The importance of selectively fluorinating compounds in medicinal chemistry, biology, and organic synthesis is well appreciated and provides a major impetus to the discovery of new and mild fluorinating agents that can operate safely and efficiently. Elemental fluorine and many electrophilic fluorinating agents have been used in synthesis; however, most of these fluorinating agents are highly aggressive, unstable, and require special equipment and care for safe handling. Sigma-Aldrich is pleased to offer the following alternatives, which lack these drawbacks.

4-Iodotoluene Difluoride (Tol-IF2)

4-Iodotoluene difluoride (Tol-IF2) is easy to handle and less toxic than many fluorinating agents. Selective monofluorination of b-keto esters, b-keto amides, and b-diketones takes place under mild conditions without the use of HF–amine complexes.1 A new methodology for the synthesis of fluorinated cyclic ethers was recently reported, which utilized Tol-IF2 to achieve a fluorinative ring-expansion of four-, five-, and six-membered rings.2 When one equivalent of Tol-IF2 is reacted with phenylsulfanylated esters, the afluoro sulfide results through a fluoro-Pummerer reaction.3 When phenylsulfanylated lactams were treated with two equivalents of Tol-IF2, the lactams were fluorinated in the a and b positions, resulting in diastereomeric difluorides.4

4-Iodotoluene difluoride

Selectfluor™ Fluorinating Reagent (F-TEDA)

Selectfluor™ fluorinating reagent [(1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2] octane bis(tetrafluoroborate), or F-TEDA)] is a user friendly, mild, air- and moisturestable, non-volatile reagent for electrophilic fluorination. Selectfluor™ is capable of introducing fluorine into organic substrates in one step, with a remarkably broad scope of reactivity, often with excellent regioselectivity.5 For example, allylic fluorides can be prepared using Selectfluor™ via a sequential cross-metathesis–electrophilic fluorodesilylation route. This route avoids the formation of byproducts that result from allylic transposition, which is observed when nucleophilic displacement or ring-opening reaction with DAST is attempted.6

Selectfluor™ Fluorinating Reagent
Materials
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References

1.
Masanori Y, Komei F, Saeko S, Shoji H. α-Fluorination of β-dicarbonyl compounds using p-iodotoluene difluoride under neutral conditions. 2003(6):36. http://dx.doi.org/10.3998/ark.5550190.0004.605
2.
Inagaki T, Nakamura Y, Sawaguchi M, Yoneda N, Ayuba S, Hara S. 2003. Fluorinative ring-expansion of cyclic ethers using p-iodotoluene difluoride. Stereoselective synthesis of fluoro cyclic ethers. Tetrahedron Letters. 44(21):4117-4119. http://dx.doi.org/10.1016/s0040-4039(03)00841-4
3.
Motherwell WB, Greaney MF, Tocher DA. Fluorination of ?-phenylsulfanyl esters using difluoroiodotoluene. J. Chem. Soc., Perkin Trans. 1.(24):2809-2815. http://dx.doi.org/10.1039/b209079a
4.
Greaney MF, Motherwell WB, Tocher DA. 2001. Studies on the additive fluoro-Pummerer reaction of phenylsulfanylated lactams with difluoroiodotoluene. Tetrahedron Letters. 42(48):8523-8526. http://dx.doi.org/10.1016/s0040-4039(01)01813-5
5.
Singh RP, Shreeve JM. 2004. Recent Highlights in Electrophilic Fluorination with 1-Chloromethyl-4-fluoro- 1,4-diazoniabicyclo[2.2.2]octane Bis(tetrafluoroborate). Acc. Chem. Res.. 37(1):31-44. http://dx.doi.org/10.1021/ar030043v
6.
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

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