N,N'-Dimethylethylenediamine → 3-[3-(2-Hydroxyethyl)phenyl]-1,3-oxazolidin-2-one

HRID 15857

反応式

HRID 15857 の反応式
Br[C:2]1[CH:3]=[C:4]([CH2:8][CH2:9][OH:10])[CH:5]=[CH:6][CH:7]=1.C[NH:12][CH2:13][CH2:14]NC.[C:17](=[O:20])([O-])[O-:18].[K+].[K+].[Cl-].[NH4+]>O1CCOCC1.[Cu]I>[OH:10][CH2:9][CH2:8][C:4]1[CH:3]=[C:2]([N:12]2[CH2:13][CH2:14][O:18][C:17]2=[O:20])[CH:7]=[CH:6][CH:5]=1

参加物

7

反応条件

温度
100 °C

実験手順

A solution 2-(3-bromophenyl)ethanol (1.00 g, 5.00 mmol), 2-oxazolidin-2-one (874 mg, 10.04 mmol), copper(I)iodide (96 mg, 0.50 mmol), N,N′-dimethyl-1,2-ethanediamine (60 μL, 49 mg, 0.56 mmol) and potassium carbonate (1.04 g, 7.50 mmol) were suspended in dioxane (6 mL). The mixture was stirred under nitrogen for 2.5 h at 100° C. After addition of copper(I)iodide (96 mg, 0.50 mmol) and N,N′-dimethyl-1,2-ethanediamine (60 μl, 49 mg, 0.56 mmol) stirring was continued for another 2 h at 100° C. After cooling down to room temperature, the mixture was poured into saturated aqueous ammonium chloride solution and extracted with dichloromethane. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The crude compound was purified by flash chromatography on silica gel, eluting with ethyl acetate-cyclohexane (1:1 to 1:0) affording the title compound in 64% yield (664 mg).

後処理

  1. stirringstirring
  2. waitwas continued for another 2 h at 100° C
  3. temperatureAfter cooling down to room temperature
  4. extractionextracted with dichloromethane
  5. dry with materialThe organic layer was dried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe crude compound was purified by flash chromatography on silica gel
  8. washeluting with ethyl acetate-cyclohexane (1:1 to 1:0)

出典と根拠

ORDレコード
ord-3e987077da3849439d683577127ec598
出典データセット
uspto-grants-2010_06
特許番号
US07732600B2

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