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

HRID 2373629Notes

Reaction equation

HRID 2373629 reaction equation
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

Participants

7

Conditions

Temperature
100 °C

Procedure

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).

Workup

  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)

Sources & evidence

ORD record
ord-403cbcf1264c4b8eb00f0a683d3a6370
Source dataset
uspto-grants-2008_12
Patent number
US07459456B2

Reaction notes

Loading…