Sodium Bicarbonate → 2,4-Dichloropyridin-3-amine

HRID 1401120Notes

Reaction equation

HRID 1401120 reaction equation
[Cl:1][C:2]1[C:7]([N+:8]([O-])=O)=[C:6]([Cl:11])[CH:5]=[CH:4][N:3]=1.C([O-])(O)=O.[Na+]>CC(O)=O.[Fe]>[CH:5]1[C:6]([Cl:11])=[C:7]([NH2:8])[C:2]([Cl:1])=[N:3][CH:4]=1

Participants

5

Conditions

Temperature
40 °C

Procedure

2.4-Dichloro-3-nitropyridine c (2.058 g, 10.7 mmol) was dissolved in HOAc (10 mL) under nitrogen. Iron powder (1.9191 g, 34.4 mmol) was added. The sample was heated at 40° C. for two hours. The reaction mixture was poured onto ice and then NaHCO3 was added to give a neutral solution. The sample was extracted with EtOAc (3×100 mL). The EtOAc extracts were washed with saturated NaHCO3 (1×100 mL). The combined aqueous layers were back extracted once with 100 mL EtOAc. The combined EtOAc extracts were dried over MgSO4, filtered, and concentrated to give 3-amino-2-4-dichloropyridine d (1.510 g, 9.26 mmol, 87%).

Workup

  1. additionThe reaction mixture was poured onto ice
  2. customto give a neutral solution
  3. extractionThe sample was extracted with EtOAc (3×100 mL)
  4. washThe EtOAc extracts were washed with saturated NaHCO3 (1×100 mL)
  5. extractionThe combined aqueous layers were back extracted once with 100 mL EtOAc
  6. dry with materialThe combined EtOAc extracts were dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-80fa24f15f994e60a3576afafb9c5e3a
Source dataset
uspto-grants-2014_12
Patent number
US08907092B2

Reaction notes

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