反应详情

Following the method described in Example 4, a solution of 3.2 g of 1,4-dimethoxy-3-bromo-naphthalene in anhydrous tetrahydrofuran was treated at -78° C. with n-butyllithium and then added to a solution in anhydrous tetrahydrofuran of 2.7 g of the compound prepared in Example 3. After silica gel column purification 2.8 g of the title compound was obtained (65% yield) m/z 426 (M+.): IR (film): 1780 cm-1 (C=O, five membered ring lactone), 1670 cm-1 (C=O, benzylic ketone); PMR (CDCl3): inter alia: δ 1.4 (s, CH3), 3.85 (s, two OCH3), 3.9 (s, --O--CH2 --CH2 --O--), 6.9 (s, aromatic H) and 7.4-8.4 (m, four aromatic H).

1. customAfter silica gel column purification 2.8 g of the title compound
2. customwas obtained (65% yield) m/z 426 (M+.)