反应详情

The title compound was prepared as described in General Method 6 from 0.96 mmol of 3-bromo-5,6-dihydro-4-hydroxy-6,6-diphenyl-2H-pyran-2-one (prepared in example AAA), 1.0 mmol of benzenethiol, and 1.0 mmol of piperidine in 20 mL of dichloromethane. The product was triturated with hexane:ether (1:1) to afford a solid (m.p. 78°-80° C.). 1H NMR (DMSO-d6) δ3.37 (bs, 2H), 6.35 (m, 2H), 6.93 (m, 3H), 7.29-7.49 (m, 10H).

1. customThe product was triturated with hexane:ether (1:1)