反应详情

Sodium hydride (787 mg, 55%, 18.0 mmol) was suspended in DMF (10 mL) under a nitrogen atmosphere, and a solution of DMF (5 mL) containing 4-hydroxybenzaldehyde (2.00 g, 16.4 mmol) was dropwise added thereto over 5 minutes at room temperature. A light yellow insoluble substance was precipitated immediately after the addition. After 5 minutes, a solution of DMF (5 mL) containing 2,2,2-trifluoroethyl 4-methylbenzenesulfonate (4.00 g, 17.2 mmol) was added dropwise thereto to give a brown solution. This brown solution was stirred at room temperature for 1 hour, and then water (100 mL) and ethyl acetate (150 mL) were added thereto. The organic layer was separated, further washed with water (50 mL) five times, with a 10% sodium hydroxide aqueous solution (50 mL) three times, and with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated to give a crude product. This crude product was purified by silica gel column chromatography (hexane:ethyl acetate, 5:1, v/v) to give 1.40 g of the title compound (light yellow oil, yield: 42%).

1. additionwas dropwise added
2. customA light yellow insoluble substance was precipitated immediately
3. additionafter the addition
4. waitAfter 5 minutes
5. additionwas added dropwise
6. customto give a brown solution
7. customThe organic layer was separated
8. washfurther washed with water (50 mL) five times, with a 10% sodium hydroxide aqueous solution (50 mL) three times
9. dry with materialwith saturated brine, and dried over anhydrous magnesium sulfate
10. customThe solvent was evaporated
11. customto give a crude product
12. customThis crude product was purified by silica gel column chromatography (hexane