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

Acetic Acid → 4-bromo-2-fluoro-N,N-dimethylaniline

HRID 1960119
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1960119
[F:1][C:2]1[CH:8]=[C:7]([Br:9])[CH:6]=[CH:5][C:3]=1N.[BH3-][C:11]#[N:12].[Na+].O.[OH-].[K+].[CH3:17]C(O)=O>>[Br:9][C:7]1[CH:6]=[CH:5][C:3]([N:12]([CH3:11])[CH3:17])=[C:2]([F:1])[CH:8]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 5

HCID 176Acetic AcidHCID 962WaterHCID 14797Potassium HydroxideHCID 1230504-Bromo-2-fluoroanilineHCID 5003444Sodium cyanoborohydride

Produkt 1

HCID 404253644-bromo-2-fluoro-N,N-dimethylaniline

Versuchsvorschrift

To a solution of 2-fluoro-4-bromoaniline (1.0 g, 5.26 mmol) in AcOH (20 mL) at rt was added NaCNBH3 (1.654 g, 26.3 mmol). The mixture was stirred at rt overnight (˜17 h). The reaction was cooled in an ice bath. Water (10 mL) was added, followed by solid KOH until pH >11. The mixture was extracted with DCM. The combined extracts were dried (MgSO4) and concentrated to afford the title compound, which was used without further purification. LC-MS: calculated for C8H9BrFN 218.07, observed m/e 219.99 (M+H)+ (Rt 0.96 min).

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Aufarbeitung

  1. temperatureThe reaction was cooled in an ice bath
  2. extractionThe mixture was extracted with DCM
  3. dry with materialThe combined extracts were dried (MgSO4)
  4. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-eccc44e863474448a23bf9e079a3e973
Quelldatensatz
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08410284B2

Notizen zur Reaktion

Wird geladen…