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Tetrabromo-o-xylene

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Tetrabromo-o-xylene
Names
Preferred IUPAC name 1,2-Bis(dibromomethyl)benzene
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.032.873 Edit this at Wikidata
EC Number
  • 236-176-2
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C8H6Br4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4,7-8HKey: LNAOKZKISWEZNY-UHFFFAOYSA-N
SMILES
  • C1=CC=C(C(=C1)C(Br)Br)C(Br)Br
Properties
Chemical formula C8H6Br4
Molar mass 421.752 g·mol
Appearance off white solid
Melting point 115–116 °C (239–241 °F; 388–389 K)
Hazards
GHS labelling:
Pictograms GHS05: CorrosiveGHS07: Exclamation markGHS09: Environmental hazard
Signal word Danger
Hazard statements H314, H335, H400
Precautionary statements P260, P261, P264, P271, P273, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P363, P391, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

α,α,α',α'-Tetrabromo-o-xylene is an organobromine compound with the formula C6H4(CHBr2)2. Three isomers of α,α,α',α'-Tetrabromoxylene exist, but the ortho derivative is most widely studied. It is an off-white solid. The compound is prepared by the photochemical reaction of o-xylene with elemental bromine:

C6H4(CH3)2 + 4 Br2 → C6H4(CHBr2)2 + 4 HBr

Reaction of α,α,α',α'-tetrabromo-o-xylene with sodium iodide affords α,α'-dibromo-o-xylylene, which can be trapped with dienophiles to give naphthylene. In the absence of trapping agents, the xylylene relaxes to α,α'-dibromobenzocyclobutane:

C6H4(CHBr2)2 + 2 NaI → C6H4(=CHBr)2 + 2 NaBr + I2
C6H4(=CHBr)2 → C6H4(CHBr)2

Cycloadditions of these xylylenes provides a pathway to acenes.

References

  1. Bill, J. C.; Tarbell, D. S. (1954). "o-Phthalaldehyde". Organic Syntheses. 34: 82. doi:10.15227/orgsyn.034.0082.
  2. Cava, M. P.; Deana, A. A.; Muth, K. (1959). "Condensed Cyclobutane Aromatic Compounds. VIII. The Mechanism of Formation of 1,2-Dibromobenzocyclobutene; A New Diels-Alder Synthesis". Journal of the American Chemical Society. 81 (24): 6458–6460. doi:10.1021/ja01533a032.
  3. Paddon-Row, Michael N.; Patney, Harish K. (1986). "An Efficient Synthetic Strategy for Naphthalene Annellation of Norbornenylogous Systems". Synthesis. 1986 (4): 328–330. doi:10.1055/s-1986-31603. S2CID 94212857.
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