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Hydrochloric Acid → 2-(Methyl-3-nitro-benzyl)-isoindole-1,3-dione

HRID 1454288
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1454288
C[C:2]1[CH:13]=[CH:12][C:5]([CH2:6]OS(C)(=O)=O)=[CH:4][C:3]=1[N+:14]([O-:16])=[O:15].[CH3:17]N(C=O)C.[C:22]1(=[O:32])[NH:26][C:25](=[O:27])[C:24]2=[CH:28][CH:29]=[CH:30][CH:31]=[C:23]12.[K].Cl>CCCCCC.C(OCC)(=O)C>[CH3:17][CH:6]([N:26]1[C:22](=[O:32])[C:23]2[C:24](=[CH:28][CH:29]=[CH:30][CH:31]=2)[C:25]1=[O:27])[C:5]1[CH:12]=[CH:13][CH:2]=[C:3]([N+:14]([O-:16])=[O:15])[CH:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 6228DimethylformamideHCID 208002884-Methyl-3-nitrobenzyl methanesulfonateHCID 24194345Phthalimide potassium salt

Produkt 1

HCID 223935242-(Methyl-3-nitro-benzyl)-isoindole-1,3-dione

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 21226206
Ethyl acetate hexane
Lösungsmittel

Versuchsvorschrift

Methanesulfonic acid 4-methyl-3-nitro-benzyl ester (0.45 g, 1.83 mmol) was added to anhydrous DMF (20 mL), under argon, and potassium phthalimide (0.34 g, 1.83 mmol) was added. The reaction mixture was heated to 60EC for 12 h. The reaction mixture was cooled and poured into 1N HCl and the aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with water, brine and dried over anhydrous magnesium sulfate. The solution was filtered and the solvent removed under reduced pressure. The product was isolated by flash chromatography. (4:1 hexane/ethyl acetate) Yield 0.45 g. 1H NMR (CDCl3, 300 MHz): δ 2.58 (s, 3H), 4.88 (s, 2H), 7.30 (d, J=7 Hz, 1H), 7.57 (d, J=7 Hz, 1H), 7.24-7.77 (m, 2H), 7.84-7.89 (m, 2H), 8.02 (s, 1H).

Aufarbeitung

  1. temperatureThe reaction mixture was heated to 60EC for 12 h
  2. temperatureThe reaction mixture was cooled
  3. extractionthe aqueous layer was extracted three times with ethyl acetate
  4. washThe combined organic layers were washed with water, brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationThe solution was filtered
  7. customthe solvent removed under reduced pressure
  8. customThe product was isolated by flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-a802a2e2bf08422f94821e94216eb39c
Quelldatensatz
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07479495B2

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