Potassium Carbonate → Glycine, N-(2,2-difluoroethyl)-, 1,1-dimethylethyl ester

HRID 2207104Notes

Reaction equation

HRID 2207104 reaction equation
Br[CH2:2][C:3]([O:5][C:6]([CH3:9])([CH3:8])[CH3:7])=[O:4].[F:10][CH:11]([F:14])[CH2:12][NH2:13].C(=O)([O-])[O-].[K+].[K+]>C(#N)C.CCOC(C)=O.CCCCCC>[F:10][CH:11]([F:14])[CH2:12][NH:13][CH2:2][C:3]([O:5][C:6]([CH3:9])([CH3:8])[CH3:7])=[O:4]

Participants

7

Procedure

tert-Butyl bromoacetate (2.72 g) was added to a suspension of 2,2-difluoroethylamine (1.46 g) and potassium carbonate (2.48 g) in acetonitrile (5 mL) and the mixture was stirred at RT for 24 h. The mixture was diluted with EtOAc (10 mL) and hexane (10 mL). The suspension was washed with the mixture of aqueous NaHCO3 (20 mL) and brine (10 mL). The organic extracts were dried and concentrated in vacuo to provide crude product. The crude product was purified by vacuum distillation (12 hPa, 78-80° C.) to afford sub-title compound (1.85 g) as a colourless oil; 1H NMR (300 MHz, CDCl3); 5.82 (1H, tt, J=4.4, 56 Hz), 3.45 (2H, s), 2.98 (2H, dt, J=4.4, 15.1 Hz), 1.45 (9H, s).

Workup

  1. washThe suspension was washed with the mixture of aqueous NaHCO3 (20 mL) and brine (10 mL)
  2. customThe organic extracts were dried
  3. concentrationconcentrated in vacuo
  4. customto provide crude product
  5. distillationThe crude product was purified by vacuum distillation (12 hPa, 78-80° C.)

Sources & evidence

ORD record
ord-f8533fc023044fe58804cd53b4ba5ed8
Source dataset
uspto-grants-2016_06
Patent number
US09376398B2

Reaction notes

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