Ethyl trifluoroacetate → HCID 15613830, compound

HRID 253215Notes

Reaction equation

HRID 253215 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][C:12]#[N:13])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[F:14][C:15]([F:22])([F:21])[C:16](OCC)=[O:17].[O-]CC.[Na+]>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]([C:16](=[O:17])[C:15]([F:22])([F:21])[F:14])[C:12]#[N:13])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]

Participants

5

Procedure

To a mixture of [3,4-bis(methyloxy)phenyl]acetonitrile (2.0 g, 11 mmol) and ethyl trifluoroacetate (1.7 mL, 14 mmol) in ethanol (4 mL) was added a sodium ethoxide solution (21%, 8.4 mL, 23 mmol), and the resulting mixture was heated at reflux for 18 hours. After cooling to room temperature, it was poured into a mixture of ice-water (50 mL). This aqueous mixture was washed with dichloromethane (3×20 mL) then acidified to pH 1. The acidified mixture was extracted with ethyl acetate (3×30 mL). The combined extract was washed with aqueous sodium bicarbonate solution, brine, dried over sodium sulfate, filtered and concentrated to give 2-[3,4-bis(methyloxy)phenyl]-4,4,4-trifluoro-3-oxobutanenitrile as a brown oil (0.8 g, 3.4 mmol, 30% yield), MS (EI) for C12H10F3NO3: 274 (MH+).

Workup

  1. temperaturethe resulting mixture was heated
  2. temperatureat reflux for 18 hours
  3. washThis aqueous mixture was washed with dichloromethane (3×20 mL)
  4. extractionThe acidified mixture was extracted with ethyl acetate (3×30 mL)
  5. extractionThe combined extract
  6. washwas washed with aqueous sodium bicarbonate solution, brine
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-ab5f809651b8402b9dfdc4e931f106a8
Source dataset
uspto-grants-2011_01
Patent number
US07872014B2

Reaction notes

Loading…