反应详情

5-Methoxy-2-naphthoic acid (49 7 g; 0 246 mol, J Med Chem 1993, 36, 2485) in glacial acetic acid (450 ml) and in 48% strength aqueous hydrobromic acid solution (450 ml) is heated to reflux for 15 h After cooling, the reaction mixture is concentrated in vacuo and is extracted with dichloromethane after addition to water The organic phase is washed with water, dried over MgSO4 and concentrated in vacuo. The residue is dissolved in MeOH (1.6 l) The solution is saturated with hydrogen chloride (about 1 h), the reaction mixture heating to reflux temperature. The solvent is then stripped off in vacuo, the residue is taken up in ethyl acetate, and the mixture is washed with satd NaCl solution, dried (MgSO4) and concentrated in vacuo. The residue is chromatographed on silica gel using dichloromethane:ethyl acetate (20:1). The product thus obtained is stirred with dichloromethane/petroleum ether, filtered off with suction and dried in vacuo.

1. temperatureto reflux for 15 h
2. temperatureAfter cooling
3. concentrationthe reaction mixture is concentrated in vacuo
4. extractionis extracted with dichloromethane
5. additionafter addition to water The organic phase
6. washis washed with water
7. dry with materialdried over MgSO4
8. concentrationconcentrated in vacuo
9. dissolutionThe residue is dissolved in MeOH (1.6 l) The solution
10. customis saturated with hydrogen chloride (about 1 h)
11. temperaturethe reaction mixture heating
12. temperatureto reflux temperature
13. washthe mixture is washed with satd NaCl solution
14. dry with materialdried (MgSO4)
15. concentrationconcentrated in vacuo
16. customThe residue is chromatographed on silica gel
17. customThe product thus obtained
18. filtrationfiltered off with suction
19. customdried in vacuo