反应详情

4-[2-(Methyloxy)-2-oxoethyl]benzoic acid (150) (1.0 g, 5.15 mmol) was dissolved in CH2Cl2 (25 mL). Oxalyl chloride (0.92 mL, 10.3 mmol) was added dropwise, followed by addition of two drops of DMF. The reaction mixture was stirred at room temperature for 2 h. CH2Cl2 and the excess of oxalyl chloride were removed under vacuum. The residue was dissolved in CH2Cl2 (15 mL) with anisole (0.74 mL, 6.70 mmol). Cooled in an ice bath, AlCl3 (1.04 g, 7.73 mmol) was added in portions. The mixture was stirred at 0° C. for 4 h, then stirred at room temperature for 20 minutes. Poured into 1 N HCl (25 mL) with ice, the mixture was extracted with CH2Cl2 (2×60 mL). The combined CH2Cl2 extract was washed with saturated aqueous NaHCO3, brine, dried over Na2SO4, filtered, and the filtrate was concentrated to give yellow oil. The crude product was purified by chromatography on a silica gel column eluted with hexanes:EtOAc (5:1) to give 1.00 g (68%) of compound 151 as colorless oil. 1H NMR (400 MHz, CDCl3): δ 3.71 (s, 2H), 3.72 (s, 3H), 3.88 (s, 3H), 6.96 (d, J=8.8 Hz, 2H), 7.38 (d, J=8.0 Hz, 2H), 7.72 (d, J=8.1 Hz, 2H), 7.82 (d, J=8.8 Hz, 2H). LCMS (ESI): m/z, 285 (M+H)+, 283 (M−H)−.

1. customCH2Cl2 and the excess of oxalyl chloride were removed under vacuum
2. temperatureCooled in an ice bath
3. stirringThe mixture was stirred at 0° C. for 4 h
4. stirringstirred at room temperature for 20 minutes
5. extractionthe mixture was extracted with CH2Cl2 (2×60 mL)
6. extractionThe combined CH2Cl2 extract
7. washwas washed with saturated aqueous NaHCO3, brine
8. dry with materialdried over Na2SO4
9. filtrationfiltered
10. concentrationthe filtrate was concentrated
11. customto give yellow oil
12. customThe crude product was purified by chromatography on a silica gel column
13. washeluted with hexanes:EtOAc (5:1)