반응 #46780

ord-574c4a03c68d4feba70665e423d45be3

반응 방정식

[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

용매

반응 조건

온도
-20°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITthe mixture is left
  2. 2
    추출the aqueous phase is extracted with ether
  3. 3
    농축the combined organic phases are concentrated under vacuum
  4. 4
    추출extracted with DCM
  5. 5
    세척the organic phase is washed with water and with a saturated NaCl solution
  6. 6
    건조dried over MgSO4
  7. 7
    기타the solvent is evaporated under vacuum
  8. 8
    기타The residue is chromatographed on silica gel, elution

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741363B2uspto-grants-2010_06