Boron tribromide → 5-(4-Hydroxy-2-methyl-phenyl)-4-methyl-thiophene-2-carboxylic acid methyl ester

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Reaction Steps

To a 0° C. solution of 5-(4-methoxy-2-methyl-phenyl)-4-methyl-thiophene-2-carboxylic acid methyl ester (540 mg, 2 mmol) in dichloromethane (30 mL) is added BBr3 in dichloromethane (1N, 5.0 mL) and the mixture is stirred at ambient temperature overnight. The reaction is quenched by addition of methanol and evaporated. The residue is purified by column chromatography on silica gel eluting with 0-20% EtOAc in hexanes to give the title compound (420 mg, 82%). 1H NMR (CDCl3): δ 7.62 (s, 1H), 7.10 (d, 1H, J=7.9 Hz), 6.76 (s, 1H), 6.70 (d, 1H, J=7.9 Hz), 4.79 (bs, 1H), 3.88 (s, 3H), 2.15 (s, 3H), 2.02 (s, 3H).

Provenance & Evidence