Sodium Hydroxide → 4-Chloro-5-methoxy-2-methylaniline

HRID 2410004Notes

Reaction equation

HRID 2410004 reaction equation
[Cl:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([NH:10]C(=O)C(F)(F)F)=[C:4]([CH3:17])[CH:3]=1.[OH-].[Na+]>C(O)C>[Cl:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([NH2:10])=[C:4]([CH3:17])[CH:3]=1

Participants

4

Conditions

Temperature
80 °C

Procedure

To a suspension of N-(4-chloro-5-methoxy-2-methylphenyl)-2,2,2-trifluoroacetamide (7.02 g) in ethanol (50 mL) was added 2 mol/L aqueous sodium hydroxide solution at room temperature, and the mixture was stirred at external temperature of 80° C. for 30 minutes. The reaction mixture was left to be cooled and concentrated under reduced pressure. To the residue was added water, and the mixture was stirred for 1 hour. The precipitate was collected by filtration, washed with water, and then dried under reduced pressure to obtain the title compound (4.15 g). 1H-NMR (CDCl3) δ ppm: 2.08 (3H, s), 3.40-3.82 (2H, br), 3.83 (3H, s), 6.29 (1H, s), 6.99-7.04 (1H, m).

Workup

  1. waitThe reaction mixture was left
  2. temperatureto be cooled
  3. concentrationconcentrated under reduced pressure
  4. additionTo the residue was added water
  5. stirringthe mixture was stirred for 1 hour
  6. filtrationThe precipitate was collected by filtration
  7. washwashed with water
  8. customdried under reduced pressure

Sources & evidence

ORD record
ord-cae6b7d63ea1418a8239585d8711e42b
Source dataset
uspto-grants-2014_08
Patent number
US08815903B2

Reaction notes

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