Reaktion #3870

ord-62c89f061fa24da181f2e8c2e39d52b5

Reaktionsgleichung

COc1cccc2c1OC(C)(C)C2N1CCCCC1
7-Methoxy-3-piperidino-2,2-dimethylbenzofuran
Br
HBr
CC1(C)Oc2c(O)cccc2C1N1CCCCC1
desired product
CC1(C)Oc2c(O)cccc2C1N1CCCCC1
7-Hydroxy-3-piperidino-2,2-dimethylbenzofuran

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe solution refluxed for 3 hours
  2. 2
    workup.ADDITIONThe reaction mixture is poured
  3. 3
    SonstigeThe alkaline reaction mixture
  4. 4
    Extraktionis extracted with methylene chloride
  5. 5
    Waschenthe organic phase washed with water
  6. 6
    Sonstigedried
  7. 7
    Filtrationfiltered
  8. 8
    Sonstigeevaporated in vacuo
  9. 9
    SonstigeThe residue is chromatographed on silica gel eluting with ethyl acetate/hexane (1:3)

Vorschrift

7-Methoxy-3-piperidino-2,2-dimethylbenzofuran (65.1 g) is added to a stirred mixture of glacial acetic acid (340 ml) and 48% HBr (340 ml) and the solution refluxed for 3 hours. The reaction mixture is poured into crushed ice/H2O and brought to a pH=8-10. The alkaline reaction mixture is extracted with methylene chloride and the organic phase washed with water, dried, filtered and evaporated in vacuo. The residue is chromatographed on silica gel eluting with ethyl acetate/hexane (1:3) affording the desired product as a liquid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04722925uspto-grants-1988_02