Reaktion #3869
ord-29d226711096432384d0866c11b1dd4d
Reaktionsgleichung
piperidine
product
7-Methoxy-3-hydroxy-2,2-dimethylbenzofuran
sodium bicarbonate
Methanesulfonyl chloride
→
desired product
7-Methoxy-3-piperidino-2,2-dimethylbenzofuran
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeat RT
- 2Temperaturcooled to 0° C.
- 3workup.STIRRINGstirring
- 4workup.WAITcontinued at RT overnight
- 5Sonstigethe phases separated
- 6Waschenthe organic phase washed with sodium bicarbonate
- 7Sonstigedried
- 8Filtrationfiltered
- 9Sonstigeevaporated in vacuo
- 10workup.DISSOLUTIONThe residue is dissolved in toluene
- 11Sonstigeevaporated 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.