1,3-Dibromo-5,5-dimethylhydantoin → 5-Bromo-2-ethoxy-3-(trifluoromethyl)pyridine

2-Ethoxy-3-trifluoromethyl-pyridine (900 mg, 4.71 mmol) and 1,3-dibromo-5,5-dimethylhydantoin (1.35 g, 4.71 mmol) were placed in a round-bottom flask. To this mixture was slowly added 10 mL trifluoroacetic acid. The mixture was stirred at ambient temperature for overnight. More 1,3-dibromo-5,5-dimethylhydantoin (540 mg, 1.9 mmol) was added and the reaction mixture was stirred at ambient temperature for another day. After the completion of the reaction, TFA solvent was evaporated in vacuo and the resulting residue was neutralized to pH 7 by the addition of saturated NaHCO3. The aqueous layer was extracted with dichloromethane three times and the combined extract was washed with brine, dried over sodium sulfate, and concentrated in vacuo to give a mixture of oil and white solid. The residue was redissolved into 20% EtOAc/Hexane, and the unsoluable white solid was filtered out. The filtrate was concentrated and then purified by column chromatography on silica gel (10% EtOAC/Hexane) to give 5-bromo-2-ethoxy-3-trifluoromethyl-pyridine as a colorless liquid (1.0 g, 79% yield). 1H-NMR (400 MHz, CDCl3): δ 1.41 (t, 3H, J=7.07), 4.46 (q, 2H, J=7.07), 7.94 (dd, 1H, J=0.51, J=2.53), 8.34 (dd, 1H, J=0.51, J=2.53).

1. stirringthe reaction mixture was stirred at ambient temperature for another day
2. customwas evaporated in vacuo
3. additionthe resulting residue was neutralized to pH 7 by the addition of saturated NaHCO3
4. extractionThe aqueous layer was extracted with dichloromethane three times
5. extractionthe combined extract
6. washwas washed with brine
7. dry with materialdried over sodium sulfate
8. concentrationconcentrated in vacuo
9. customto give
10. additiona mixture of oil and white solid
11. filtrationthe unsoluable white solid was filtered out
12. concentrationThe filtrate was concentrated
13. custompurified by column chromatography on silica gel (10% EtOAC/Hexane)

ORD record

ord-06cd8a8043644830bda434aefcf682c8

Source dataset

uspto-grants-2011_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08013001B2