Reacción #577224

ord-b6acc544959042bb8b7325ba902fd268

Ecuación de reacción

COC(=O)CBr
Methyl bromoacetate
C=CCOC(=O)c1ccccc1-c1c2ccc(=O)cc-2oc2cc(O)ccc12
21
C=CCOC(=O)c1ccccc1-c1c2ccc(=O)cc-2oc2cc(O)ccc12
2-(6-Hydroxy-3-oxo-3H-xanthen-9-yl)-benzoic acid 2-propenyl ester
O=C([O-])[O-].[K+].[K+]
K2CO3
[SiH3]c1ccccc1
phenylsilane
COC(=O)COc1ccc2c(c1)Oc1cc(O)ccc1C21OC(=O)c2ccccc21
22
Rendimiento 62.0%
COC(=O)COc1ccc2c(c1)Oc1cc(O)ccc1C21OC(=O)c2ccccc21
(6′-hydroxy-3-oxospiro[isobenzofuran-1(3H), 9′-[9H]xanthen]-3′-yl)oxy-acetic acid methyl ester
Rendimiento 62.0%

Disolventes

Condiciones de reacción

Temperatura
90°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe mixture was concentrated
  2. 2
    workup.ADDITIONdiluted with ethyl acetate
  3. 3
    Lavadowashed with 10% NaHCO3, brine
  4. 4
    Secadodried with anhydrous Na2SO4
  5. 5
    Otroevaporated
  6. 6
    workup.DISSOLUTIONThe residue was dissolved in dry DCM (25 mL)
  7. 7
    workup.STIRRINGThe mixture was stirred for 2 h at room temperature
  8. 8
    Concentraciónconcentrated
  9. 9
    OtroThe 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07527934B2uspto-grants-2009_05