2,6-Dimethylnaphthalene

2,6-Dimethylnaphthalene
Names
	IUPAC name 2,6-Dimethylnaphthalene
Identifiers
CAS Number	581-42-0 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:34251;
ChemSpider	10909;
ECHA InfoCard	100.008.605
PubChem CID	11387;
UNII	76U29QW3FM ;
CompTox Dashboard (EPA)	DTXSID0029187 ;
	InChI InChI=1S/C12H12/c1-9-3-5-12-8-10(2)4-6-11(12)7-9/h3-8H,1-2H3 Key: YGYNBBAUIYTWBF-UHFFFAOYSA-N; InChI=1/C12H12/c1-9-3-5-12-8-10(2)4-6-11(12)7-9/h3-8H,1-2H3 Key: YGYNBBAUIYTWBF-UHFFFAOYAZ;
	SMILES Cc1ccc2cc(ccc2c1)C;
Properties
Chemical formula	C12H12
Molar mass	156.228 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

2,6-Dimethylnaphthalene (2,6-DMN) is a polycyclic aromatic hydrocarbon. It is one of the ten dimethylnaphthalene isomers, which are derived from naphthalene by the addition of two methyl groups. 2,6-DMN is of commercial importance as a starting material for high-performance polyester fibers and films. Polyethylene naphthalate (PEN) is made from the product of oxidation 2,6-DMN.^[1]

Synthesis

Alkylated naphthalenes (methyl-, dimethyl-, and poly-methyl naphthalenes, thus including 2,6-DMN) are found in low concentrations in crude oil and coal tar. Separation is difficult, expensive, and requires a number of operations such as selective crystallization and adsorption, in addition to any isomerization reactions.^[2] There has been a search for suitable synthetic routes to 2,6-DMN.

In the "alkenylation process" butadiene (1) , o-xylene (2), and Sodium-potassium alloy (3) are used, which react to form 5-(ortho-tolyl)pent-2-ene (OTP, 3).^[3] OTP is subsequently cyclized to 1,5-dimethyltetraline (4). Dehydrogenation then provides 1,5-dimethylnaphthalene (1,5-DMN, 5). Finally, 1,5-DMN is isomerized to 2,6-DMN (6). In the final step, other mono-, di-, and tri-methylnaphthalenes are formed. More work is therefore required in separation of the mixture, which is done by selective crystallization.

Applications

2,6-Dimethylnaphthalene is mainly used for the preparation of 2,6-naphthalenedicarboxylic acid by oxidation of 2,6-dimethylnaphthalene in the liquid phase. 2,6-Naphthalenedicarboxylic acid is a monomer for the production of high-performance polymers, in particular poly (ethylene-2,6-naphthalene dicarboxylate) or shorter polyethylene naphthalate (PEN), a polyester which is stronger and has a higher thermal resistance than the frequently used polyethylene terephthalate (PET). However, 2,6-DMN is a more expensive intermediate than terephthalic acid that is used for PET.

References

^ Lillwitz, L. D. (2001). "Production of Dimethyl-2,6-Naphthalenedicarboxylate: Precursor to Polyethylene Naphthalate". Applied Catalysis A: General. 221: =337–358. doi:10.1016/S0926-860X(01)00809-2.{{cite journal}}: CS1 maint: extra punctuation (link)
^ US patent 5004853, Paul T. Barger, Timothy J. Barder, David Y. Lin, Simon H. Hobbs, "Continuous process for the production of 2,6-dimethylnaphthalene", issued April 2, 1991
^ US patent, Lawrence D. Lillwitz, Anne M. Karachewski, "Alkylation of alkylaromatics promoted by sonicated alkali metal", issued March 30, 1993

[1] Lillwitz, L. D. (2001). "Production of Dimethyl-2,6-Naphthalenedicarboxylate: Precursor to Polyethylene Naphthalate". Applied Catalysis A: General. 221: =337–358. doi:10.1016/S0926-860X(01)00809-2.{{cite journal}}: CS1 maint: extra punctuation (link)

[2] US patent 5004853, Paul T. Barger, Timothy J. Barder, David Y. Lin, Simon H. Hobbs, "Continuous process for the production of 2,6-dimethylnaphthalene", issued April 2, 1991

[3] US patent, Lawrence D. Lillwitz, Anne M. Karachewski, "Alkylation of alkylaromatics promoted by sonicated alkali metal", issued March 30, 1993

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