تفاعل #83149

ord-ccc751841a9b4b238bdcd8e8f959367b

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىto form a solution
  2. 2
    workup.STIRRINGunder stirring at room temperature
  3. 3
    workup.STIRRINGby stirring for 30 minutes on an oil bath
  4. 4
    أخرىkept at about 70° C
  5. 5
    أخرىAfter the reaction
  6. 6
    أخرىto precipitate a crystal
  7. 7
    ترشيحThe crystal was recovered by filtration
  8. 8
    غسيلwashed with water
  9. 9
    أخرىfollowed by purification by silica gel column chromatography (eluent: toluene/ethyl acetate =100/1) and recrystallization from a toluene-methanol mixture solvent

الإجراء التجريبي

Then, 0.30 g (1.18 mM) of (5R)-3-(4-hydroxyphenyl)-5-phenyl-2-oxazolidinone and 4.6 ml of DMF were placed in 30 ml-round bottomed flask, followed by stirring to form a solution. To the solution, 0.053 g (1.33 mM) of 60%-oily sodium hydride was added under stirring at room temperature. After the settlement of foaming, 0.25 ml (1.38 mM) of 1-iodooctane was added to the mixture, followed by stirring for 30 minutes on an oil bath kept at about 70° C. After the reaction, the reaction mixture was poured into ice water to precipitate a crystal. The crystal was recovered by filtration and washed with water, followed by purification by silica gel column chromatography (eluent: toluene/ethyl acetate =100/1) and recrystallization from a toluene-methanol mixture solvent to obtain 0.13 g of (5R)-3-(4-octyloxyphenyl)-5-phenyl-2-oxazolidinone (Yield: 30.1%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05624600uspto-grants-1997_04