Réaction #2329009

ord-b67df847835e4f2289cb05b55d61b33d

Équation de réaction

C[C@@H]1CCC[C@H]1O
Trans-2-Methylcylopentanol
N#Cc1ccc(F)cc1C(F)(F)F
2-Trifluoromethyl-4-fluoro-benzonitrile
O
water
C[C@@H]1CCC[C@H]1Oc1ccc(C#N)c(C(F)(F)F)c1
4-(trans-2-Methyl-cyclopentyloxy)-2-trifluoromethyl-benzonitrile
Rendement 83.2%

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Séchagedried round bottom flask under nitrogen containing 0.5 mL of dry tetrahydrofuran (“THF”)
  2. 2
    workup.ADDITIONA 1.0 M solution of potassium t-butoxide in t-butanol (0.5 mL) was added dropwise
  3. 3
    AutreThe above solution was then transferred via syringe to a flask
  4. 4
    workup.STIRRINGThe mixture was stirred at 0° C. for 3 h
  5. 5
    Températurewarmed to room temperature
  6. 6
    workup.STIRRINGstirred for 16 h
  7. 7
    TempératureThe reaction mixture was then cooled to 0° C.
  8. 8
    workup.ADDITIONpoured into a seperatory funnel
  9. 9
    Extractionextracted with 10 mL of methyl tert-butyl ether
  10. 10
    LavageThe organic phase was washed with water, brine
  11. 11
    Séchagedried (MgSO4)
  12. 12
    Concentrationconcentrated in vacuo
  13. 13
    Autrethe residue purified by reverse phase HPLC (Shimadzu)

Mode opératoire

Trans-2-Methylcylopentanol (50 mg, 0.5 mmol) was added to a flame dried round bottom flask under nitrogen containing 0.5 mL of dry tetrahydrofuran (“THF”) and cooled to 0° C. A 1.0 M solution of potassium t-butoxide in t-butanol (0.5 mL) was added dropwise and the reaction mixture stirred at 0° C. for 0.5 h. The above solution was then transferred via syringe to a flask containing 2-Trifluoromethyl-4-fluoro-benzonitrile (95 mg, 0.5 mmol) in 0.5 mL of THF at 0° C. The mixture was stirred at 0° C. for 3 h, warmed to room temperature and stirred for 16 h. The reaction mixture was then cooled to 0° C., poured into a seperatory funnel containing 8 mL of water, and extracted with 10 mL of methyl tert-butyl ether. The organic phase was washed with water, brine, dried (MgSO4), concentrated in vacuo, and the residue purified by reverse phase HPLC (Shimadzu) to give 112 mg 4-(trans-2-Methyl-cyclopentyloxy)-2-trifluoromethyl-benzonitrile. GC/MS: 269 (M/Z for C14H14F3NO).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07670613B2uspto-grants-2010_03