Reacción #366343

Ecuación de reacción

diisopropyl ether

(1R)-1-[2-(2-fluorophenyl)-2-oxiranyl]ethanol

triphenylphosphine

3,5-dinitrobenzoic acid

diethyl azodicarboxylate

→

[(1S)-1-[(2R)-2-(2-fluorophenyl)-2-oxiranyl]ethyl] 3,5-dinitrobenzoate

Disolventes

tetrahydrofuran

water

ethyl acetate

Condiciones de reacción

Tratamiento posterior

1. 1
   ExtracciónThe separated aqueous layer was extracted with ethyl acetate (600 ml, 400 ml)
2. 2
   Lavadowashed with water
3. 3
   Secadoa saturated aqueous solution of sodium chloride successively, dried over anhydrous magnesium sulfate
4. 4
   Concentraciónconcentrated
5. 5
   OtroThe residue was purified by silica gel chromatography (eluent: hexane/ethyl acetate=5/1)
6. 6
   Otrorecrystallized from ethyl acetate

Procedimiento

2-(2-Fluorophenyl)-2-[(l1R)-1-(3,4,5,6-tetrahydro-2H-pyran-2-yl)oxyethyl] oxirane (synthesized by the method described in EP0548553A) was converted into (1R)-1-[2-(2-fluorophenyl)-2-oxiranyl]ethanol by the method described in Reference Example 1. To an ice-cooled solution of this compound (34.77 g) in tetrahydrofuran (600 ml) were added triphenylphosphine (127.21 g), 3,5-dinitrobenzoic acid (102.88 g) and diethyl azodicarboxylate (84.47 g). The mixture was stirred at room temperature for 7 hours under an argon atmosphere, and then ethyl acetate (600 ml), diisopropyl ether (100 ml) and water (800 ml) were added. The separated aqueous layer was extracted with ethyl acetate (600 ml, 400 ml). The organic layers were combined, washed with water and a saturated aqueous solution of sodium chloride successively, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel chromatography (eluent: hexane/ethyl acetate=5/1) and recrystallized from ethyl acetate to give [(1S)-1-[(2R)-2-(2-fluorophenyl)-2-oxiranyl]ethyl] 3,5-dinitrobenzoate (23.15 g) as colorless needles.

Fuente