反应详情

Orcinol monohydrate (1.42 g, 10 mmol) and 2-chlorobenzenesulfonyl chloride (2.43 g, 11 mmol) were mixed in saturated NaHCO3 (30 mL) and diethyl ether (30 mL). The biphasic mixture was stirred vigorously at room temperature for 2 days. The reaction mixture was quenched with 50 mL of water and extracted into ethyl acetate (3×50 mL). The organic phase was washed with brine (2×50 mL) and dried over Na2SO4. After removing the solvent in vacuo, the residue was purified by flash column chromatography (2% ethyl acetate in methylene chloride) to give the title compound as a pale-yellow liquid (2.15 g, 71%). 1H-NMR (300 MHz, CDCl3) δ 2.22 (s, 3 H), 5.24 (s, 1 H), 6.43 (s, 1 H), 6.52 (s, 2H), 7.38 (m, 1 H), 7.60 (m, 2 H), and 7.96 (dd, 1 H, J=0.6, 3.9 Hz).

1. customThe reaction mixture was quenched with 50 mL of water
2. extractionextracted into ethyl acetate (3×50 mL)
3. washThe organic phase was washed with brine (2×50 mL)
4. dry with materialdried over Na2SO4
5. customAfter removing the solvent in vacuo
6. customthe residue was purified by flash column chromatography (2% ethyl acetate in methylene chloride)