反应详情

1-(3,4-Dimethoxyphenyl)-1-(3-ethoxy-4-methoxyphenyl)but-1-ene was prepared analogously to methyl 3,3-bis-(3,4-dimethoxyphenyl)acrylate using 3,4-dimethoxy-3'-ethoxy-4'-methoxybenzophenone (1 g, 3.2 mmol), propyltriphenylphosphonium bromide (1.34 g, 3.5 mmol) and lithium hexamethyldisilazide (2.7 mL, 3.5 mmol, 1.3M) with a reaction time of 2.5 hours at room temperature. The crude mixture was purified by chromatography (silica gel, methylene chloride) followed by a Kugelrohr distillation to yield 0.77 g (71%) of a mixture of the E and Z isomers as an oil: 1H NMR (CDCl3) δ 6.92-6.65 (m, 12H), 6.02-5.89 (m, 2H), 4.12-3.96 (m, 4H), 3.92 (s, 3H), 3.86 (s, 3H), 3.85 (s, 3H), 3.82 (s, 3H), 3.81 (s, 3H), 2.22-2.04 (m, 4H), 1.51-1.38 (m, 6H), 1.14-0.98 (m, 6H); 13C NMR (CDCl3) δ 148.5, 148.1, 147.8, 147.7, 140.4, 140.4, 136.0, 135.9, 133.0, 132.9, 130.1, 130.0, 122.2, 119.8, 114.6, 113.1, 112.0, 111.0, 110.7, 110.4, 64.3, 64.2, 55.9, 23.2, 14.8, 14.7; Anal. Calcd for C21H26O4. Theoretical: C, 73.66; H, 7.65. Found: C, 73.32; H, 7.26.

1. customwith a reaction time of 2.5 hours
2. customat room temperature
3. customThe crude mixture was purified by chromatography (silica gel, methylene chloride)
4. distillationfollowed by a Kugelrohr distillation