反应详情

α-[[(4-methoxybenzyl)amino]methyl]-3,4-dimethoxybenzyl alcohol (950 mg) was dissolved in 7.2 ml of trifluoroacetic acid, and after adding thereto 0.22 ml of conc. sulfuric acid under cie dooling, the reaction was allowed to react for 45 minutes. The reaction solution was concentrated, and subjected to azeotropic distillation with toluene 2 times. After adding chloroform, the mixture was basified by addition of 28% aqueous ammonia under ice cooling. By a separating procedure, the chloroform layer was collected, washed with water, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue obtained was subjected to silica gel column chromatography (chlroform-methanol-28% aqueous ammonia=15:1:0.1), giving 790 mg of 6-methoxy-4-(3,4-dimethoxyphenyl)-1,2,3,4-tetrahydroisoquinoline as oily matter.

1. additionafter adding
2. customto react for 45 minutes
3. concentrationThe reaction solution was concentrated
4. distillationsubjected to azeotropic distillation with toluene 2 times
5. additionAfter adding chloroform
6. additionthe mixture was basified by addition of 28% aqueous ammonia under ice cooling
7. customBy a separating procedure, the chloroform layer was collected
8. washwashed with water
9. dry with materialdried over anhydrous sodium sulfate
10. distillationThe solvent was distilled off
11. customthe residue obtained