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Tetraphenylmethane

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Tetraphenylmethane
Names
Preferred IUPAC name 1,1′,1′′,1′′′-Methanetetrayltetrabenzene
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.010.132 Edit this at Wikidata
EC Number
  • 211-144-0
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C25H20/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20HKey: PEQHIRFAKIASBK-UHFFFAOYSA-N
  • InChI=1/C25H20/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20HKey: PEQHIRFAKIASBK-UHFFFAOYAS
SMILES
  • c1ccccc1C(c2ccccc2)(c3ccccc3)c4ccccc4
Properties
Chemical formula C25H20
Molar mass 320.44 g/mol
Melting point 282 °C (540 °F; 555 K)
Boiling point 431 °C
Structure
Crystal structure tetragonal
Space group P421c, No. 114
Point group S4
Lattice constant a = 10.896 Å, c = 7.280 Å(20 °C)
Formula units (Z) 2
Hazards
GHS labelling:
Pictograms GHS08: Health hazard
Signal word Danger
Hazard statements H350
Precautionary statements P201, P202, P281, P308+P313, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Tetraphenylmethane is an organic compound consisting of a methane core with four phenyl substituents. It was first synthesized by Moses Gomberg in 1898.

Synthesis

Gomberg's classical organic synthesis shown below starts by reacting triphenylmethyl bromide 1 with phenylhydrazine 2 to the hydrazine 3. Oxidation with nitrous acid then produces the azo compound 4 from which on heating above the melting point, nitrogen gas evolves with formation of tetraphenylmethane 5.

Gomberg's tetraphenylmethane synthesis

Gomberg was able to distinguish this compound from triphenylmethane (elemental analysis was not an option given the small differences in the hydrogen fractions of 6.29% and 6.60%) by nitration of 5 with nitric acid to 6. A strong base would be able to abstract the methine proton of the nitrated triphenylmethyl compound if present, forming a strongly colored compound.

He obtained further evidence for the formation of tetraphenylmethane by reducing the nitro groups to amino groups with zinc dust in acetic acid to the leuco dye 7, which on exposure to hydrochloric acid eliminates aniline to the known compound pararosaniline 8.

Gomberg's success in synthesizing tetraphenylmethane set him on the attempt to prepare the next homologue hexaphenylethane, which led him to the discovery of the triphenylmethyl radical.

See also

References

  1. Robbins, A.; Jeffrey, G. A.; Chesick, J. P.; Donohue, J.; Cotton, F. A.; Frenz, B. A.; Murillo, C. A. (1975-10-01). "A refinement of the crystal structure of tetraphenylmethane: three independent redeterminations". Acta Crystallographica Section B: Structural Crystallography and Crystal Chemistry. 31 (10): 2395–2399. Bibcode:1975AcCrB..31.2395R. doi:10.1107/S0567740875007686. ISSN 0567-7408.
  2. Gomberg, M. (1898). "On tetraphenylmethane". J. Am. Chem. Soc. 20 (10): 773–780. doi:10.1021/ja02072a009.
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