Ammonia → HCID 53629170, compound

HRID 1926780Notes

Reaction equation

HRID 1926780 reaction equation
C([N:8]1[CH2:12][CH:11]([CH2:13][C:14]([F:17])([F:16])[F:15])[CH2:10][C:9]1=[O:18])C1C=CC=CC=1.N.[Na].[Cl-].[NH4+]>C(OCC)C.C(O)C.C(O)(C)(C)C>[F:17][C:14]([F:15])([F:16])[CH2:13][CH:11]1[CH2:12][NH:8][C:9](=[O:18])[CH2:10]1

Participants

8

Conditions

Temperature
-78 °C

Procedure

1-Benzyl-4-(2,2,2-trifluoroethyl)pyrrolidin-2-one x102 (1.67 g, 6.5 mmol) is dissolved in diethyl ether (17 ml) and anhydrous tert-butanol (7 ml). The solution is cooled to −78° C. and ammonia (33 ml) is condensed into the flask. Sodium (0.373 g, 16.2 mmol) is added to the solution portionwise at −78° C., followed by the anhydrous tert-butanol (7 ml). The reaction mixture is stirred at −78° C. for 2-3 h. Ethanol (50 ml) is slowly added. The mixture is warmed to room temperature and stirred overnight. Saturated ammonium chloride is added and the mixture is extracted with ether (3 times). The organic layers are combined, dried over magnesium sulphate, filtered and concentrated in vacuo to obtain 4-(2,2,2-trifluoroethyl)pyrrolidin-2-one x103 as an orange solid (0.61 g).

Workup

  1. customcondensed into the flask
  2. temperatureThe mixture is warmed to room temperature
  3. stirringstirred overnight
  4. extractionthe mixture is extracted with ether (3 times)
  5. dry with materialdried over magnesium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-12b2441e72fd4e9b985e62c76415179e
Source dataset
uspto-grants-2012_05
Patent number
US08183241B2

Reaction notes

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