Processes alkylbenzene process chemistry

The following HF alkylation reactions are based on straight-chain olefins. A similar chemistry can be written for the branched-chain process. The main reaction is the alkylation of benzene with the straight-chain olefins to yield a linear alkylbenzene ... 

Not only the linear Cl0-Cl8 a-olefins but also the linear C10-Cl8 olefins with internal double bonds, the so-called -v /-olefins, are of great importance in surfactant chemistry, n-a-Olefins and n-y-olefins have the same suitability for the manufacture of linear alkylbenzenes, the most important synthetic anionic surfactants, by alkylation of benzene. Nowadays medium molecular weight n- /-olefins are industrially produced by two processes the catalytic dehydrogenation of the corresponding n-alkanes [4,28] and the cometathesis of low and high molecular weight n-v /-olefins, obtained by double-bond isomerization of the isomeric n-a-olefins [29]. 

The oldest surfactant is soap, which may be traced back to the ancient Egyptians and beyond. Synthetic surfactants had been produced in the first half of the 20th century but it was only after World War II, with the development of the modern petrochemical industry, that alternative feedstocks to oleochemicals became readily available. Hence chloroparaf-fins and/or alphaolefins and benzene were used to produce alkylbenzene (or alkylate ), processes were developed to produce a range of synthetic fatty alcohols and alkylene oxide chemistry resulted in ethylene oxide and propylene oxide building blocks becoming readily available. 

None of the electrophilic substitutions mentioned so far has led to carbon-carbon bond formation, one of the primary challenges in organic chemistry. In principle, such reactions could be carried out with benzene in the presence of a sufQciently electrophilic carbon-based electrophile. This section introduces the first of two such transformations, the Friedel-Crafts reactions. The secret to the success of both processes is the use of a Lewis acid, usually aluminum chloride. In the presence of this reagent, haloalkanes attack benzene to form alkylbenzenes. 

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