Methyl acetoacetate → 5,6-Dihydro-6-phenyl-6-(2-phenylethyl)-2H-pyran-2-one

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The title compound was prepared as described in General Method 1 using 25 mmol of methyl acetoacetate, 27.5 mmol of NaH 60% dispersion in oil, 26.25 mmol of 1.6M n-butyl lithium in hexane, 25 mmol of 3-phenylpropiophenone and 70 mL of tetrahydrofuran. Upon concentrating the reaction a solid precipitated out which was triturated with ether and filtered (m.p. 130-130.55, °C.). 1H NMR (CDCl3) δ2.2-2.4 (m, 2H), 2.4-2.6 (m, 1H), 2.6-2.8 (m, 1H), 2.9 (d, 1H), 3.0 (d, 1H), 3.3 (d, 1H), 3.4 (d, 1H), 7.0-7.5 (m, 15H).

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