Réaction #452426

ord-9b1f852a20544f969f0f2f8380e9970a

Équation de réaction

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
Rendement 26.0%
CC(C)n1cc(CCO)cn1
2-(1-isopropyl-1H-pyrazol-4-yl)-1-ethanol
Rendement 26.0%

Conditions de réaction

Température
100°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction mixture was then cooled to ambient and
  2. 2
    Concentrationthen concentrated under reduced pressure
  3. 3
    AutreThe residue was partitioned between water and dichloromethane
  4. 4
    LavageThe organic phase was then washed with water
  5. 5
    Séchagewas then dried over sodium sulfate
  6. 6
    ConcentrationThe remaining organics were concentrated under reduced pressure

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06126932uspto-grants-2000_10