Bromine → N-(2-Bromophenyl)-2,2,2-trifluoroacetamide

Temperatur

25 °C

To a stirred mixture of the N-trifluoroacetylaniline (2.00 mmol) and sodium hydrogen carbonate (0.21 g, 2.50 mmol, 1.25 eq) in methanol (10 mL) at 0° C. is added dropwise bromine (0.113 mL, 2.19 mmol, 1.1 eq). The resulting reaction mixture is then stirred at 25° C. for 30 minutes. The reaction mixture is then evaporated under reduced pressure, and the residue is placed in water made acidic to pH 3 with HCl (10 mL). This aqueous mixture is extracted with ethyl acetate (3×15 mL). The extracts is combined, dried (MgSO4), and evaporated under reduced pressure. The residue is column chromatographed using silica gel (approximately 50 g) and elution with an appropriate solvent system to afford the corresponding 2-bromo-N-trifluoroacetylaniline.

1. customThe resulting reaction mixture
2. customThe reaction mixture is then evaporated under reduced pressure
3. extractionThis aqueous mixture is extracted with ethyl acetate (3×15 mL)
4. dry with materialdried (MgSO4)
5. customevaporated under reduced pressure
6. customchromatographed
7. washsilica gel (approximately 50 g) and elution with an appropriate solvent system

ORD-Eintrag

ord-54c7d2970c01459db69074daf15ff12e

Quelldatensatz

uspto-grants-2002_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06380233B1