Reaktion #356647

ord-2cc2ba8275514663bbff76424205c0ef

Reaktionsgleichung

Cc1cc(C)[c]([Mg][Br])c(C)c1
mesitylmagnesium bromide
CC(C)(C)P(C(C)(C)C)C(C)(C)C
PtBu3
BrC1=Cc2ccccc2C1
2-bromo-1H-indene
Cc1cc(C)c(C2=Cc3ccccc3C2)c(C)c1
2-Mesityl-1H-indene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe organic layer was separated
  2. 2
    Extraktionthe aqueous layer was extracted with 3×100 ml of ether
  3. 3
    TrocknenThe combined organic fractions were dried over K2CO3
  4. 4
    Sonstigeevaporated to dryness
  5. 5
    SonstigeThe product was isolated by flash chromatography on Silica Gel 60 (40-63 um, d 30 mm, l 300 mm, eluent: hexanes-dichloromethane, 20:1, vol.)

Vorschrift

A mixture of 50.0 ml (20.0 mmol) of 0.4 M mesitylmagnesium bromide in THF, 230 mg (0.40 mmol) of Pd(dba)2, 162 mg (0.80 mmol) of PtBu3, and 3.90 g (20.0 mmol) of 2-bromo-1H-indene was stirred for 48 h at ambient temperature. Then, to the resulting mixture 200 ml of brine was added. The organic layer was separated, and the aqueous layer was extracted with 3×100 ml of ether. The combined organic fractions were dried over K2CO3 and then evaporated to dryness. The product was isolated by flash chromatography on Silica Gel 60 (40-63 um, d 30 mm, l 300 mm, eluent: hexanes-dichloromethane, 20:1, vol.). Yield 3.19 g (68%) of white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07446216B2uspto-grants-2008_11