反应详情

To a solution of (8-bromo-6-fluoro-3,4-dihydro-2H-chromen-2-yl)methyl 4-methylbenzenesulfonate (0.33 g, 0.795 mmol) and 2-chlorophenylboronic acid (249 mg, 1.589 mmol) in dioxane (9 mL) was added a solution of potassium carbonate (329 mg, 2.38 mmol) in water (3 mL) and the mixture purged with nitrogen for 20 minutes. Trans-dichlorobis(tri-o-tolylphosphine)palladium (II) (31.2 mg, 0.0397 mmol) was added and the reaction mixture heated to reflux for 18 hours. The cooled reaction mixture was then partitioned between ethyl acetate (100 mL) and 2.0 M aqueous sodium hydroxide (100 mL). The organic layer was separated, washed with water (100 mL) and saturated brine (100 mL), dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford a yellow syrup. Purification by flash chromatography using a solvent gradient of 5 to 20% ethyl acetate in hexane gave 253 mg (71%) of toluene-4-sulfonic acid 8-(2-chloro-phenyl)-6-fluoro-chroman-2-ylmethyl ester as a colorless syrup. MS (ESI) m/z 464 ([M+NH4]+).

1. customthe mixture purged with nitrogen for 20 minutes
2. temperaturethe reaction mixture heated
3. temperatureto reflux for 18 hours
4. customThe cooled reaction mixture
5. customwas then partitioned between ethyl acetate (100 mL) and 2.0 M aqueous sodium hydroxide (100 mL)
6. customThe organic layer was separated
7. washwashed with water (100 mL) and saturated brine (100 mL)
8. dry with materialdried over magnesium sulfate
9. filtrationfiltered
10. concentrationconcentrated under reduced pressure
11. customto afford a yellow syrup
12. customPurification by flash chromatography