反应详情

In a flask was added (R)-glycidol (0.994 g, 13.4 mmole) and triphenylphosphine (3.52 g, 13.4 mmole) and THF (20 ml, dried over molecular sieves), and 5-fluoro-2-nitrophenol (2.10 g, 13.4 mmole). The mixture was stirred until a homogeneous solution was obtained. The solution was cooled in an ice bath and diethylazodicarboxylate (DEAD, 2.11 ml, 13.4 mmole) was added dropwise over a few minutes. After completed addition, the flask was allowed to reach room temperature and stirred for an additional 2 hours. The solvent was removed in vaccuo and to the residue was added chloroform (5-10 ml). The precipitate (PPh3O) was removed by filtration and the solid was washed with an additional amount of chloroform (5-10 ml). The filtrate was added to a flash column (SiO2, Heptane:Ethyl acetate 4:1), and purified to give 2.02 g (71%) of the sub-title compound as a crystalline material after concentration of pure fractions.

1. customwas obtained
2. temperatureThe solution was cooled in an ice bath
3. additionaddition
4. customto reach room temperature
5. stirringstirred for an additional 2 hours
6. customThe solvent was removed in vaccuo and to the residue
7. additionwas added chloroform (5-10 ml)
8. customThe precipitate (PPh3O) was removed by filtration
9. washthe solid was washed with an additional amount of chloroform (5-10 ml)
10. additionThe filtrate was added to a flash column (SiO2, Heptane:Ethyl acetate 4:1)
11. custompurified