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Water → p-(3-Phthalimidopropoxy)acetophenone

HRID 1732485
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1732485
Br[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12](=[O:14])[CH3:13])=[CH:8][CH:7]=1.[C:15]1(=[O:25])[NH:19][C:18](=[O:20])[C:17]2=[CH:21][CH:22]=[CH:23][CH:24]=[C:16]12.[K].O>CN(C)C=O>[C:15]1(=[O:25])[N:19]([CH2:2][CH2:3][CH2:4][O:5][C:6]2[CH:11]=[CH:10][C:9]([C:12](=[O:14])[CH3:13])=[CH:8][CH:7]=2)[C:18](=[O:20])[C:17]2=[CH:21][CH:22]=[CH:23][CH:24]=[C:16]12
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 10061000HCID 10061000, VerbindungHCID 24194345Phthalimide potassium salt

Produkt 1

HCID 20306529p-(3-Phthalimidopropoxy)acetophenoneAusbeute 89 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

p-(3-Bromopropoxy)acetophenone (5.14 g.) and potassium phthalimide (3.75 g.) were dissolved in anhydrous N,N-dimethylformamide (50 ml.), and the solution was stirred at 70° C. for 2.5 hours. After the reaction mixture was allowed to cool, water (300 ml.) was poured thereto. The aqueous solution was extracted three times with ethyl acetate, and the extract was washed with ethyl acetate and then dried over magnesium sulfate. The ethyl acetate was removed by evaporation from the solution under reduced pressure, and the resultant residue was treated with ether to give p-(3-phthalimidopropoxy)acetophenone (5.75 g.).

Aufarbeitung

  1. temperatureto cool
  2. extractionThe aqueous solution was extracted three times with ethyl acetate
  3. washthe extract was washed with ethyl acetate
  4. dry with materialdried over magnesium sulfate
  5. customThe ethyl acetate was removed by evaporation from the solution under reduced pressure
  6. additionthe resultant residue was treated with ether

Quellen und Nachweise

ORD-Eintrag
ord-e8ec19c11ea14c5ba6aa433bde0f7a3d
Quelldatensatz
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04237305

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