Ammonium Hydroxide → 1-(2-Amino-3-methylphenyl)ethan-1-one

HRID 1702512Notes

Reaction equation

HRID 1702512 reaction equation
C([NH:4][C:5]1[C:10]([C:11](=[O:13])[CH3:12])=[CH:9][CH:8]=[CH:7][C:6]=1[CH3:14])(=O)C.[OH-].[NH4+]>O.C(O)C.Cl.S(=O)(=O)(O)O>[CH3:14][C:6]1[CH:7]=[CH:8][CH:9]=[C:10]([C:11](=[O:13])[CH3:12])[C:5]=1[NH2:4]

Participants

7

Reactant 2

HCID 14923Ammonium HydroxideHCID 15581073HCID 15581073, compound

Product 1

HCID 1796281-(2-Amino-3-methylphenyl)ethan-1-oneYield 83%

Reagents, catalysts & solvents 4

HCID 313Hydrochloric AcidSolventHCID 702EthanolSolventHCID 962WaterSolventHCID 1118Sulfuric AcidSolvent

Procedure

N-Acetyl-2-methyl-6-acetylaniline (76.1 g) in water (300 ml), ethanol (300 ml), concentrated hydrochloric acid (300 ml) and concentrated sulfuric acid (15 ml) were refluxed for 24 hours. The solution was cooled and concentrated ammonium hydroxide was added to pH 10. The solution was extracted with dichloromethane. The extracts were dried (MgSO4) and stripped. 2-methyl-6-acetylaniline (49.3 g) was obtained as a tan solid.

Workup

  1. temperatureThe solution was cooled
  2. extractionThe solution was extracted with dichloromethane
  3. dry with materialThe extracts were dried (MgSO4)

Sources & evidence

ORD record
ord-6890fd73bb97432fa76e8d9a94a087e4
Source dataset
uspto-grants-1982_09
Patent number
US04348222

Reaction notes

Loading…