Reaktion #352659

ord-dbaa7b0e138049c0ba1be899d7c03be3

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturat reflux for 3 hours
  3. 3
    workup.WAITleft
  4. 4
    SonstigeThe solvent of the reaction was removed on a rotary evaporator
  5. 5
    Extraktionthe crude solid was extracted into methylene chloride (500 ml)
  6. 6
    FiltrationThe insolubles were filtered off
  7. 7
    EinengenThe dichloromethane solution was concentrated
  8. 8
    Sonstigethe material was purified on a flash chromatography column (SiO2, 105 g
  9. 9
    Wascheneluted with 2:3 dichloromethane
  10. 10
    SonstigeThe desired product thus purified
  11. 11
    SonstigeRecrystallization twice from ethanol

Vorschrift

A mixture of 4-hydroxy-3-methoxybenzonitrile (7.5 g, 50 mmol), K2CO3 (12.5 g), and 1,3-dibromopropane (15 g, 75 mmol) in acetonitrile (100 ml) was heated at reflux for 3 hours and left standing at room temperature overnight. The solvent of the reaction was removed on a rotary evaporator, and the crude solid was extracted into methylene chloride (500 ml). The insolubles were filtered off. The dichloromethane solution was concentrated and the material was purified on a flash chromatography column (SiO2, 105 g; eluted with 2:3 dichloromethane:hexane, and then with dichloromethane). The desired product thus purified weighed 7.74 g (52%). Recrystallization twice from ethanol gave analytically pure 4-(3-bromopropoxy)-3-methoxybenzonitrile, m.p.=99°-101° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05648363uspto-grants-1997_07