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

HRID 1945280
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1945280
[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).

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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-d5c81efe9db6403cba08fc9a73728ba9
Quelldatensatz
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08394969B2

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