تفاعل #46780

ord-574c4a03c68d4feba70665e423d45be3

معادلة التفاعل

[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

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
-20°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITthe mixture is left
  2. 2
    استخلاصthe aqueous phase is extracted with ether
  3. 3
    تركيزthe combined organic phases are concentrated under vacuum
  4. 4
    استخلاصextracted with DCM
  5. 5
    غسيلthe organic phase is washed with water and with a saturated NaCl solution
  6. 6
    تجفيفdried over MgSO4
  7. 7
    أخرىthe solvent is evaporated under vacuum
  8. 8
    أخرىThe residue is chromatographed on silica gel, elution

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07741363B2uspto-grants-2010_06