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

HRID 2207104
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HRID 2207104 반응식
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]
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참가 물질

7

반응물 3

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

생성물 1

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

시약·촉매·용매 3

HCID 6342Acetonitrile용매HCID 8058Hexane용매
HCID 8857
Ethyl Acetate
용매

실험 절차

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).

후처리

  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.)

출처 및 근거

ORD 기록
ord-f8533fc023044fe58804cd53b4ba5ed8
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09376398B2

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