Iodoethane → 1-(4-ethoxy-2-hydroxyphenyl)ethanone

Participants

Reaction Steps

Potassium carbonate (13.6 g, 99 mmol) followed by ethyl iodide (2.4 mL, 29.6 mmol) were added to a solution of 2′,4′-dihydroxyacetophenone (5 g, 33 mmol) in DMF (50 mL). The mixture was stirred for 4 hours and then partitioned between H2O and EtOAc. The organic layer was washed with satd NaHCO3, brine, dried over Na2SO4 and concentrated to a clear oil. Purification by column chromatography gave the product as a white solid (3.7 g, 63%). 1H NMR (400 MHz, CDCl3): δ 1.43 (t, J=6.8 Hz, 3H), 2.55 (s, 3H), 4.07 (d, J=7.1 Hz, 2H), 6.40 (s, 1H), 6.43 (d, J=8.8 Hz, 1H), 7.62 (d, J=8.8 Hz, 1H), 12.74 (s, 1H).

Provenance & Evidence