反应详情

232 g (1 mol) of 2-(hydroxymethyl)-5-(phenylmethoxy)-4H-pyran-4-one was put into a 10 l stirring flask containing 6.6 l of acetone and 400 ml of water. The clear solution was cooled to +5° C. by means of an ice bath. While maintaining the temperature at +5° C. to 10° C., 640 ml of Jones reagent (202 g CrO3, 600 ml water, 174 ml H2SO4) was added dropwise over a period of 1 hour. Stirring was continued for 2 hours without cooling. The reaction mixture was filtered through a glass frit and the dark green residue washed with 500 ml of acetone. The filtrate was then evaporated until all of the acetone was removed. To the aqueous, partly crystalline product was added 1.2 l of methanol, and this mixture was then heated to its boiling point. The resulting clear dark green solution was placed in an ice bath and the product allowed to crystallize. The crystalline product was filtered and washed with 500 ml of a cold solvent mixture consisting of 250 ml of methanol +250 ml of water and finally dried. Yield: 195 g. From the mother liquor, a further 5% of the product could be isolated.

1. temperatureThe clear solution was cooled to +5° C. by means of an ice bath
2. temperatureWhile maintaining the temperature at +5° C. to 10° C.
3. stirringStirring
4. temperaturewithout cooling
5. filtrationThe reaction mixture was filtered through a glass frit
6. washthe dark green residue washed with 500 ml of acetone
7. customThe filtrate was then evaporated until all of the acetone
8. customwas removed
9. additionTo the aqueous, partly crystalline product was added 1.2 l of methanol
10. temperaturethis mixture was then heated to its boiling point
11. customThe resulting clear dark green solution was placed in an ice bath
12. customto crystallize
13. filtrationThe crystalline product was filtered
14. washwashed with 500 ml of a cold solvent mixture
15. customfinally dried