Mesitylene

Mesitylene is prepared by transalkylation of xylene over solid acid catalyst:^[4]

2 C₆H₄(CH₃)₂ ⇌ C₆H₃(CH₃)₃ + C₆H₅CH₃

C₆H₄(CH₃)₂ + CH₃OH → C₆H₃(CH₃)₃ + H₂O

Although impractical, it could be prepared by trimerization of propyne, also requiring an acid catalyst, which yields a mixture of 1,3,5- and 1,2,4-trimethylbenzenes.

Trimerization of acetone via aldol condensation, which is catalyzed and dehydrated by sulfuric acid is another method of synthesizing mesitylene.^[5]

Oxidation of mesitylene with nitric acid yields trimesic acid, C₆H₃(COOH)₃. Using manganese dioxide, a milder oxidising agent, 3,5-dimethylbenzaldehyde is formed. Mesitylene is oxidised by trifluoroperacetic acid to produce mesitol (2,4,6-trimethylphenol).^[6] Bromination occurs readily, giving mesityl bromide:^[7]

(CH₃)₃C₆H₃ + Br₂ → (CH₃)₃C₆H₂Br + HBr

Mesitylene is a ligand in organometallic chemistry, one example being the organomolybdenum complex [(η⁶-C₆H₃Me₃)Mo(CO)₃]^[8] which can be prepared from molybdenum hexacarbonyl.

Mesitylene is mainly used as a precursor to 2,4,6-trimethylaniline, a precursor to colorants. This derivative is prepared by selective mononitration of mesitylene, avoiding oxidation of the methyl groups.^[9]

Niche uses

Mesitylene is used in the laboratory as a specialty solvent. In the electronics industry, mesitylene has been used as a developer for photopatternable silicones due to its solvent properties.

The three aromatic hydrogen atoms of mesitylene are in identical chemical shift environments. Therefore, they only give a single peak near 6.8 ppm in the ¹H NMR spectrum; the same is also true for the nine methyl protons, which give a singlet near 2.3 ppm. For this reason, mesitylene is sometimes used as an internal standard in NMR samples that contain aromatic protons.^[10]

One synthesis of uvitic acid obtains the product by oxidizing mesitylene.^[11]

Laboratory quantities of mesitaldehyde are sometimes prepared from mesitylene in a Gattermann reaction variant.^[12]

Mesitylene was first prepared in 1837 by Robert Kane, an Irish chemist, by heating acetone with concentrated sulfuric acid.^[13] He named his new substance "mesitylene" because the German chemist Carl Reichenbach had named acetone "mesit" (from the Greek μεσίτης, the mediator),^[14] and Kane believed that his reaction had dehydrated mesit, converting it to an alkene, "mesitylene".^[15] However, Kane's determination of the chemical composition ("empirical formula") of mesitylene was incorrect. An accurate elemental analysis was provided by August W. von Hofmann in 1849, although von Hofmann also mistook the empirical formula because he used a then-current atomic weight of 6 for carbon.^[16] In 1866 Adolf von Baeyer gave a correct empirical formula, but proposed a tetracyclo[3.1.1.1^1,3.1^3,5]nonane structure:^[17]

Finally, Albert Ladenburg provided conclusive proof that mesitylene was trimethylbenzene in 1874, which he wrote in terms of Ladenburg benzene (see Benzene § Ring formula):^[18]

The group (CH₃)₃C₆H₂- is called mesityl (organic group symbol: Mes). Mesityl derivatives, e.g. tetramesityldiiron, are typically prepared from the Grignard reagent (CH₃)₃C₆H₂MgBr.^[19] Due to its large steric demand, the mesityl group is used as a large blocking group in asymmetric catalysis (to enhance diastereo- or enantioselectivity) and organometallic chemistry (to stabilize low oxidation state or low coordination number metal centers). Larger analogues with even greater steric demand, for example 2,6-diisopropylphenyl (Dipp) and the analogously named Tripp ((ⁱPr)₃C₆H₂, Is) and supermesityl ((^tBu)₃C₆H₂, Mes*) groups, may be even more effective toward achieving these goals.

Mesitylene is also a major urban volatile organic compound (VOC) which results from combustion. It plays a significant role in aerosol and tropospheric ozone formation as well as other reactions in atmospheric chemistry.^{[citation needed]}