تفاعل #1093486
ord-810915b0e2bf4c31a80cb453c83aebd4
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.STIRRINGThe reaction was stirred at room temperature for 3 hours or until the solution
- 2أخرىthe completion of the reaction which
- 3workup.STIRRINGstirred for an additional hour or until solution
- 4استخلاصto extract the products and 1N HCl
- 5workup.DISSOLUTIONto dissolve the salts
- 6استخلاصThe organic extract
- 7غسيلwas washed with 1N HCl (50 mL×3) and brine (50 mL)
- 8تجفيفdried over Na2SO4
- 9أخرىthe solvent was removed under reduced pressure
- 10أخرىto obtain the crude product
الإجراء التجريبي
(−)-Isopulegol (60 mg) was dissolved in DMF (4 mL), and OsO4 (0.05 mL, 2.5% in tBuOH) was added and stirred for 5 min. OXONE (0.235 g) was added in one portion and the reaction had a final volume (6 mL). The reaction was stirred at room temperature for 3 hours or until the solution becomes colorless. This usually marks the completion of the reaction which was verified by TLC or GC. Na2SO3 (360 mg) was added, to reduce the remaining Os(VIII), and stirred for an additional hour or until solution became dark brown/black. EtOAc was added to extract the products and 1N HCl was used to dissolve the salts. The organic extract was washed with 1N HCl (50 mL×3) and brine (50 mL), dried over Na2SO4, and the solvent was removed under reduced pressure to obtain the crude product. (1R, 2R, 5R)-2-Acetyl-5-methyl cyclohexanol and (1R, 2R, 5R)-2-Acetyl-5-methyl cyclohexanyl formate were obtained in 44% and 34% yield respectively after purification by silica gel column chromatography.