反应详情

Add butylzinc bromide (49.3 mL, 24.6 mmol, 0.5 M in THF) followed by Pd(dppf)2Cl2 dichloromethane complex (1.01 g, 1.23 mmol) to a solution of 3-bromo-5-fluorobenzaldehyde (5.00 g, 24.6 mmol) in tetrahydrofuran (123.1 mL). Stir at room temperature in a sealed vessel flushed with nitrogen for 18 hours. Add saturated aqueous ammonium chloride (125 mL). Separate the layers and extract the aqueous layer with ethyl acetate (1×300 mL). Wash combined organic layers with saturated aqueous sodium chloride, dry over magnesium sulfate and concentrate under reduced pressure. Subject residue to silica gel chromatography, eluting with 0-10% ethyl acetate in hexanes to provide the title compound (3.43 g, 77.3%).

1. customflushed with nitrogen for 18 hours
2. customSeparate the layers
3. extractionextract the aqueous layer with ethyl acetate (1×300 mL)
4. washWash
5. dry with materialdry over magnesium sulfate
6. concentrationconcentrate under reduced pressure
7. washSubject residue to silica gel chromatography, eluting with 0-10% ethyl acetate in hexanes