Hydrogen Peroxide → 5-Ethyl-2-fluorophenol

A solution of 15.5 g of 4-ethylfluorobenzene and 14.6 g of N,N,N′N′-tetramethylethylenediamine in 500 ml of THF was cooled to −75° C. under a nitrogen atmosphere, and then 126 ml of s-butyllithium (0.99M, cyclohexane solution) was added and the mixture was stirred for 2 hours. After then adding 28 ml of trimethyl borate, the reaction mixture was warmed to room temperature and 14.4 ml of acetic acid was added. After stirring for 30 minutes, the reaction mixture was cooled to 0° C., and then 28.4 ml of 30% aqueous hydrogen peroxide was added and the mixture was stirred at room temperature for 18 hours. Next, 500 ml of saturated aqueous sodium sulfite was added to the reaction mixture and extraction was performed with 1 liter of diethyl ether. The organic layer was washed with 500 ml of water and 500 ml of saturated aqueous sodium chloride in that order and dried over anhydrous magnesium sulfate, the desiccating agent was filtered, and the filtrate was concentrated under reduced pressure. The residue was subjected to distillation to give the title compound (16.35 g) as a colorless liquid (boiling point: 76-80° C., 17 mmHg).

1. stirringAfter stirring for 30 minutes
2. temperaturethe reaction mixture was cooled to 0° C.
3. stirringthe mixture was stirred at room temperature for 18 hours
4. washThe organic layer was washed with 500 ml of water and 500 ml of saturated aqueous sodium chloride in that order
5. dry with materialdried over anhydrous magnesium sulfate
6. filtrationthe desiccating agent was filtered
7. concentrationthe filtrate was concentrated under reduced pressure
8. distillationThe residue was subjected to distillation

ORD record

ord-0da6bcaec0414c3a9b69a90c6b97da9b

Source dataset

uspto-grants-2010_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07816522B2