Réaction #12063

ord-c95ea336c63e4d4ea8961bed6584d030

Équation de réaction

Fc1ccc(CCl)cc1
4-fluorophenylmethyl chloride
[Mg]
magnesium
BrC1=Cc2ccccc2C1
2-bromo-indene
[Cl-]
chloride
Fc1ccc(CC2=Cc3ccccc3C2)cc1
2-(4-fluorophenylmethyl)indene

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe system was carefully heated
  2. 2
    Autreafter initiation of the reaction
  3. 3
    Températurewhile maintain a gentle reflux
  4. 4
    TempératureAfter refluxing for 1.5 hours
  5. 5
    Températurethe Grignard solution was cooled
  6. 6
    TempératureThe system was gently heated
  7. 7
    Températureto reflux overnight
  8. 8
    Températurecooled
  9. 9
    Autrequenched
  10. 10
    workup.ADDITIONby adding 150 mL of 1.0 M aqueous hydrochloric acid
  11. 11
    AutreThe product was isolated
  12. 12
    Autrepurified (hexanes/silica) as for 2-benzyl-indene

Mode opératoire

To a suspension of freshly ground magnesium (0.58 g, 23 mmol) in 100 mL of ether was added about 3 mL of a 15 mL ether solution containing 3.0 g (21 mmol) of 4-fluorophenylmethyl chloride. The system was carefully heated and after initiation of the reaction, the remaining chloride solution added over 30 minutes while maintain a gentle reflux. After refluxing for 1.5 hours, the Grignard solution was cooled and cannulated to a mixture of 3.65 g (19 mmol) of 2-bromo-indene, 150 mg (0.20 mmol) of NiCl2(dppp) and 100 mL of ether. The system was gently heated to reflux overnight and then cooled and quenched by adding 150 mL of 1.0 M aqueous hydrochloric acid. The product was isolated and purified (hexanes/silica) as for 2-benzyl-indene. Yield: 3.45 g, 74 percent

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07098356B2uspto-grants-2006_08