Reaktion #570650

ord-ea6bf6b283f04a6b8ca4c0ca02845c2f

Reaktionsgleichung

C1COC1
Oxetane
[Cl-].[NH4+]
NH4Cl
Fc1ccc(Br)cc1
4-bromo-1-fluorobenzene
[Mg]
magnesium
II
iodine
OCCCc1ccc(F)cc1
title compound
Ausbeute 51.6%
OCCCc1ccc(F)cc1
4-Fluorobenzenepropanol
Ausbeute 51.6%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe reaction mixture was heated
  2. 2
    Temperaturat reflux overnight
  3. 3
    Extraktionextracted with ER (2×150 ml)
  4. 4
    Trocknendried (Na2SO4) extracts
  5. 5
    Sonstigewere evaporated
  6. 6
    SonstigeThe residual oil was purified by flash chromatography over silica gel (Merck 9285, 5.0 cm wide column)
  7. 7
    Wascheneluting with ER-CX (1:5→1:3)
  8. 8
    workup.DISTILLATIONThe resultant oil was further purified by distillation

Vorschrift

A Grignard reagent was prepared from 4-bromo-1-fluorobenzene (8.0 g), magnesium turnings (1.10 g), and iodine (one small crystal) in THF (40 ml). Oxetane (2.3 g) in THF (10 ml) was added at RT and the reaction mixture was heated at reflux overnight. The cooled solution was poured into aqueous saturated NH4Cl (100 ml), extracted with ER (2×150 ml) and the combined, dried (Na2SO4) extracts were evaporated. The residual oil was purified by flash chromatography over silica gel (Merck 9285, 5.0 cm wide column), eluting with ER-CX (1:5→1:3). The resultant oil was further purified by distillation to give the title compound (3.15 g) as a colourless oil, b.p. 150°/0.8 torr.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05225445uspto-grants-1993_07