Hydrazine hydrate (1:1) → 2-Hydrazinyl-4-methylpyridine

HRID 876463Notes

Reaction equation

HRID 876463 reaction equation
Cl[C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1.O.[NH2:10][NH2:11]>>[NH:10]([C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1)[NH2:11]

Participants

3

Conditions

Temperature
150 °C

Procedure

2-Chloro-4-methylpyridine (3.43 mL, 39.19 mmol) and hydrazine hydrate (19.07 mL, 391.9 mmol) were suspended together in a flask and heated to 150° C. for 72 hours. The mixture was concentrated in vacuo to an oil. The oil was taken up in EtOAc and the resulting solid was removed by vacuum filtration. The organic filtrate was washed with 40% aqueous NaOH (2×50 mL) and dried over Na2SO4, filtered and concentrated to provide the desired product (2.42 g, 54%) as a white solid.

Workup

  1. concentrationThe mixture was concentrated in vacuo to an oil
  2. customthe resulting solid was removed by vacuum filtration
  3. washThe organic filtrate was washed with 40% aqueous NaOH (2×50 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-782e67c865394de09e09d3ff2f101ad2
Source dataset
uspto-grants-2015_03
Patent number
US08987251B2

Reaction notes

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