StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Acetic Acid → N-(2-Amino-4-bromophenyl)-2-chloroacetamide

HRID 44186
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 44186
[Cl-].[NH4+].C(O)(=O)C.[Br:7][C:8]1[CH:13]=[CH:12][C:11]([NH:14][C:15](=[O:18])[CH2:16][Cl:17])=[C:10]([N+:19]([O-])=O)[CH:9]=1.C(=O)([O-])[O-].[Na+].[Na+]>O.CN(C=O)C>[NH2:19][C:10]1[CH:9]=[C:8]([Br:7])[CH:13]=[CH:12][C:11]=1[NH:14][C:15](=[O:18])[CH2:16][Cl:17]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 176Acetic AcidHCID 10340Sodium CarbonateHCID 25517Ammonium ChlorideHCID 16457083N-(4-bromo-2-nitrophenyl)-2-chloroacetamide

Produkt 1

HCID 66911433N-(2-Amino-4-bromophenyl)-2-chloroacetamideAusbeute 43,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962
Water
Lösungsmittel
HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

Ferrous powder (19.8 g, 354 mmol), ammonium chloride (1.1 g, 19.7 mmol) and acetic acid (4.9 ml, 86.5 mmol) were suspended in 300 ml water and stirred at 50° C. for 15 min. To this mixture, a solution of N-(4-bromo-2-nitrophenyl)-2-chloroacetamide (11.5 g, 39.3 mmol) in 100 ml DMF was added quickly. After stirring for 15 min, the mixture was basified to pH 9 with aqueous sodium carbonate solution. The remaining solids were filtered and washed with water and ethyl acetate. Extraction of the water layer with ethyl acetate, washing of the combined organic layers with brine, drying over MgSO4, removing the solvent under reduced pressure and purification of the crude product by flash chromatography on silica gel (petroleum ether/ethyl acetate, 1/1) yielded N-(2-amino-4-bromophenyl)-2-chloroacetamide (4.5 g, 17.0 mmol, 43%) as an off-white solid.

Aufarbeitung

  1. stirringAfter stirring for 15 min
  2. filtrationThe remaining solids were filtered
  3. washwashed with water and ethyl acetate
  4. extractionExtraction of the water layer with ethyl acetate
  5. washwashing of the combined organic layers with brine
  6. dry with materialdrying over MgSO4
  7. customremoving the solvent
  8. customunder reduced pressure and purification of the crude product by flash chromatography on silica gel (petroleum ether/ethyl acetate, 1/1)

Quellen und Nachweise

ORD-Eintrag
ord-43f833b971914c87909b782e12612778
Quelldatensatz
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08541404B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion