Sodium Acetate → 2,3-Dichloro-6-methylaniline

HRID 1031386Notes

Reaction equation

HRID 1031386 reaction equation
[Cl:1][C:2]1[C:8]([Cl:9])=[C:7](Br)[CH:6]=[C:5]([CH3:11])[C:3]=1[NH2:4].C([O-])(=O)C.[Na+]>C(O)(=O)C.C(O)C.[Pd]>[Cl:1][C:2]1[C:8]([Cl:9])=[CH:7][CH:6]=[C:5]([CH3:11])[C:3]=1[NH2:4]

Participants

5

Procedure

A slurry of 6.50 g (25.5 mmol) of 2,3-dichloro-4-bromo-6-methylaniline and 8.37 g (102 mmol) of sodium acetate in 120 ml of acetic acid-ethanol (1:1, v/v) was treated with 0.55 g of 5% palladium on carbon. The mixture was hydrogenated in a Parr hydrogenation apparatus at an initial pressure of 50 psi for 10 minutes. The reaction mixture was filtered, and the filtrate was concentrated by evaporation at reduced pressure. The residue was partitioned between ether and water, and the organic layer was washed with 5% aqueous sodium hydroxide, dried and evaporated at reduced pressure. The residue was purified by Kugelrohr distillation to afford 4.00 g (89%) of the desired product as a colorless oil, b.p. 60°-70° C. (0.15 mm). IR and 1H NMR spectra were in agreement with the assigned structure.

Workup

  1. customfor 10 minutes
  2. filtrationThe reaction mixture was filtered
  3. concentrationthe filtrate was concentrated by evaporation at reduced pressure
  4. customThe residue was partitioned between ether and water
  5. washthe organic layer was washed with 5% aqueous sodium hydroxide
  6. customdried
  7. customevaporated at reduced pressure
  8. distillationThe residue was purified by Kugelrohr distillation

Sources & evidence

ORD record
ord-91c5ad4079474305958f6bd71d3d6fff
Source dataset
uspto-grants-1990_09
Patent number
US04954163

Reaction notes

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