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. Author manuscript; available in PMC: 2017 Aug 5.
Published in final edited form as: Org Lett. 2016 Jul 14;18(15):3910–3913. doi: 10.1021/acs.orglett.6b01952

Table 2.

Direct Arylation of Tritylanilinesa

graphic file with name nihms814656u3.jpg

entry substrate product yield, %
1 graphic file with name nihms814656t19.jpg graphic file with name nihms814656t20.jpg 93
2 graphic file with name nihms814656t21.jpg graphic file with name nihms814656t22.jpg 82
3 graphic file with name nihms814656t23.jpg graphic file with name nihms814656t24.jpg 61
4 graphic file with name nihms814656t25.jpg graphic file with name nihms814656t26.jpg 62
5 graphic file with name nihms814656t27.jpg graphic file with name nihms814656t28.jpg 96
a

4-Methoxy-N-tritylaniline (0.2 mmol), silyl aryl bromide or iodide (0.36 mmol), CsF (0.75 mmol), solvent (2.5 mL), 110 °C, 48 h; then TFA (1.5 mL). Yields are isolated yields. See the Supporting Information for details. TFA = CF3CO2H; DME = 1,2-dimethoxyethane.