Reacción #1106683

ord-5627724ec484411ca80cf9c75b5d5d97

Ecuación de reacción

Oc1ccccc1O
Catechol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1ccc(S(=O)(=O)OC[C@H]2CO2)cc1
(2R)-glycidyl tosylate
OC[C@H]1COc2ccccc2O1
((2S)-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methanol

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction was cooled to room temperature
  2. 2
    Extracciónextracted with diethyl ether (4 times)
  3. 3
    LavadoThe combined organic solution was washed 3 times with 10% potassium carbonate
  4. 4
    Otroonce with water, once with brine and evaporated in vacuo
  5. 5
    Otroto yield a white solid which
  6. 6
    Otrowas purified by flash column chromatography (DCM:Methanol—50:1)

Procedimiento

Catechol (13.2 g, 0.12 mol) and potassium carbonate (16.6 g, 0.12 mol) were stirred in DMF (250 mL) and (2R)-glycidyl tosylate (22.8 g, 0.10 mol) was added and the reaction was stirred at 60° C. for 24 h. The reaction was cooled to room temperature and diluted with ice water (1 L) and extracted with diethyl ether (4 times). The combined organic solution was washed 3 times with 10% potassium carbonate, once with water, once with brine and evaporated in vacuo to yield a white solid which was purified by flash column chromatography (DCM:Methanol—50:1) to yield ((2S)-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methanol as a solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08716231B2uspto-grants-2014_05