تفاعل #53261

ord-e1c90daa1155484ba6cc1f2c570561b8

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was heated
  2. 2
    درجة الحرارةunder reflux for one hour
  3. 3
    أخرىThe organic layer was separated
  4. 4
    استخلاصthe aqueous layer was extracted with isopropyl ether
  5. 5
    غسيلwashed with water
  6. 6
    تجفيفa saturated aqueous sodium hydrogencarbonate solution and a saturated aqueous solution of sodium chloride and then dried over anhydrous magnesium sulfate
  7. 7
    أخرىAfter the solvent was removed in vacuo under reduced pressure
  8. 8
    أخرىthe residue was purified by a silica gel column chromatography (silica gel 70 g, hexane: ethyl acetate=100:15)

الإجراء التجريبي

To a solution of the benzyl ester (3.11 g) obtained in Synthesis Example 80 in methanol (70 ml) was added p-toluenesulfonic acid (0.35 g) and the mixture was heated under reflux for one hour. After cooling to room temperature, isopropyl ether and water were added thereto. The organic layer was separated and the aqueous layer was extracted with isopropyl ether. The extract was combined with the organic layer and washed with water, a saturated aqueous sodium hydrogencarbonate solution and a saturated aqueous solution of sodium chloride and then dried over anhydrous magnesium sulfate. After the solvent was removed in vacuo under reduced pressure, the residue was purified by a silica gel column chromatography (silica gel 70 g, hexane: ethyl acetate=100:15) to afford 1.38 g of benzyl 6-methyl-3-hydroxyheptanoate.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06858585B1uspto-grants-2005_02