Triethylamine → 4-Bromo-N-(3-iodo-phenyl)-butyramide

To a solution of 3-iodoaniline (1.5 g, 6.85 mmol) and triethylamine (1.34 mL, 9.59 mmol) in dichloromethane (28 mL) at 0° C. was added dropwise 4-bromobutyryl chloride (0.99 mL, 8.56 mmol). The reaction mixture was then stirred at room temperature overnight. The organic extract was washed with an aqueous 1M HCl solution, aqueous 1M NaOH solution and brine, dried (Na2SO4), filtered, concentrated under vacuum. The crude residue was purified by silica gel column chromatography using a gradient of EtOAc (0-15%) in cyclohexane to yield a sticky solid. Trituration in a mixture of cyclohexane and ether and then filtration give the title compound as a solid (1.61 g, 64%).

1. extractionThe organic extract
2. washwas washed with an aqueous 1M HCl solution, aqueous 1M NaOH solution and brine
3. dry with materialdried (Na2SO4)
4. filtrationfiltered
5. concentrationconcentrated under vacuum
6. customThe crude residue was purified by silica gel column chromatography
7. customto yield a sticky solid
8. filtrationfiltration

ORD record

ord-f7871a57384f4a538967d51a3894c02f

Source dataset

uspto-grants-2014_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08846712B2