Reaktion #337359

ord-d4fc6c06ddbf4eef95afc69037754b35

Reaktionsgleichung

CCOC(=O)c1ccc(Br)cc1
ethyl 4-bromobenzoate
C[CH2][Mg][Br]
ethylmagnesium bromide
CCOCC
Et2O
CCC(O)(CC)c1ccc(Br)cc1
3-(4-bromophenyl)-pentan-3-ol

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe reaction mixture was removed from the ice-bath
  2. 2
    SonstigeAfter 18 h the opaque mixture was quenched with satd ammonium chloride (50 mL)
  3. 3
    Extraktionextracted with Et2O (2×50 mL)
  4. 4
    WaschenThe combined extracts were washed with brine
  5. 5
    Trocknendried (anhyd Na2SO4)
  6. 6
    Einengenconcentrated under reduced pressure

Vorschrift

A solution of ethyl 4-bromobenzoate (1.6 mL, 10 mmol) in anhyd THF (50 mL) was chilled to 0° C. and then charged dropwise with a 3.0 M solution of ethylmagnesium bromide in Et2O (7.0 mL, 21 mmol). After 15 min, the reaction mixture was removed from the ice-bath and stirred at ambient temperature. After 18 h the opaque mixture was quenched with satd ammonium chloride (50 mL) and extracted with Et2O (2×50 mL). The combined extracts were washed with brine, dried (anhyd Na2SO4) and concentrated under reduced pressure to give 3-(4-bromophenyl)-pentan-3-ol (2.45 g, quant) as a colorless liquid, which was used without purification in the next step: 1H-NMR (CDCl3) δ 7.46 (2H, d, J=8.3), 7.26 (2.3H, d, J=8.3), 1.78-1.86 (4H, overlapping quartets, J=7), 0.76 (6H, t, J=7.3).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07863298B2uspto-grants-2011_01