Potassium Carbonate → Oxirane, 2-methyl-3-phenyl-, cis-

Temperature

-10 °C

To a solution of cis-β-methyl styrene (0.059 g, 0.5 mmol) and ketone IVd (0.026 g, 0.075 mmol) in DME-DMM (3:1, v/v) (7.5 mL) were added buffer (0.2 M K2CO3—AcOH in 4×10−4 M aqueous EDTA, buffer pH=8.0) (5 mL) and Bu4NHSO4 (0.0075 g, 0.02 mmol) with stirring. After the mixture was cooled to about −10° C. (bath temperature) via a NaCl-ice bath, a solution of Oxone® (0.212 M in 4×10−4 M aqueous EDTA, 4.2 mL) (0.548 g, 0.89 mmol) and K2CO3 (0.479 M in 4×10−4 M aqueous EDTA, 4.2 mL) (0.278 g, 2.01 mmol) were added dropwise separately over a period of 3.5 h via a syringe pump. The reaction was then quenched with the addition of pentane and extracted with pentane. The combined organic layers were washed with brine, dried (Na2SO4), filtered, concentrated, and purified by flash chromatography (the silica gel was buffered with 1% Et3N in pentane; pentane-ether (1/0 to 50/1 was used as eluent) to give cis-β-methylstyrene oxide as a colorless liquid (0.58 g, 87% yield, 91% ee).

1. customThe reaction was then quenched with the addition of pentane
2. extractionextracted with pentane
3. washThe combined organic layers were washed with brine
4. dry with materialdried (Na2SO4)
5. filtrationfiltered
6. concentrationconcentrated
7. custompurified by flash chromatography (the silica gel

ORD record

ord-f838a3b6a1244e14aca52dc4585ca891

Source dataset

uspto-grants-2006_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07153971B2