Reaktion #584025

ord-7db84a3d08534c3d82cb27ed658b0b38

Reaktionsgleichung

Brc1cccc(Br)c1
1,3-dibromobenzene
CN(C)C=O
N,N-dimethylformamide
[Li][CH2]CCC
n-butyllithium
CCC[CH2][Mg][Cl]
n-Butylmagnesium chloride
O=Cc1cccc(Br)c1
title compound
Ausbeute 78.2%
O=Cc1cccc(Br)c1
3-bromobenzaldehyde
Ausbeute 78.2%

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto give a suspension
  2. 2
    Sonstigethe temperature below 5° C.
  3. 3
    workup.WAITover a period of 15 minutes
  4. 4
    Sonstigeto give a suspension
  5. 5
    workup.STIRRINGThe suspension was stirred at 0° C. for 5 hours
  6. 6
    ExtraktionThe reaction mixture was extracted twice with toluene (20 mL)
  7. 7
    Waschenwashed with water (20 mL)
  8. 8
    Trocknendried over magnesium sulfate
  9. 9
    workup.ADDITIONToluene was added to the solution to a volume of 85 mL
  10. 10
    SonstigeThe solution (83 ml) was purified by flash column chromatography on silica gel in a developing solvent system of hexane-ethyl acetate (25:1

Vorschrift

n-Butylmagnesium chloride (4.00 mmol) in 2.00M tetrahydrofuran solution (2.00 mL) was added to ice-cooled n-butyllithium (8.06 mmol) in 1.55M hexane (5.20 mL). The mixture was stirred at 0° C. for 15 minutes to give a suspension. To the suspension was added dropwise a toluene solution (25 mL) containing 1,3-dibromobenzene (2.36 g, 10.0 mmol), while keeping the temperature below 5° C., over a period of 15 minutes, thereby to give a suspension. The suspension was stirred at 0° C. for 5 hours, and then N,N-dimethylformamide (1.0 mL, 13 mmol) was added thereto. The resultant mixture was stirred at 0° C. for 30 minutes, and 10% aqueous acetic acid (20 mL) was added. The reaction mixture was extracted twice with toluene (20 mL). The organic extracts were combined, washed with water (20 mL), and dried over magnesium sulfate. Toluene was added to the solution to a volume of 85 mL. The solution (83 ml) was purified by flash column chromatography on silica gel in a developing solvent system of hexane-ethyl acetate (25:1, v/v) to give the title compound (1.446 g, 78% yield) as a pale yellowish crystalline solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06946559B2uspto-grants-2005_09