Reaktion #3863

ord-649ea945dd7e4b54ae14924d504966d6

Reaktionsgleichung

C1CCNCC1
Piperidine
CS(=O)(=O)Cl
Methane sulfonyl chloride
COc1ccc2c(c1)C(O)CCO2
product
COc1ccc2c(c1)C(O)CCO2
6-Methoxy-4-hydroxy-2,3-dihydrobenzopyran
O=C([O-])O.[Na+]
sodium bicarbonate
COc1ccc2c(c1)C(N1CCCCC1)CCO2
desired product
COc1ccc2c(c1)C(N1CCCCC1)CCO2
6-Methoxy-4-piperidino-2,3-dihydrobenzopyran

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled to 0° C
  2. 2
    workup.STIRRINGthe solution stirred at RT overnight
  3. 3
    workup.STIRRINGthe mixture is stirred for 30 minutes
  4. 4
    SonstigeThe organic layer is separated
  5. 5
    Waschenwashed with sat'd NaCl
  6. 6
    Sonstigedried
  7. 7
    FiltrationThe solution is filtered
  8. 8
    Sonstigethe filtrate evaporated in vacuo

Vorschrift

Methane sulfonyl chloride (14.9 ml) is added dropwise to a stirred solution of the product obtained in Step 1. (31.6 g) and triethylamine (29.3 ml) in methylene chloride (750 ml) cooled to 0° C. under nitrogen. The reaction mixture is stirred at RT for 21/2 hours and cooled to 0° C. Piperidine (175 ml) is added to the cooled reaction mixture and the solution stirred at RT overnight. Sat'd aq. sodium bicarbonate is added to the solution and the mixture is stirred for 30 minutes. The organic layer is separated, washed with sat'd NaCl and dried. The solution is filtered and the filtrate evaporated in vacuo yielding the desired product as its hydrochloride salt.

Quelle

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