Reaktion #729107

Reaktionsgleichung

5-bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinoline

→

2-methyl-1,2,3,4-tetrahydroisoquinolin-8-amine

Lösungsmittel

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeHydrogen gas was bubbled into the mixture The resulting solution
2. 2
   Sonstigeto react
3. 3
   FiltrationA filtration
4. 4
   EinengenThe filtrate was concentrated by evaporation under vacuum
5. 5
   Sonstigea rotary evaporator
6. 6
   workup.ADDITIONThe resulting solution was diluted with 50 mL of Na2CO3 (10%)
7. 7
   ExtraktionThe resulting solution was extracted four times with 50 mL of ethyl acetate
8. 8
   Trocknendried over Na2SO4
9. 9
   SonstigeThe residue was purified
10. 10
    Waschenby eluting through a column with a 50:1 CH2Cl2/MeOH solvent system
11. 11
    SonstigeThis resulted in 2.57 g (89%) of 2-methyl-1,2,3,4-tetrahydroisoquinolin-8-amine as a light yellow oil

Vorschrift

Into a 250 mL 3-necked round bottom flask was added a solution of 5-bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinoline (4.85 g, 17.89 mmol) in CH3OH/Et3N(anhydrous) (150/15 mL). To the mixture was added Pd/C (4.5 g). Hydrogen gas was bubbled into the mixture The resulting solution was allowed to react, with stirring, for 3 hours while the temperature was maintained at room temperature. The reaction progress was monitored by TLC (ethyl acetate/petroleum ether=1:1). A filtration was performed. The filtrate was concentrated by evaporation under vacuum using a rotary evaporator. The resulting solution was diluted with 50 mL of Na2CO3 (10%). The resulting solution was extracted four times with 50 mL of ethyl acetate and the organic layers combined and dried over Na2SO4. The residue was purified by eluting through a column with a 50:1 CH2Cl2/MeOH solvent system. This resulted in 2.57 g (89%) of 2-methyl-1,2,3,4-tetrahydroisoquinolin-8-amine as a light yellow oil.

Quelle