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. 2019 Aug 9;58(37):13149–13154. doi: 10.1002/anie.201907488

Table 2.

Optimization of the 18F‐difluoromethylation reaction. Inline graphic

Entry

Deviation from standard reaction conditions

RCY [18F]5 [%]

(of the crude reaction mixture)

1

benzophenone[a]

47±5

2

Ru(bpy)3 (0.01 μmol)

0

3

70±7

4

After HPLC purification of [18F]5

42±4[b]

5

55 °C

51±10

6

30 s

60±8

7

Ir(ppy)3 (0.001 μmol)

42±2

8

DMF

44±1

9

DMSO/H2O (200/50 μL)

45±10

10

no catalyst

0

11

no light

0

12

TEMPO

0

[a] Benzophenone (10 μmol), 365 nm, [b] Radiochemical yield (n=4) of isolated product.