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Selectfluor™ Reagent

Selectfluor™ (1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate), or F-TEDA) is a user-friendly, mild, air- and moisture-stable, non-volatile reagent for electrophilic fluorination. Selectfluor™ reagent is capable of introducing fluorine into organic substrates in one step, with a remarkably broad scope of reactivity.1 Many of these reactions display excellent regioselectivity.

The synthesis of a potent and noncytotoxic nucleoside inhibitor of Hepatitis C virus RNA replication was accomplished using Selectfluor™ Reagent (Scheme 1). This ribonucleoside shows a significantly improved enzymatic stability profile compared to the parent 2’-C-methyladenosine.2

Selectfluor™

Scheme 1.

Allylic fluorides can be prepared via a sequential cross-metathesis/ electrophilic fluorodesilylation route (Scheme 2). This route avoids the formation of by-products that result from allylic transposition, which is observed when nucleophilic displacement or ring-opening reaction with DAST is attempted.3

Allylic fluorides

Scheme 2.

Selectfluor™ reagent is also capable of effecting other transformations. One example uses Selectfluor™ reagent as an alternative to silver or mercury salts in the rearrangement of iodides to alcohols (Scheme 3). In the case of an iodochloride (X=Cl), substitution only occurs at the iodide and not the chloride.4

rearrangement of iodides

Scheme 3.

Selectfluor™ reagent has been used as an efficient catalyst for the preparation of b-hydroxy thiocyanates using ammonium thiocyanate under mild conditions (Scheme 4). In all cases, the reactions proceed rapidly at room temperature without the formation of the corresponding thiiranes, which are generally the exclusive products when Lewis acids such as Sc(OTf)3 and InCl3 are used.5

b-hydroxy thiocyanates

Scheme 4.

References

1.
Singh, R. P. , Shreeve, J. M.. 2004. For a review of recent highlights: Acc. Chem. Res..37, 31.
2.
Eldrup AB, Prhavc M, Brooks J, Bhat B, Prakash TP, Song Q, Bera S, Bhat N, Dande P, Cook PD, et al. 2004. Structure?Activity Relationship of Heterobase-Modified 2?-C-Methyl Ribonucleosides as Inhibitors of Hepatitis C Virus RNA Replication. J. Med. Chem.. 47(21):5284-5297. http://dx.doi.org/10.1021/jm040068f
3.
Thibaudeau S, Gouverneur V. 2003. Sequential Cross-Metathesis/Electrophilic Fluorodesilylation:? A Novel Entry to Functionalized Allylic Fluorides. Org. Lett.. 5(25):4891-4893. http://dx.doi.org/10.1021/ol035991a
4.
Krow GR, Lin G, Moore KP, Thomas AM, DeBrosse C, Ross CW, Ramjit HG. 2004. Novel Selectfluor and Deoxo-Fluor-Mediated Rearrangements. New 5(6)-Methyl and Phenyl Methanopyrrolidine Alcohols and Fluorides. Org. Lett.. 6(10):1669-1672. http://dx.doi.org/10.1021/ol0494818
5.
Yadav J, Reddy B, Reddy C. 2004. Selectfluor?: a novel and efficient reagent for the synthesis of ?-hydroxy thiocyanates. Tetrahedron Letters. 45(6):1291-1293. http://dx.doi.org/10.1016/j.tetlet.2003.11.102