Ethyl 2-(3-nitropyridin-2-yl)acetate → Ethyl 2-(3-aminopyridin-2-yl)acetate
Reaction equation
[N+:1]([C:4]1[C:5]([CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])=[N:6][CH:7]=[CH:8][CH:9]=1)([O-])=O>C(O)C.[Pd]>[NH2:1][C:4]1[C:5]([CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])=[N:6][CH:7]=[CH:8][CH:9]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Under an atmosphere of nitrogen, Pd/C (10%, 1.36 g) was added to a round bottom flask. Ethyl 2-(3-nitro-pyridin-2-yl)-acetate (8.6 g, 0.41 mol) was dissolved in ethanol (200 mL) and added to the reaction vessel. The reaction was placed under an atmosphere of hydrogen and stirred at room temperature for 30 min. The reaction was filtered through celite, and the filtrate was concentrated in vacuo to afford the title compound as a tan solid (6.94 g, 94% yield).
Workup
- additionadded to the reaction vessel
- filtrationThe reaction was filtered through celite
- concentrationthe filtrate was concentrated in vacuo
Sources & evidence
- ORD record
- ord-2b7e17419dac41e19437abef043cb72c
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06369086B1
Reaction notes
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