Reaktion #158235

ord-450a6a6d07304294b12c5a36314c2901

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added
  2. 2
    ExtraktionThe aqueous layer was extracted with Et2O (50 mL, 3 times)
  3. 3
    Trocknendried over Na2SO4
  4. 4
    Einengenconcentrated
  5. 5
    workup.ADDITIONTo the concentrated sample, hexane was added
  6. 6
    Sonstigethe resulting precipitate was isolated

Vorschrift

To a solution of 1,2-diiodo-4,5-dimethoxy-3-methylbenzene (Example 5(b), 2.0 g, 4.95 mmol) in 120 mL of a mixture of THF and Et2O (1:1) was added dropwise at −78° C., isopropylmagnesium chloride (2 M in THF, 2.72 mL, 5.44 mmol). After the mixture was stirred for 2 h at that temperature, B(OiPr)3 (10.50 ml, 14.84 mmol) was added. The solution was warmed to room temperature overnight; then a saturated solution of NH4Cl was added, and the resulting mixture was stirred for 30 min at room temperature. The aqueous layer was extracted with Et2O (50 mL, 3 times), dried over Na2SO4 and concentrated. To the concentrated sample, hexane was added and the resulting precipitate was isolated to give 0.90 g of the pure product (56%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08822720B2uspto-grants-2014_09