反应详情

温度

0 °C

6-Ethyl-4-hydroxy-3-propionyl-2-H-pyran-2-one (III in Scheme 1; Example 1.2; 0.5 g; 2.56 mmol) was dissolved in 20 ml anhydrous THF and cooled to 0° C. under argon. To the cooled solution, was added LDA (5.12 ml of 1.5 M solution in cyclohexane; 7.68 mmol; Aldrich) and the reaction mixture was stirred for 30 min. To the cooled reaction mixture, was added 3-bromopropoxy-t-butyldimethylsilane (0.77 g; 3.07 mmol; Aldrich) and 1 ml HMPA (Aldrich). The reaction mixture was stirred for 30 min at 0° C., quenched with saturated NH4Cl, extracted with 3×20 ml EtOAc, dried with anhydrous Na2SO4, and evaporated to an oil. The product was purified via silica chromatography (10% EtOAc in hexanes).

1. customTo the cooled reaction mixture
2. stirringThe reaction mixture was stirred for 30 min at 0° C.
3. customquenched with saturated NH4Cl
4. extractionextracted with 3×20 ml EtOAc
5. dry with materialdried with anhydrous Na2SO4
6. customevaporated to an oil
7. customThe product was purified via silica chromatography (10% EtOAc in hexanes)