反应详情

To a solution of 2,2,2-trifluoro-ethanol (250 mg, 2.47 mmol) in DMF (15 mL) was added sodium hydride (71.25 mg, 2.97 mmol, 1.2 equiv.) at 0° C. and stirred for 15 min at this temperature. Then, a solution of butyl (4-chloroquinolin-6-ylmethylene)-amine (preparation was described in example 27b) (244.2 mg, 0.99 mmol) in DMF (1.79 mL) was added at 0° C. After addition, the reaction mixture was allowed to warm to room temperature and stirred for 4 h. Then, the mixture was diluted with saturated ammonium chloride solution and the organic compound was extracted into ethyl acetate (3×50 mL). The combined extracts were washed with brine solution and dried over anhydrous magnesium sulfate. After filtration of the drying agent, the solvent was removed under the vacuum and the brown residue was dissolved in THF (5 mL) and 3 mL of HCl solution (3.0N) was added. The resulting solution was stirred for 4 h at room temperature. Then, it was neutralized with sodium bicarbonate solution to from suspension. The solids were collected by filtration and washed with water. After drying in air, 190 mg (30% yield) of 4-(2,2,2-trifluoro-ethoxy)-quinoline-6-carbaldehyde was isolated as a white solid: EI-HRMS m/e calcd for C12H8F3N2O2 (M+) 255.0507, found 255.0505.

1. additionAfter addition
2. stirringstirred for 4 h
3. extractionthe organic compound was extracted into ethyl acetate (3×50 mL)
4. washThe combined extracts were washed with brine solution
5. dry with materialdried over anhydrous magnesium sulfate
6. filtrationAfter filtration of the drying agent
7. customthe solvent was removed under the vacuum
8. dissolutionthe brown residue was dissolved in THF (5 mL)
9. addition3 mL of HCl solution (3.0N) was added
10. stirringThe resulting solution was stirred for 4 h at room temperature
11. filtrationThe solids were collected by filtration
12. washwashed with water
13. customAfter drying in air