Reacción #577224
ord-b6acc544959042bb8b7325ba902fd268
Ecuación de reacción
Reactantes
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1ConcentraciónThe mixture was concentrated
- 2workup.ADDITIONdiluted with ethyl acetate
- 3Lavadowashed with 10% NaHCO3, brine
- 4Secadodried with anhydrous Na2SO4
- 5Otroevaporated
- 6workup.DISSOLUTIONThe residue was dissolved in dry DCM (25 mL)
- 7workup.STIRRINGThe mixture was stirred for 2 h at room temperature
- 8Concentraciónconcentrated
- 9OtroThe residue was purified by column chromatography (ethyl acetate/hexane=1:1)
Procedimiento
Methyl bromoacetate (0.25 mL, 2.65 mmol) was added dropwise to a stirred mixture of 21 (0.33 g, 0.89 mmol) and K2CO3 (0.36 g, 2.65 mmol) in dry DMF (20 mL) under argon. The resulting mixture was stirred for 4 h at 90° C. The mixture was concentrated, diluted with ethyl acetate, washed with 10% NaHCO3, brine, dried with anhydrous Na2SO4, and evaporated. The residue was dissolved in dry DCM (25 mL). Tetrakis(triphenylphosphine) palladium(0) (58 mg, 0.05 mmol) and phenylsilane (1.1 mL, 8.90 mmol) were added. The mixture was stirred for 2 h at room temperature and concentrated. The residue was purified by column chromatography (ethyl acetate/hexane=1:1) to give 22 as a yellow solid (0.22 g, 62%). TLC (ethyl acetate/hexane, 3:1): Rf=0.5. mp 236° C. 1H NMR (CDCl3/CD3OD, 500 MHz) δ 3.76 (s, 3H, CO2CH3), 4.69 (s, 2H, CH2), 6.68 (m, 6H), 7.19 (d, J=7.5 Hz, 1H), 7.66 (t, J=7.5 Hz, 1H), 7.71 (t, J=7.5 Hz, 1H), 8.01 (d, J=7.5 Hz, 1H). 13C NMR (CDCl3/CD3OD, 125 MHz) δ 52.33, 65.18, 101.86, 102.77, 109.84, 111.55, 112.37, 112.52, 124.05, 124.87, 126.67, 129.00, 129.24, 129.80, 135.21, 152.47, 152.56, 152.94, 159.34, 169.21, 170.15, 171.36, 172.03. ESIMS calcd for C23H17O7 [M+H]+ 405.1. Found 405.2.