Reaktion #46780

ord-574c4a03c68d4feba70665e423d45be3

Reaktionsgleichung

[Cl-].[NH4+]
NH4Cl
C=[C](C)[Mg][Br]
isopropenylmagnesium bromide
O=[N+]([O-])c1ccccc1F
2-fluoronitrobenzene
Cc1cc2cccc(F)c2[nH]1
expected compound
Cc1cc2cccc(F)c2[nH]1
7-Fluoro-2-methyl-1H-indole

Lösungsmittel

Reaktionsbedingungen

Temperatur
-20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITthe mixture is left
  2. 2
    Extraktionthe aqueous phase is extracted with ether
  3. 3
    Einengenthe combined organic phases are concentrated under vacuum
  4. 4
    Extraktionextracted with DCM
  5. 5
    Waschenthe organic phase is washed with water and with a saturated NaCl solution
  6. 6
    Trocknendried over MgSO4
  7. 7
    Sonstigethe solvent is evaporated under vacuum
  8. 8
    SonstigeThe residue is chromatographed on silica gel, elution

Vorschrift

1600 ml of a 0.5M solution of isopropenylmagnesium bromide in THF are cooled to −25° C. under an argon atmosphere, a solution of 37.65 g of 2-fluoronitrobenzene in 250 ml of THF is then added dropwise and the mixture is left stirring at −20° C. for 1 hour. The reaction mixture is poured into a saturated NH4Cl solution, the aqueous phase is extracted with ether and the combined organic phases are concentrated under vacuum. The residue is taken up in water and extracted with DCM, the organic phase is washed with water and with a saturated NaCl solution and dried over MgSO4, and the solvent is evaporated under vacuum. The residue is chromatographed on silica gel, elution being carried out with a cyclohexane/EtOAc mixture (95/5; v/v). 12.35 g of the expected compound are obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741363B2uspto-grants-2010_06