Hydrochloric Acid → HCID 58409088, compound

HRID 1021551Notes

Reaction equation

HRID 1021551 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]([F:12])[C:10]#[N:11].Cl.[OH-].[Na+]>C1COCC1>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]([F:12])[CH2:10][NH2:11]

Participants

5

Procedure

To a solution of 2-(2,4-dichlorophenyl)-2-fluoroacetonitrile (0.263 g, 1.29 mmol) in THF (2 ml) was added borane-DMS complex (0.134 ml, 1.42 mmol), and the reaction was heated to reflux under argon for one hour. The reaction was cooled to ambient temperature, and 0.4 ml of concentrated hydrochloric acid were added. The reaction mixture was again heated to reflux for 30 minutes, then cooled to ambient temperature and treated with 1M sodium hydroxide until the pH reached 13. The reaction was extracted three times with ether, and the combined organic layers were washed with saturated sodium chloride, dried over anhydrous potassium carbonate, filtered, and concentrated to yield 217 mg of the title compound (80.9% yield).

Workup

  1. temperaturethe reaction was heated
  2. temperatureto reflux under argon for one hour
  3. temperatureThe reaction mixture was again heated
  4. temperatureto reflux for 30 minutes
  5. temperaturecooled to ambient temperature
  6. extractionThe reaction was extracted three times with ether
  7. washthe combined organic layers were washed with saturated sodium chloride
  8. dry with materialdried over anhydrous potassium carbonate
  9. filtrationfiltered
  10. concentrationconcentrated

Sources & evidence

ORD record
ord-84580d2aaa784547be2202a629508577
Source dataset
uspto-grants-2014_05
Patent number
US08716498B2

Reaction notes

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