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. Author manuscript; available in PMC: 2011 Jul 28.
Published in final edited form as: J Am Chem Soc. 2010 Jul 28;132(29):9990–9991. doi: 10.1021/ja1044874

Table 4.

One-Pot Synthesis of Benzofuransa

graphic file with name nihms220226u4.jpg
Entry Substrate Ketone Product Yield [%] Time [h]
1 graphic file with name nihms220226t1.jpg graphic file with name nihms220226t2.jpg graphic file with name nihms220226t3.jpg 86% 1
2 graphic file with name nihms220226t4.jpg graphic file with name nihms220226t5.jpg graphic file with name nihms220226t6.jpg 68% 1
3 graphic file with name nihms220226t7.jpg graphic file with name nihms220226t8.jpg graphic file with name nihms220226t9.jpg 88% 1
4 graphic file with name nihms220226t10.jpg graphic file with name nihms220226t11.jpg graphic file with name nihms220226t12.jpg 83% 2
5 graphic file with name nihms220226t13.jpg graphic file with name nihms220226t14.jpg graphic file with name nihms220226t15.jpg 68% 2
6 graphic file with name nihms220226t16.jpg graphic file with name nihms220226t17.jpg graphic file with name nihms220226t18.jpg 55% 2
a

Oxime (1 equiv), ketone (2 equiv), H2O (5 equiv), HCl (4 M in dioxane, 5 equiv), 1,4-dioxane (0.2 M), 70 °C, 1–2 h; isolated yield, average of 2 runs on a 0.5 – 1.0 mmol scale.