反应详情

To 7-bromo-2-trifluoroacetyl-1,2,3,4-tetrahydroisoquinoline (8.1 g), 4-methylphenylboric acid (3.9 g), a 2 M aqueous solution of potassium carbonate (40 ml) and ethanol (40 ml) was added toluene (100 ml), and the resulting mixture was stirred at room temperature under an argon atmosphere for 30 minutes. Thereto was added tetrakis(triphenylphosphine)palladium (1.26 g), and the resulting mixture was refluxed under an argon atmosphere for 4.5 hours. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with water and an aqueous saturated solution of sodium chloride, and was then dried with anhydrous magnesium sulfate. After evaporation of the solvent under reduced pressure, methanol (200 ml) and a 2 M aqueous solution of potassium carbonate (50 ml) were added to the residue, and the resulting mixture was stirred overnight at room temperature. After concentration, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water and was then back-extracted with 1 N hydrochloric acid. The aqueous layer was made alkaline with a 1 N aqueous solution of sodium hydroxide, was then saturated with sodium chloride and was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated solution of sodium chloride and was dried with anhydrous magnesium sulfate. The resulting organic layer was evaporated under reduced pressure to remove the solvent to obtain 7-(4-methylphenyl)-1,2,3,4-tetrahydroisoquinoline (4.2 g) as colorless crystals.

1. temperaturethe resulting mixture was refluxed under an argon atmosphere for 4.5 hours
2. extractionThe reaction mixture was extracted with ethyl acetate
3. washthe organic layer was washed with water
4. dry with materialan aqueous saturated solution of sodium chloride, and was then dried with anhydrous magnesium sulfate
5. customAfter evaporation of the solvent under reduced pressure, methanol (200 ml)
6. additiona 2 M aqueous solution of potassium carbonate (50 ml) were added to the residue
7. stirringthe resulting mixture was stirred overnight at room temperature
8. concentrationAfter concentration
9. extractionthe reaction mixture was extracted with ethyl acetate
10. washThe organic layer was washed with water
11. extractionwas then back-extracted with 1 N hydrochloric acid
12. extractionsaturated with sodium chloride and was extracted with ethyl acetate
13. washThe organic layer was washed with an aqueous saturated solution of sodium chloride
14. dry with materialwas dried with anhydrous magnesium sulfate
15. customThe resulting organic layer was evaporated under reduced pressure
16. customto remove the solvent