Trifluoromethanesulfonyl azide
Names
Preferred IUPAC name
Trifluoromethanesulfonyl azide
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/CF3N3O2S/c2-1(3,4)10(8,9)7-6-5 checkY
    Key: NQPHMXWPDCSHTE-UHFFFAOYSA-N checkY
  • InChI=1/CF3N3O2S/c2-1(3,4)10(8,9)7-6-5
    Key: NQPHMXWPDCSHTE-UHFFFAOYAT
  • FC(F)(F)S(=O)(=O)N=[N+]=[N-]
Properties
CF3SO2N3
Molar mass 175.09 g·mol−1
Melting point 80-81 °C
insoluble[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references

Trifluoromethanesulfonyl azide or triflyl azide CF3SO2N3 is an organic azide used as a reagent in organic synthesis.

Preparation

Trifluoromethanesulfonyl azide is not commercially available. It is prepared before use by reacting trifluoromethanesulfonic anhydride with sodium azide, traditionally in dichloromethane.[1] However, use of dichloromethane should be avoided because sodium azide is known to generate highly explosive azido-chloromethane and diazidomethane in situ by nucleophilic substitution on dichloromethane.[2] Moreover, the volatility of dichloromethane is a liability, as unsolvated triflyl azide is a detonation hazard.[2] The reaction may also be carried out in toluene,[3] acetonitrile, or pyridine.[4]

Tf2O + NaN3 → TfN3 + NaOTf (Tf = CF3SO2)

The trifluoromethanesulfonic anhydride starting material is rather expensive, and the product is explosive, and does not store well. As a result, imidazole-1-sulfonyl azide has been developed as an alternative.[5]

Reactions

Trifluoromethanesulfonyl azide generally converts amines to azides.

See also

References

  1. 1 2 C. J. Cavender & V. J. Shiner (1972). "Trifluoromethanesulfonyl azide. Its reaction with alkyl amines to form alkyl azides". The Journal of Organic Chemistry. 37 (22): 3567–3569. doi:10.1021/jo00795a052.
  2. 1 2 Cavender, C. J.; Shiner, V. J., Jr. J. Org. Chem. (1972), 37, 3567.
  3. ↑ Titz, A.; Radic, Z.; Schwardt, O.; Ernst, B. Tetrahedron Lett. (2006), 47, 2383.
  4. ↑ R.-B. Yan, F. Yang, Y. Wu, L.-H. Zhang and X.-S. Ye (2005). "An efficient and improved procedure for preparation of triflyl azide and application in catalytic diazotransfer reaction". Tetrahedron Letters. 46 (52): 8993–8995. doi:10.1016/j.tetlet.2005.10.103.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ↑ E. D. Goddard-Borger & R. V. Stick (2007). "An Efficient, Inexpensive, and Shelf-Stable Diazotransfer Reagent:  Imidazole-1-sulfonyl Azide Hydrochloride". Organic Letters. 9 (19): 3797–3800. doi:10.1021/ol701581g. PMID 17713918.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.