Reaktion #2006442

ord-847a1d33b4cf43d084f625e651ea099f

Reaktionsgleichung

NCCOCCO
2-(2-aminoethoxy)ethanol
OCc1c2ccccc2cc2ccccc12
9-anthracenemethanol
O=C(Cl)Oc1ccc([N+](=O)[O-])cc1
4-nitrophenyl chloroformate
CCN(CC)CC
triethylamine
O=C(NCCOCCO)OCc1c2ccccc2cc2ccccc12
[2-(2-Hydroxy-ethoxy)-ethyl]-carbamic acid anthracen-9-ylmethyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08168405B2uspto-grants-2012_05