Molbank, Volume 2002, Issue 1

2-Bromo-4-methoxy-5-(1-methylethoxy)benzeneacetonitrile [1] (5.86 g, 20.6 mmol) was refluxed in 25% NaOH (50 mL)/EtOH (50 mL) for 12 h.[...]

2-Bromo-4-methoxy-5-(1-methylethoxy)benzeneacetic acid [1] (4.00 g, 13.2 mmol) and DMF (100 μL) were stirred in thionyl chloride (40 mL) for 3 h at ambient temperature.[...]

2-Bromo-4-methoxy-5-(1-methylethoxy)benzeneacetic acid chloride [1] (3.00 g, 9.33 mmol) was treated with dry EtOH (50 mL) at 0 °C.[...]

To a suspension of NaH (685 mg, 15.7 mmol, 55% in oil, purified by trituration with dry petroleum ether (3 x 30 mL)) in dry THF (30 mL) [[4-(1-methylethoxy)phenyl]methyl]propanedioic acid dimethyl ester [1] (4.00 g, 14.3 mmol) in dry THF (10 mL) was...

Compound 3 has been reported in a patent1 as a catalyst for hydrogen peroxide bleaching in photographic processing methods, but no synthesis or spectroscopic data are available in the chemical literature.[...]

Substituted pentanediones are widely used as ligands for metal complexes.[...]

To anhydrous AlCl3 (27.35 g, 205 mmol) and anisole (24.11 g, 223 mmol) in dry chloroform (300 mL) 2-bromobenzeneacetyl chloride [1] (43.4 g, 186 mmol) in dry chloroform (100 mL) was added over 30 min at 0 °C and stirred at ambient temperature for 15...

To 4-(2-bromoethyl)phenol [1] (28.75 g, 143 mmol) and tert-butyldimethylchlorosilane (23.64 g, 159 mmol) in dry THF (600 mL), imidazole (24.27 g, 357 mmol) was added at 15 °C over 10 min and stirred at ambient temperature.[...]

2-Bromo-5-hydroxy-4-methoxybenzenemethanol [1] (38.8 g, 166 mmol) in dry chloroform (200 mL) was treated with thionyl chloride (200 mL, 2.76 mol) at 0 °C and stirred for 3 h at ambient temperature.[...]

2-(3-Formylphenyl)imidazo[4,5-f][1,10]phenanthroline was prepared by a previously published method [1].[...]