4-Bromo-2-methylaniline → (4-bromo-2-methylphenyl)hydrazine

HRID 1880397Notes

Reaction equation

HRID 1880397 reaction equation
[Br:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([CH3:9])[CH:3]=1.[N:10]([O-])=O.[Na+].Cl[Sn]Cl.[OH-].[Na+]>Cl.O>[Br:1][C:2]1[CH:8]=[CH:7][C:5]([NH:6][NH2:10])=[C:4]([CH3:9])[CH:3]=1

Participants

7

Conditions

Temperature
80 °C

Procedure

4-Bromo-2-methylaniline (2.00 g, 10.8 mmol) was dissolved in conc. HCl (10 mL) and heated to 80° C. for 30 minutes. The reaction was then cooled to 5° C. and a solution of NaNO2 (781 mg, 10.8 mmol) in water (4 mL) was added over 10 minutes. The resulting mixture was stirred at 5° C. for 30 minutes before addition of SnCl2 (15.3 g, 80.6 mmol) in conc. HCl (8 mL) over 10 minutes. The mixture was stirred at room temperature for 45 minutes before addition of 50% aqueous NaOH. The resulting precipitate was isolated by filtration and the filtrate was extracted with CH2Cl2. The combined organic phases were dried over MgSO4, filtered and concentrated to provide (4-bromo-2-methylphenyl)hydrazine (1.08 g, 50%).

Workup

  1. temperatureThe reaction was then cooled to 5° C.
  2. customThe resulting precipitate was isolated by filtration
  3. extractionthe filtrate was extracted with CH2Cl2
  4. dry with materialThe combined organic phases were dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-cc7efe8ccc1549e78b4de6e425f44668
Source dataset
uspto-grants-2012_11
Patent number
US08318762B2

Reaction notes

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