzybowski, M.; Skonieczny, K.; Butenschön, H.; Gryko, D. T. (2013). "Comparison of Oxidative Aromatic Coupling and the Scholl Reaction". Angew. Chem. Int. Ed. 52: 9900–9930. doi:10.1002/anie.201210238.
^ Zincke, Th.; Suhl. R. (1906). "Ueber die Einwirkung von Tetrachlorkohlenstoff und Aluminiumchlorid auf p-Kresol und p-Kresolderivate". Chemische Berichte. 39 (4): 4148–4153. doi:10.1002/cber.190603904115.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^ Blanc, Gustave Louis (1923). Bulletin de la Société chimique de France [4]. 33: 313–319. {{cite journal}}: Missing or empty |title= (help)
^ G. Grassi and C. Maselli (1898) "Su alcuni derivati clorurati de trossimetilene" (On some chlorinated derivatives of 1,3,5-trioxane), Gazzetta Chimica Italiana, 28 (part 2) : 477-500 ; see especially p. 495.
^ This reaction with phosphorus pentoxide: Kamp, J. V. D.; Mosettig, E. (1936). "Trans- and Cis-As-Octahydrophenanthrene". Journal of the American Chemical Society. 58 (6): 1062–1063. doi:10.1021/ja01297a514.
^ Nencki, M.; Sieber, N. (1881). "Ueber die Verbindungen der ein- und zweibasischen Fettsäuren mit Phenolen". J. Prakt. Chem. (in German). 23: 147–156. doi:10.1002/prac.18810230111.
^ Sereda, Grigoriy A.; Rajpara, Vikul B. (2007). "A Green Alternative to Aluminum Chloride Alkylation of Xylene". J. Chem. Educ. 2007 (84): 692. Bibcode:2007JChEd..84..692S. doi:10.1021/ed084p692.
^ McCullagh, James V.; Daggett, Kelly A. (2007). "Synthesis of Triarylmethane and Xanthene Dyes Using Electrophilic Aromatic Substitution Reactions". J. Chem. Educ. 84: 1799. doi:10.1021/ed084p1799.
^ Haworth, Robert Downs (1932). "Syntheses of alkylphenanthrenes. Part I. 1-, 2-, 3-, and 4-Methylphenanthrenes". J. Chem. Soc.: 1125. doi:10.1039/JR9320001125.
^ Li, Jie Jack (2003) Name Reactions: A Collection of Detailed Reaction Mechanisms, Springer, ISBN 3-540-40203-9, p. 175.
^ John C. Gilbert., Stephen F. Martin. Experimental Organic Chemistry: A Miniscale and Microscale Approach^{[permanent dead link‍]}. Brooks/Cole CENGAGE Learning, 2011. pp 872. 25.10 Aromatic Hydrocarbons and Aryl Halides - Classification test. ISBN 978-1-4390-4914-3