Water → HCID 68429325, compound

HRID 2266889Notes

Reaction equation

HRID 2266889 reaction equation
[C-:1]#[N:2].[Na+].[F:4][C:5]([F:11])([F:10])[CH2:6][CH2:7][CH:8]=O.[C:12](=[O:15])([O-])[O-].[NH4+:16].[NH4+].[OH2:18]>>[F:4][C:5]([F:11])([F:10])[CH2:6][CH2:7][CH:8]1[NH:16][C:1](=[O:18])[NH:2][C:12]1=[O:15]

Participants

5

Conditions

Temperature
90 °C

Procedure

Sodium cyanide (4.31 g, 88.04 mmol) and 4,4,4-trifluorobutanal (3.7 g, 29.34 mmol) were added to ammonium carbonate (9.1 g, 117.4 mmol) in H2O (60 mL). The black reaction mixture was heated to 90° C. After 1 h, the mixture became homogeneous and it was stirred at 90° C. for 18 h. After cooling to 25° C., about 60 mL of solvent was removed in vacuo. Concentrated HCl (4 mL) was added to acidify the mixture to a pH of about 2 and a precipitate formed. It was filtered. The mother liquor was washed with EtOAc (3×50 mL). The organic layer was dried over MgSO4, filtered and concentrated to obtain 5-(3,3,3-trifluoropropyl)imidazolidine-2,4-dione as a brown oil (3.95 g, 69.7%). Mass Spectrum (−ESI): 195 (M−H)−.

Workup

  1. customThe black reaction mixture
  2. temperatureAfter cooling to 25° C.
  3. customabout 60 mL of solvent was removed in vacuo
  4. additionConcentrated HCl (4 mL) was added
  5. customa precipitate formed
  6. filtrationIt was filtered
  7. washThe mother liquor was washed with EtOAc (3×50 mL)
  8. dry with materialThe organic layer was dried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated

Sources & evidence

ORD record
ord-366c93c4cda04f8784809d082743c758
Source dataset
uspto-grants-2010_12
Patent number
US07858658B2

Reaction notes

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