Ethyl Acetate → HCID 58820194, compound

To 2,4 difluorophenol (Aldrich Chemical Co.) (2.68 mL, 1.1 eq) in THF (60 mL) at 0° C. was added sodium hydride (60% in oil) (1.123 g, 1.1 eq), and the resulting mixture was stirred from 0° C. to room temperature over 1 hour. This solution was then added to compound (1A) (5.79 g, 26.7 mmol), and the resulting mixture was heated at reflux for 2 hours. TLC analysis confirmed that the reaction was complete, and the mixture was cooled to room temperature. EtOAc (300 mL) and water (100 mL) were added, the resulting mixture was partitioned, and the layers were separated. The organic layer was washed with water (3×100 mL) and brine (1×100 mL). Then the EtOAc layer was dried over magnesium sulfate, filtered, concentrated, and pumped to give the titled compound (1B) as an off-white powder (7.99 g, M+=310, Mp=90.2–91.4° C.)

1. temperaturethe resulting mixture was heated
2. temperatureat reflux for 2 hours
3. customthe resulting mixture was partitioned
4. customthe layers were separated
5. washThe organic layer was washed with water (3×100 mL) and brine (1×100 mL)
6. dry with materialThen the EtOAc layer was dried over magnesium sulfate
7. filtrationfiltered
8. concentrationconcentrated

ORD record

ord-3fddf5fc3147439e9e59f4b03d968e9c

Source dataset

uspto-grants-2007_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07189731B2