反应详情

The title compound was prepared according to the procedure in Example 4 using 4-(2-butyl-benzofuran-3-ylmethyl)-phenol (0.500 g, 1.78 mmol) and 4-chlorosulphonyl-2-hydroxybenzoic acid (0.844 g, 3.56 mmol). Purification on 2% H3PO4 /MeOH treated silica gel, eluting with EtOAc/hexane gave 0.728 g (86%) of the title compound as an orange solid, mp 135-138° C. 1H NMR (DMSO-d6) δ 0.84 (t, 3 H), 1.27 (sextet, 2 H), 1.58 (quintet, 2 H), 2.76 (t, 2 H), 3.97 (s, 2 H), 6.96 (d, 2 H), 7.10 (dt, 1 H), 7.17 (dt, 1 H), 7.22-7.31 (m, 5 H), 7.43 (d, 1 H), 7.95 (d, 1 H). IR (KBr) 3300, 2950, 1675, 1390 and 1175 cm-1. mass spectrum (-ESI) m/z 479 (M-H). Anal. Calcd. for C26H24O7S.0.2H2O: C, 64.50; H, 5.08; N, 0.00. Found: C, 64.50; H, 5.07; n, 0.06.

1. customThe title compound was prepared
2. customPurification on 2% H3PO4 /MeOH
3. additiontreated silica gel
4. washeluting with EtOAc/hexane