Acetyl chloride → 4'-Bromoacetanilide

Triethylamine (0.65 ml, 4.65 mmol) was added to a solution of 200 mg (1.16 mmol) of 4-bromoaniline in tetrahydrofuran (2 ml), and the mixture was stirred at room temperature for 5 min. Acetyl chloride (0.165 ml, 2.33 mmol) was added thereto, and the mixture was stirred at room temperature for 17 hr. The reaction was stopped by adding a saturated aqueous sodium hydrogencarbonate solution, and the reaction solution Was extracted with ethyl acetate. The organic layer was washed with water and saturated brine in that order, was dried over anhydrous sodium sulfate and was filtered. The filtrate was concentrated under the reduced pressure, and the residue was purified by column chromatography on silica gel (chloroform:methanol=20:1) to give 249 mg (yield 99%) of the title compound.

1. stirringthe mixture was stirred at room temperature for 17 hr
2. extractionthe reaction solution Was extracted with ethyl acetate
3. washThe organic layer was washed with water and saturated brine in that order
4. dry with materialwas dried over anhydrous sodium sulfate
5. filtrationwas filtered
6. concentrationThe filtrate was concentrated under the reduced pressure
7. customthe residue was purified by column chromatography on silica gel (chloroform:methanol=20:1)

ORD-Eintrag

ord-085ac530f34a43b0b2bf97b536dc3451

Quelldatensatz

uspto-grants-2011_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07871982B2