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Tetrahydrofuran → (S)-4-(pyridin-2-yl)oxazolidin-2-one

HRID 539128
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HRID 539128 반응식
Cl.Cl.[NH2:3][C@@H:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=1)[CH2:5][OH:6].[OH-].[K+].C1C[O:18][CH2:17]C1.C(=O)(OC(Cl)(Cl)Cl)OC(Cl)(Cl)Cl>O.CCOC(C)=O>[N:8]1[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=1[C@H:4]1[CH2:5][O:6][C:17](=[O:18])[NH:3]1
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참가 물질

7

반응물 4

HCID 8028TetrahydrofuranHCID 14797Potassium HydroxideHCID 94429TriphosgeneHCID 67033506(S)-2-Amino-2-(pyridin-2-yl)ethanol dihydrochloride

생성물 1

HCID 10964848(S)-4-(pyridin-2-yl)oxazolidin-2-one수율 21%

시약·촉매·용매 2

HCID 962Water
용매
HCID 8857Ethyl Acetate용매

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온도
0 °C

실험 절차

To a solution of (S)-2-amino-2-(pyridin-2-yl)ethanol bis hydrochloride (0.80 g, 5.8 mmol) in water (50 mL) cooled to 0° C. was added potassium hydroxide (2.6 g, 46 mmol) and the reaction stirred at 0° C. for 15 minutes, followed by the addition of THF (100 mL) and the reaction cooled to 0° C. To the reaction was next added bis(trichloromethyl) carbonate (1.7 g, 5.8 mmol) and the reaction stirred at 0° C. for 2 hours. The reaction was diluted with EtOAc (300 mL) and the layers were separated. The organic layer was washed with water (100 mL) and brine (100 mL), dried over MgSO4 and concentrated in vacuo. The crude material was chromatographed using EtOAc as eluent to yield (S)-4-(pyridin-2-yl)oxazolidin-2-one (0.20 g, 21%).

후처리

  1. temperaturethe reaction cooled to 0° C
  2. stirringthe reaction stirred at 0° C. for 2 hours
  3. customthe layers were separated
  4. washThe organic layer was washed with water (100 mL) and brine (100 mL)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customThe crude material was chromatographed

출처 및 근거

ORD 기록
ord-3902f1ff570e4d09a7721bbedeef7b92
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08865726B2

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