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Potassium Carbonate → Tert-butyl 2-[(2,2-difluoroethyl)amino]acetate

HRID 2207104
Notes
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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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

HCID 11430Potassium CarbonateHCID 79177tert-Butyl bromoacetateHCID 1362742,2-Difluoroethanamine

Product 1

HCID 89906572Tert-butyl 2-[(2,2-difluoroethyl)amino]acetateYield 68%

Reagents, catalysts & solvents 3

HCID 6342AcetonitrileSolvent
HCID 8058
Hexane
Solvent
HCID 8857Ethyl AcetateSolvent

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
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09376398B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes