Реакция #2439948

Уравнение реакции

5-(4-Nitro-benzoyl)-1,3-dihydro-indol-2-one

keto-aniline

→

5-(3-Amino-benzoyl)-1,3-dihydro-indol-2-one

Растворители

MeOH

Условия реакции

Обработка

1. 1
   Другоеto remove any O2(g)
2. 2
   workup.ADDITIONwas then charged with H2(g)
3. 3
   Другоеconsumption of the starting material
4. 4
   Другоеthe reaction
5. 5
   Другоеimmediately upon complete consumption of the starting material
6. 6
   workup.WAITto run for 0.75-1.0 hours
7. 7
   Фильтрацияafter which, the reaction mixture was filtered over celite and
8. 8
   Концентрированиеconcentrated in vacuo
9. 9
   Другоеresulting in a yellowish solid
10. 10
    ДругоеThe crude solid was purified
11. 11
    Другоеby triturating with MeOH
12. 12
    Фильтрацияwas filtered away from the insoluble over reduced alcohol by-product

Методика

5-(4-Nitro-benzoyl)-1,3-dihydro-indol-2-one (1.51 g, 5.28 mmol) was dissolved in MeOH (600 mL). 10% Pd/C (0.150 g) was added to the flask and then placed under vacuum to remove any O2(g). The reaction mixture was kept under reduced pressure for ˜5 min and was then charged with H2(g). This evacuation/H2(g) fill procedure was repeated twice. The reaction mixture changed from a cloudy grayish/black color to a translucent dark green/black color, signifying complete consumption of the starting material. As the desired ketone product was prone to over-reduction to the alcohol, stopping the reaction immediately upon complete consumption of the starting material limited the amount over-reduction that occurred. The reaction was allowed to run for 0.75-1.0 hours after which, the reaction mixture was filtered over celite and concentrated in vacuo resulting in a yellowish solid that contained the desired keto-aniline product plus ˜5% of the overreduced alcohol-aniline. The crude solid was purified by triturating with MeOH. The desired keto-aniline product, 5-(3-Amino-benzoyl)-1,3-dihydro-indol-2-one was soluble in MeOH and was filtered away from the insoluble over reduced alcohol by-product. In vacuo concentration of the methanolic filtrate provided pure 5-(3-Amino-benzoyl)-1,3-dihydro-indol-2-one in 72% (0.957 g, 3.80 mmol) yield.

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