Water → Ethyl [4-(4,9-diethoxy-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate

HRID 15716

Reaktionsgleichung

Reaktionsgleichung von HRID 15716
[CH2:1]([O:3][C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7]([O:14][CH2:15][CH3:16])=[C:6]2[C:17]([O:19][C:20](=O)[C:5]=12)=[O:18])[CH3:2].[NH2:22][C:23]1[CH:28]=[CH:27][C:26]([CH2:29][C:30]([O:32][CH2:33][CH3:34])=[O:31])=[CH:25][CH:24]=1.O>C(O)(=O)C>[CH2:33]([O:32][C:30](=[O:31])[CH2:29][C:26]1[CH:25]=[CH:24][C:23]([N:22]2[C:20](=[O:19])[C:5]3[C:4]([O:3][CH2:1][CH3:2])=[C:13]4[CH:12]=[CH:11][CH:10]=[CH:9][C:8]4=[C:7]([O:14][CH2:15][CH3:16])[C:6]=3[C:17]2=[O:18])=[CH:28][CH:27]=1)[CH3:34]

Komponenten

5

Versuchsvorschrift

1,4-Diethoxy-2,3-naphthalenedicarboxylic anhydride (23.3 g, 81.5 mmol) and ethyl (4-aminophenyl)acetate (14.8 g, 82 mmol) were refluxed under nitrogen in acetic acid (160 ml) overnight. The mixture was cooled to room temperature and poured into water (1 L). The white solid was filtered, washed with water and dissolved in dichloromethane (800 ml). The solution was washed with water, brine and dried (MgSO4) and the solvent evaporated under vacuum to give ethyl[4-(4,9-diethoxy-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate as an off-white solid, 33 g, 96%.

Aufarbeitung

  1. filtrationThe white solid was filtered
  2. washwashed with water
  3. dissolutiondissolved in dichloromethane (800 ml)
  4. washThe solution was washed with water, brine
  5. dry with materialdried (MgSO4)
  6. customthe solvent evaporated under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-08ae92f127f94ec6a8ff8f48fe108716
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07732622B2

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