Hydrochloric Acid → 1-cyclohexyl-1-methylhydrazine

HRID 1856765Notes

Reaction equation

HRID 1856765 reaction equation
[CH3:1][NH:2][CH:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1.Cl.[N:10]([O-])=O.[Na+].[OH-].[Na+].C(S(O)=O)(N)=N>CO.O>[CH3:1][N:2]([CH:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)[NH2:10]

Participants

8

Procedure

To a solution of N-methylcyclohexylamine (17 g) in a 6N aqueous hydrochloric acid solution (90 ml) is added dropwise an aqueous solution (60 ml) of sodium nitrite (20.7 g) at 60° C. The mixture is stirred at the same temperature for 2 hours, and diluted with methanol (300 ml). To the mixture are added an aqueous solution (100 ml) of sodium hydroxide (45 g) and formamidine sulfinic acid (39 g). The mixture is refluxed for 2 hours, and diluted with water (400 ml). The mixture is extracted three times with methylene chloride, and the extract is washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to remove the solvent. The residue is distilled under reduced pressure to give 1-methyl-1-cyclohexylhydrazine (10 g) as a colorless oil.

Workup

  1. temperatureThe mixture is refluxed for 2 hours
  2. extractionThe mixture is extracted three times with methylene chloride
  3. washthe extract is washed with a saturated aqueous sodium chloride solution
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customto remove the solvent
  7. distillationThe residue is distilled under reduced pressure

Sources & evidence

ORD record
ord-ea737e6fbd4c4793b872aff3760ac853
Source dataset
uspto-grants-2000_11
Patent number
US06143763

Reaction notes

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