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

HRID 539128
ノート
印刷プレビュー

反応式

HRID 539128 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
0 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-3902f1ff570e4d09a7721bbedeef7b92
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08865726B2

反応ノート

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