Potassium Carbonate → HCID 21938673, compound

HRID 1596655Notes

Reaction equation

HRID 1596655 reaction equation
I[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1.[Cl:9][C:10]1[CH:16]=[C:15]([F:17])[CH:14]=[C:13]([F:18])[C:11]=1[NH2:12].C(=O)([O-])[O-].[K+].[K+]>C1(C)C(C)=CC=CC=1.CCCCCCC.[Cu]>[Cl:9][C:10]1[CH:16]=[C:15]([F:17])[CH:14]=[C:13]([F:18])[C:11]=1[NH:12][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1

Participants

7

Procedure

A mixture of 4-iodotoluene (210 g, 0.96 mol), 2-chloro-4,6-difluoroaniline (204 g, 1.25 mol), copper powder (36 g, 0.57 mol), cuprous iodide (130 g, 0.68 mol), and potassium carbonate (118 g, 0.86 mol) in 500 ml of xylene is stirred vigorously and heated to reflux in a flask fitted with a Dean-Stark trap for 26 hours. After cooling to room temperature, the solids are filtered off, and the filter cake is washed with 100 ml of xylene. The solvents are evaporated under reduced pressure to give an oil which is dissolved in a mixture of 50 g of silica gel in 750 ml of heptane. The solids are filtered off and the solvents are evaporated under reduced pressure to give N-(2′-chloro-4′,6′-difluorophenyl)-4-methylaniline as an oil.

Workup

  1. temperatureheated
  2. temperatureto reflux in a flask
  3. customfitted with a Dean-Stark trap for 26 hours
  4. filtrationthe solids are filtered off
  5. washthe filter cake is washed with 100 ml of xylene
  6. customThe solvents are evaporated under reduced pressure
  7. customto give an oil which
  8. filtrationThe solids are filtered off
  9. customthe solvents are evaporated under reduced pressure

Sources & evidence

ORD record
ord-99e443cb45d44e899acc1a519a93457a
Source dataset
uspto-grants-2001_09
Patent number
US06291523B1

Reaction notes

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