Ethanol → Ethyl 2-nitro-5-phenoxybenzoate

HRID 2099972Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2099972
[N+:1]([C:4]1[CH:12]=[CH:11][C:10]([O:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:9][C:5]=1[C:6]([OH:8])=[O:7])([O-:3])=[O:2].OS(O)(=O)=O.C([O-])(O)=O.[Na+].[CH3:30][CH2:31]O>>[N+:1]([C:4]1[CH:12]=[CH:11][C:10]([O:13][C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)=[CH:9][C:5]=1[C:6]([O:8][CH2:30][CH3:31])=[O:7])([O-:3])=[O:2]

Komponenten

5

Versuchsvorschrift

A solution of 34A (4.5 g, 17.4 mmol) in EtOH (120 mL) was treated with concentrated H2SO4 (4 mL) and heated to reflux for 24 hours. The mixture was cooled to room temperature and neutralized with 5% NaHCO3. The resulting solution was extracted with CH2Cl2, dried (MgSO4), filtered, and concentrated to afford 43A (2.6 g, 65%).

Aufarbeitung

  1. temperatureheated
  2. temperatureto reflux for 24 hours
  3. extractionThe resulting solution was extracted with CH2Cl2
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-c9f970aa0c594391b9456f0417f654a3
Quelldatensatz
uspto-grants-2009_08
Patentnummer
US07569725B2

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