Dimethylformamide → 2,4-Difluoro-3-(hydroxymethyl)phenol

Temperature

-78 °C

To a stirred solution of tert-butyl(2,4-difluorophenoxy)dimethylsilane (J. Med. Chem. 1993, 36, 3947, 1.50 g, 6.14 mmol) in tetrahydrofuran (30 mL) was added a 1.57 M solution of n-butyllithium in hexane (4.69 mL, 7.37 mmol) at −78° C. over 10 minutes, and the mixture was stirred at −78° C. for 2 h. To the mixture, N,N-dimethylformamide (0.950 mL, 2.28 mmol) was added at −78° C. The mixture was stirred at −78° C. for 1 h, allowed to warm to room temperature and stand at room temperature for 16 h. The mixture was diluted with methanol (20 mL), and to the mixture was added sodium borohydride (696 mg, 18.4 mmol) at 0° C. The mixture was stirred at room temperature for 1.5 h. The reaction was quenched by addition of aqueous ammonium chloride at 0° C. to be pH=7. The mixture was extracted with diethyl ether (200 mL) and the organic layer washed with brine, dried over magnesium sulfate and evaporated. The residue was purified by column chromatography on silica gel (100 g) eluting with hexane/ethyl acetate (2/1) to afford 410 mg (42%) of the title as a colorless oil:

1. stirringThe mixture was stirred at −78° C. for 1 h
2. temperatureto warm to room temperature
3. waitstand at room temperature for 16 h
4. stirringThe mixture was stirred at room temperature for 1.5 h
5. customThe reaction was quenched by addition of aqueous ammonium chloride at 0° C.
6. extractionThe mixture was extracted with diethyl ether (200 mL)
7. washthe organic layer washed with brine
8. dry with materialdried over magnesium sulfate
9. customevaporated
10. customThe residue was purified by column chromatography on silica gel (100 g)
11. washeluting with hexane/ethyl acetate (2/1)
12. customto afford 410 mg (42%) of the title as a colorless oil

ORD record

ord-2be136926b9540868074aff0d572f222

Source dataset

uspto-grants-2008_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07354925B2