Reaktion #452426

ord-9b1f852a20544f969f0f2f8380e9970a

Reaktionsgleichung

CC(C)I
2-iodopropane
OCCc1cn[nH]c1
2-(4-pyrazolyl)-1-ethanol
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CC(C)n1cc(CCO)cn1
title compound
Ausbeute 26.0%
CC(C)n1cc(CCO)cn1
2-(1-isopropyl-1H-pyrazol-4-yl)-1-ethanol
Ausbeute 26.0%

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was then cooled to ambient and
  2. 2
    Einengenthen concentrated under reduced pressure
  3. 3
    SonstigeThe residue was partitioned between water and dichloromethane
  4. 4
    WaschenThe organic phase was then washed with water
  5. 5
    Trocknenwas then dried over sodium sulfate
  6. 6
    EinengenThe remaining organics were concentrated under reduced pressure

Vorschrift

To a solution of 1.0 gm (9.0 mMol) 2-(4-pyrazolyl)-1-ethanol in 36 mL dimethylformamide were added 2.38 gm (22.5 mMol) sodium carbonate followed by the dropwise addition of a solution of 0.89 mL (9.0 mMol) 2-iodopropane in 8 mL dimethylformamide. The reaction mixture was heated to 100° C. for 18 hours. The reaction mixture was then cooled to ambient and then concentrated under reduced pressure. The residue was partitioned between water and dichloromethane. The organic phase was then washed with water followed by saturated aqueous sodium chloride and was then dried over sodium sulfate. The remaining organics were concentrated under reduced pressure to give 0.36 gm (26.0%) of the title compound as a brown oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06126932uspto-grants-2000_10