Chemistry:Trifluoromethanesulfonyl azide
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| Names | |||
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| Preferred IUPAC name
Trifluoromethanesulfonyl azide | |||
| Identifiers | |||
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| Properties | |||
| CF 3SO 2N 3 | |||
| Molar mass | 175.09 g·mol−1 | ||
| Boiling 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). | |||
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Tracking categories (test):
Trifluoromethanesulfonyl azide or triflyl azide CF
3SO
2N
3 is an organic azide used as a reagent in organic synthesis.[2]
Preparation
Trifluoromethanesulfonyl azide is prepared by treating trifluoromethanesulfonic anhydride with sodium azide, traditionally in dichloromethane.[1] However, the use of dichloromethane is avoided since it can generate highly explosive azido-chloromethane and diazidomethane. The reaction may also instead be conducted in toluene,[3] acetonitrile, or pyridine.[4]
- Tf
2O + NaN
3 → TfN
3 + NaOTf (Tf = CF
3SO
2)
An alternative route starts from imidazole-1-sulfonyl azide.[5]
Reactions
Trifluoromethanesulfonyl azide generally converts amines to azides.
See also
References
- ↑ 1.0 1.1 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.
- ↑ Bernet, Bruno; Vasella, Andrea; Liu, Qi; Tor, Yitzhak (2009). "Trifluoromethanesulfonyl Azide". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rn00114.pub2. ISBN 978-0-471-93623-7.
- ↑ Titz, A.; Radic, Z.; Schwardt, O.; Ernst, B. Tetrahedron Lett. (2006), 47, 2383.
- ↑ 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.
- ↑ 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.
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