2-(3-Nitrophenyl)pyridine → 3-(2-Pyridyl)aniline

HRID 1075452Notes

Reaction equation

HRID 1075452 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=2)[CH:7]=[CH:8][CH:9]=1)([O-])=O.[H][H]>[Pd].C(O)C>[N:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[C:6]1[CH:5]=[C:4]([CH:9]=[CH:8][CH:7]=1)[NH2:1]

Participants

5

Procedure

To a solution of 2-(3-nitrophenyl)pyridine (prepared as described in J. Chem. Soc. 1958 p. 1759) (12.7g, 63.5mmol) in abs. ethanol is added palladium catalyst (1.3g 5% Pd on activated carbon) and the mixture is hydrogenated at ambient pressure until the hydrogen uptake has ceased. The mixture is filtered through celite and the filtrate is concentrated under reduced pressure. The residue is purified by column-chromatography on silica gel using a mixture of ethyl acetate and petroleum ether (9:1)as the eluent to afford 2f (9.5g, 88%) as a light brown oil.

Workup

  1. filtrationThe mixture is filtered through celite
  2. concentrationthe filtrate is concentrated under reduced pressure
  3. customThe residue is purified by column-chromatography on silica gel using
  4. additiona mixture of ethyl acetate and petroleum ether (9

Sources & evidence

ORD record
ord-daaf52169366414483f2601633266ee4
Source dataset
uspto-grants-1999_05
Patent number
US05902813

Reaction notes

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