Alkylbenzene

• Friedel-Crafts alkylation: alkylbenzenes can be synthesized from olefins or alkyl halides with aromatic compounds in the presence of a catalyst such as AlCl3, HF, or H2SO4. • Gattermann-Koch reaction: named after German chemists Ludwig Gattermann and Julius Arnold Koch, the Gattermann-Koch reaction is a catalyzed formylation of alkylbenzenes with carbon monoxide and hydrochloric acid. • Alkylbenzene sulfonation reaction: electrophilic addition of a sulfonic acid group onto the aromatic ring. == Spectroscopy ==

Alkylbenzene isomers can be differentiated by observing the position of alkyl substituents on the benzene ring using chemical ionization-proton exchange mass spectrometry. Conventional GC-MS yields limited results because the isomers have identical molecular weight and substituents. == Production ==

Some alkylbenzenes such as toluene, trimethylbenzenes, and tetramethylbenzenes occur naturally in coal tar oil and as byproducts of the crude oil refinery process. Others can be prepared by Friedel-Crafts alkylation. Alkylbenzenes used to be synthesized from tetrapropylene, however, the reaction is now rarely used because of the low biodegradable alkylbenzene sulfonates it yields. == Safety hazards ==

Alkylbenzenes are flammable. Most of them are eye and skin irritants and pose an acute health hazard when ingested. Alkylbenzenes are toxic to aquatic life with long-lasting effects. == Application ==

=== Synthetic sulfonates === Alkylbenzenes are the primary raw material in making synthetic alkylbenzene sulfonates. Synthetic sulfonates are the most widely used detergents, as industrial oil, emulsifiers, demulsifiers, rust inhibitors, dispersants, surfactants for enhanced oil recovery, ore-floatation agents, and wetting agents, among others. LABs such as alkylbenzene, dialkylbenzene, and alkyltoluene are most commonly used to prepare sulfonate detergents. Solvent use Some less substituted alkylbenzenes such as toluene and xylene are commonly used as solvents industrially. == Literature ==

• Allinger, Cava, de Jongh, Johnson, Lebel, Stevens: Organische Chemie, 1. Auflage, Walter de Gruyter, Berlin 1980, , pp. 367–368, 560–562. • Streitwieser / Heathcock: Organische Chemie, 1. Auflage, Verlag Chemie, Weinheim 1980, , pp. 1051, 1073–1080. • Beyer / Walter: Lehrbuch der Organischen Chemie, 19. Auflage, S. Hirzel Verlag, Stuttgart 1981, , pp. 442–444. • Morrison / Boyd: Lehrbuch der Organischen Chemie, 3. Auflage, Verlag Chemie, Weinheim 1986, , pp. 707–728. ==References==