Reacción #338967

ord-c0559f0ff65d4f29bdb383e3ad7971d8

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGstirring
  2. 2
    workup.WAITcontinued for another 24 hours
  3. 3
    Lavadowas then washed with a 2% sodium hydroxide (w/w) solution until no p-nitrophenol
  4. 4
    SecadoThe dichloromethane was dried with sodium sulfate
  5. 5
    Filtraciónfiltered
  6. 6
    Otroevaporated under reduced pressure

Procedimiento

To a stirring slurry of 9-anthracenemethanol (10 g, 48 mmol) and 4-nitrophenyl chloroformate (13.6 g, 67.5 mmol) in 200 ml CH2Cl2 was added triethylamine (6.7 ml, 0.19 mol). The resulting gold colored solution was allowed to stir 16 hrs at room temperature. At this point, 2-(2-aminoethoxy)ethanol (14.4 ml, 0.144 mol) was added and stirring continued for another 24 hours. The CH2Cl2 reaction mixture was then washed with a 2% sodium hydroxide (w/w) solution until no p-nitrophenol was observed in the organic layer. The dichloromethane was dried with sodium sulfate, filtered, and evaporated under reduced pressure.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07867726B2uspto-grants-2011_01