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Water → 2-Bromo-N-methyl-N-phenylacetamide

HRID 2192364
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2192364
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(=O)([O-])[O-].[K+].[K+].[Br:15][CH2:16][C:17](Br)=[O:18].O>ClCCl>[Br:15][CH2:16][C:17]([N:2]([CH3:1])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1)=[O:18]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 7515N-MethylanilineHCID 11430Potassium CarbonateHCID 61147Bromoacetyl bromide

Produkt 1

HCID 344952-Bromo-N-methyl-N-phenylacetamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a mixture of N-methyl aniline (5 mL) and potassium carbonate (9.6 g) in 100 mL dichloromethane was added bromoacetyl bromide (8.1 mL) (exotherm). The mixture was stirred for 4.5h then water was added. The phases were separated and the organic layer was concentrated. The crude product was purified by silica gel chromatography eluting with 0-100% EtOAc/cyclohexane. The relevant fractions were combined and evaporated and the residue was taken up in dichloromethane and washed with water. The organic layer was stirred with another portion of water for a few minutes and then the layers were separated. Evaporation of the organic layer gave the sub-titled compound (10.2 g) as a straw coloured solid.

Aufarbeitung

  1. customThe phases were separated
  2. concentrationthe organic layer was concentrated
  3. customThe crude product was purified by silica gel chromatography
  4. washeluting with 0-100% EtOAc/cyclohexane
  5. customevaporated
  6. washwashed with water
  7. customthe layers were separated
  8. customEvaporation of the organic layer

Quellen und Nachweise

ORD-Eintrag
ord-5872088bc0a441e9ad9dacb7f454debf
Quelldatensatz
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08329729B2

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