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

Acetone → 5-Bromo-3-fluorobenzene-1,2-diamine

HRID 408698
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 408698
[Br:1][C:2]1[CH:3]=[C:4]([F:12])[C:5]([N+:9]([O-])=O)=[C:6]([NH2:8])[CH:7]=1.[NH4+].[Cl-].CC(C)=O>[Zn].O>[Br:1][C:2]1[CH:7]=[C:6]([NH2:8])[C:5]([NH2:9])=[C:4]([F:12])[CH:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 180AcetoneHCID 25517Ammonium ChlorideHCID 669372325-Bromo-3-fluoro-2-nitroaniline

Produkt 1

HCID 27732795-Bromo-3-fluorobenzene-1,2-diamine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23994ZincKatalysatorHCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
23 °C

Versuchsvorschrift

To a solution of 5-bromo-3-fluoro-2-nitro-phenylamine (2 g, 8.5 mmol), NH4Cl (6.81 g, 127.6 mmol), acetone (100 mL) and water (20 mL), was added zinc powder portion-wise (three equal portions over 5 minutes) (8.34 g, 127.6 mmol) at 0° C. The mixture was stirred for 2 h then warmed to 23° C. The mixture was filtered through Celite® and the solvents were concentrated under reduced pressure. The mixture was re-dissolved in EtOAc/DCM and filtered a second time through Celite® and the solvents were evaporated. The crude mixture was diluted with EtOAc (200 mL), washed with brine (40 mL), dried, filtered, and concentrated under reduced pressure. The resultant residue was used in the next reaction without further purification.

Aufarbeitung

  1. filtrationThe mixture was filtered through Celite®
  2. concentrationthe solvents were concentrated under reduced pressure
  3. dissolutionThe mixture was re-dissolved in EtOAc/DCM
  4. filtrationfiltered a second time through Celite®
  5. customthe solvents were evaporated
  6. additionThe crude mixture was diluted with EtOAc (200 mL)
  7. washwashed with brine (40 mL)
  8. customdried
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. customThe resultant residue was used in the next reaction without further purification

Quellen und Nachweise

ORD-Eintrag
ord-d89cf31e572949aaab12efec56e135eb
Quelldatensatz
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08759345B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion