6-Ethoxycarbonyl-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-4-one → 6-Methyl-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-4-ol
反応式
C(O[C:4]([N:6]1[CH2:11][C:10](=[O:12])[C:9]2[CH:13]=[CH:14][O:15][C:8]=2[CH2:7]1)=O)C.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[CH3:4][N:6]1[CH2:11][CH:10]([OH:12])[C:9]2[CH:13]=[CH:14][O:15][C:8]=2[CH2:7]1参加物
4
実験手順
A solution of 1.76 g of 6-ethoxycarbonyl-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-4-one prepared in the step 4 in 20 mL of dry THF was slowly dropped into an ice-cooled solution of 0.45 g of lithium aluminum hydride in 20 mL of dry THF. The reaction solution was gradually heated followed by heating to reflux for 30 minutes. The reaction solution was cooled, an excess of lithium aluminum hydride was decomposed by a gradual addition of ice thereto and the mixture was subjected to extraction with ethyl acetate. The organic layer was washed with a saturated solution of sodium chloride and dried over anhydrous magnesium sulfate and the solvent was evaporated therefrom in vacuo. The residue was purified by silica gel column chromatography to give 1.03 g of the objective compound.