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. Author manuscript; available in PMC: 2015 Oct 11.
Published in final edited form as: Chem Commun (Camb). 2014 Oct 11;50(79):11701–11704. doi: 10.1039/c4cc05650g

Table 2.

Effects of the catalyst on the fluorination of 5[a]

graphic file with name nihms622911t2.jpg

Entry 5 (equiv) ketone catalyst Yield[b]
1 23 graphic file with name nihms622911t3.jpg R = CH3, X = H 90%
2 23 R = CH3, X = OMe 82%
3 23 R = CH3, X = NO2 18%
4 23 R = CF3, X = H 63%
5 23 R = H, X = H 59%

6 23 graphic file with name nihms622911t4.jpg X = H 78%
7 23 X = OMe 76%
8 23 X = NMe2 17%

9 23 graphic file with name nihms622911t5.jpg X = – 75%
10 23 X = O 87%
11 5 X = O 81%

12 5 graphic file with name nihms622911t6.jpg 88%
13 1.5 76%
14 1.0 59%
[a]

Reaction conditions: 0.01 mmol catalyst, 0.2 mmol Selectfluor, 2 mL CH3CN.

[b]

Determined by 19F NMR using C6H5F as an external standard.