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. Author manuscript; available in PMC: 2011 Aug 6.
Published in final edited form as: Org Lett. 2010 Aug 6;12(15):3352–3355. doi: 10.1021/ol101154h

Table 2.

Yields of fluorinated arenes obtained from decomposition of salts 1-7 after removal of TMAPF6.

“Salt Free” Conditions
Cmpd. C6D6
(ArF + 4FA)a
CD3CN
(ArF + 4FA)
1 86 43
2 (77 + 14) (30 + 8)
3 (49 + 23) (40 + 20)
4 (78 + 12) (49 + 32)
5 (57 + 20) (40 + 15)
6 (85 + 10) (68 + 0)
7 (89 + 0) (78 + 0)
a

The numbers inside the parentheses indicate the percentage yields of the desired fluorinated arene followed by the amount of 4-fluoroanisole (4FA) produced during the reaction. All solutions were heated at 140 °C for 15 minutes in sealed NMR tubes.