Reaktion #3869

ord-29d226711096432384d0866c11b1dd4d

Reaktionsgleichung

C1CCNCC1
piperidine
COc1cccc2c1OC(C)(C)C2O
product
COc1cccc2c1OC(C)(C)C2O
7-Methoxy-3-hydroxy-2,2-dimethylbenzofuran
O=C([O-])O.[Na+]
sodium bicarbonate
CS(=O)(=O)Cl
Methanesulfonyl chloride
COc1cccc2c1OC(C)(C)C2N1CCCCC1
desired product
COc1cccc2c1OC(C)(C)C2N1CCCCC1
7-Methoxy-3-piperidino-2,2-dimethylbenzofuran

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeat RT
  2. 2
    Temperaturcooled to 0° C.
  3. 3
    workup.STIRRINGstirring
  4. 4
    workup.WAITcontinued at RT overnight
  5. 5
    Sonstigethe phases separated
  6. 6
    Waschenthe organic phase washed with sodium bicarbonate
  7. 7
    Sonstigedried
  8. 8
    Filtrationfiltered
  9. 9
    Sonstigeevaporated in vacuo
  10. 10
    workup.DISSOLUTIONThe residue is dissolved in toluene
  11. 11
    Sonstigeevaporated in vacuo

Vorschrift

Triethylamine (29 ml) is added to a stirred solution of the product obtained in Step 4. (25.4 g) in methylene chloride (560 ml) at RT under nitrogen. Methanesulfonyl chloride (11.1 ml) is added dropwise to the mixture which is cooled to 0° C. The mixture is stirred for 3 hours at RT, cooled to 0° C., piperidine (128 ml) added and stirring continued at RT overnight. Sat'd aq. sodium bicarbonate is added to the mixture, the phases separated and the organic phase washed with sodium bicarbonate, sat'd NACl, dried, filtered and evaporated in vacuo. The residue is dissolved in toluene and evaporated in vacuo affording the desired product as the hydrochloride salt.

Quelle

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