تفاعل #53261
ord-e1c90daa1155484ba6cc1f2c570561b8
معادلة التفاعل
الكواشف
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المعالجة
- 1درجة الحرارةthe mixture was heated
- 2درجة الحرارةunder reflux for one hour
- 3أخرىThe organic layer was separated
- 4استخلاصthe aqueous layer was extracted with isopropyl ether
- 5غسيلwashed with water
- 6تجفيفa saturated aqueous sodium hydrogencarbonate solution and a saturated aqueous solution of sodium chloride and then dried over anhydrous magnesium sulfate
- 7أخرىAfter the solvent was removed in vacuo under reduced pressure
- 8أخرىthe 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.