Réaction #577224

ord-b6acc544959042bb8b7325ba902fd268

Équation de réaction

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
Rendement 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
Rendement 62.0%

Solvants

Conditions de réaction

Température
90°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    ConcentrationThe mixture was concentrated
  2. 2
    workup.ADDITIONdiluted with ethyl acetate
  3. 3
    Lavagewashed with 10% NaHCO3, brine
  4. 4
    Séchagedried with anhydrous Na2SO4
  5. 5
    Autreevaporated
  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
    Concentrationconcentrated
  9. 9
    AutreThe residue was purified by column chromatography (ethyl acetate/hexane=1:1)

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07527934B2uspto-grants-2009_05