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1,3-Benzodioxol-5-amine, N-ethyl- → N-1,3-Benzodioxol-5-yl-N-ethylurea

HRID 1884357
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1884357
[CH2:1]([NH:3][C:4]1[CH:9]=[CH:8][C:7]2[O:10][CH2:11][O:12][C:6]=2[CH:5]=1)[CH3:2].[O:13]([C:15]#[N:16])[Na]>CC(O)=O>[CH2:1]([N:3]([C:4]1[CH:9]=[CH:8][C:7]2[O:10][CH2:11][O:12][C:6]=2[CH:5]=1)[C:15]([NH2:16])=[O:13])[CH3:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 1183651,3-Benzodioxol-5-amine, N-ethyl-HCID 178418852HCID 178418852, Verbindung

Produkt 1

HCID 13098802N-1,3-Benzodioxol-5-yl-N-ethylureaAusbeute 59,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

To a solution of N-ethyl-3,4-(methylenedioxy)aniline (8.1 g) in AcOH (100 mL) was added NaOCN (3.0 g) at 10° C. The cold bath was removed and the mixture was stirred at rt for 24 h. The solvent was removed in vacuo and the resulting residue was neutralized with 2 N NaOH. The mixture was extracted with chloroform (3×50 mL). The combined organic phase was washed with water and brine, dried over Na2SO4. The solvent was removed in vacuo and the resulting residue was recrystallized from chloroform/hexane to yield the title compound (5.7 g, 56%). 1NMR (CDCl3): 6.78-6.72 (m, 3H), 6.02 (s, 2H), 4.38 (br s, 2H), 3.66 (q, J=7.0, 2H), 1.11 (t, J=7.0, 3H).

Aufarbeitung

  1. customThe cold bath was removed
  2. customThe solvent was removed in vacuo
  3. extractionThe mixture was extracted with chloroform (3×50 mL)
  4. washThe combined organic phase was washed with water and brine
  5. dry with materialdried over Na2SO4
  6. customThe solvent was removed in vacuo
  7. customthe resulting residue was recrystallized from chloroform/hexane

Quellen und Nachweise

ORD-Eintrag
ord-1ed9822a53224ceea266fd6bf3261b82
Quelldatensatz
uspto-grants-2004_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06765006B2

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