2,4-difluorophenylethylamine 2,4-Difluorophenylacetic acid → 2-(2,4-Difluorophenyl)acetamide

HRID 1826906

Reaction equation

HRID 1826906 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][C:10]([OH:12])=O.FC(C1C=CC(F)=CC=1)C[NH2:16]>S(Cl)(Cl)=O>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][C:10]([NH2:16])=[O:12]

Participants

3

Conditions

Temperature
-78 °C

Procedure

Preparation of 2,4-difluorophenylethylamine 2,4-Difluorophenylacetic acid (5 g, 29 mmol) in thionyl chloride (50 mL) was heated at reflux for 10 min and the excess thionyl chloride removed by distillation. The acid chloride in dichloromethane (10 mL) was added to a cooled (−78° C.) solution of NH3 (20 mL) in dichloromethane (250 mL). Triethylamine (40 mL) was added and the reaction stirred at ambient temperature for 60 min. The solvents were then evaporated and the remaining solid dissolved in diethyl ether (500 mL). The organic solution was washed with 10% HCl (4×100 mL), 1 N NaOH (4×100 mL), dried over anhydrous MgSO4, filtered and concentrated to afford 630 mg (13%) of 2,4-difluorophenylacetamide.

Workup

  1. temperaturewas heated
  2. temperatureat reflux for 10 min
  3. customthe excess thionyl chloride removed by distillation
  4. additionThe acid chloride in dichloromethane (10 mL) was added to
  5. additionTriethylamine (40 mL) was added
  6. customThe solvents were then evaporated
  7. dissolutionthe remaining solid dissolved in diethyl ether (500 mL)
  8. washThe organic solution was washed with 10% HCl (4×100 mL), 1 N NaOH (4×100 mL)
  9. dry with materialdried over anhydrous MgSO4
  10. filtrationfiltered
  11. concentrationconcentrated

Sources & evidence

ORD record
ord-64189cdccc2c4c35b6ada4b983a1beaa
Source dataset
uspto-grants-2006_05
Patent number
US07053104B2

Linked notes

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