Reaktion #43280

ord-d5f8ba010fcf42e49e299046f5d44489

Reaktionsgleichung

CCOCC
ether
O=Cc1ccc(Br)cc1
4-bromobenzaldehyde
C1CCOC1
THF
CCCCCC(O)c1ccc(Br)cc1
4
Ausbeute 76.0%
CCCCCC(O)c1ccc(Br)cc1
1-(4-Bromo-phenyl)-hexan-1-ol
Ausbeute 76.0%

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe reaction was quenched by addition of 200 mL saturated ammonium chloride solution
  2. 2
    ExtraktionThe resulting mixture was extracted with ethyl acetate (3×100 mL)
  3. 3
    Trocknenthe combined ethyl acetate solution was dried (Na2SO4)
  4. 4
    Filtrationfiltered
  5. 5
    Sonstigeevaporated
  6. 6
    SonstigePurification of the residue by flash chromatography on silica gel

Vorschrift

n-PentylMgBr (29 mL, 58 mmol, 2 M/ether) was added to a 0° C. solution of 4-bromobenzaldehyde (9.953 g, 54 mmol) in THF (100 mL). After 1 h, the reaction was quenched by addition of 200 mL saturated ammonium chloride solution. The resulting mixture was extracted with ethyl acetate (3×100 mL) and the combined ethyl acetate solution was dried (Na2SO4), filtered and evaporated. Purification of the residue by flash chromatography on silica gel gave 4 (10.501 g, 76%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732443B2uspto-grants-2010_06