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Ethanol → HCID 13039291, Verbindung

HRID 1106345
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1106345
[Br:1][C:2]1[CH:25]=[CH:24][C:5]([O:6][C@H:7]2[CH2:12][CH2:11][N:10](C(OCC)=O)[CH2:9][C@H:8]2[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:4][CH:3]=1.[OH-].[Na+].C(O)C>CCCCCC>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][C@H:7]2[CH2:12][CH2:11][NH:10][CH2:9][C@H:8]2[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:24][CH:25]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 70531710HCID 70531710, Verbindung

Produkt 1

HCID 13039291HCID 13039291, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8058HexaneLösungsmittel

Versuchsvorschrift

A mixture of 7.28 g of cis-4-(4-bromophenoxy)-1-ethoxycarbonyl-3-phenylpiperidine, 48 ml of 20% aqueous sodium hydroxide solution and 90 ml of absolute ethanol is refluxed overnight under nitrogen. The mixture is cooled and partitioned between 50 ml of water and 100 ml of ether. The aqueous phase is extracted with ether (100 ml), and the combined organic phases are concentrated in vacuo. The resulting solid is dissolved in dichloromethane (100 ml) and washed with saturated sodium chloride solution. After drying over anhydrous sodium sulfate, filtration and concentration in vacuo affords a nearly colorless solid. The solid is dissolved in 200 ml of boiling hexane and the solution is reduced after boiling down in volume to about 150 ml. The solution is filtered, allowed to cool to room temperature and refrigerated overnight to afford product as a nearly colorless, crystalline solid, mp 113°-115° C.

Aufarbeitung

  1. temperatureis refluxed overnight under nitrogen
  2. temperatureThe mixture is cooled
  3. custompartitioned between 50 ml of water and 100 ml of ether
  4. extractionThe aqueous phase is extracted with ether (100 ml)
  5. concentrationthe combined organic phases are concentrated in vacuo
  6. dissolutionThe resulting solid is dissolved in dichloromethane (100 ml)
  7. washwashed with saturated sodium chloride solution
  8. dry with materialAfter drying over anhydrous sodium sulfate, filtration and concentration in vacuo
  9. customaffords a nearly colorless solid
  10. filtrationThe solution is filtered
  11. customto afford product as a nearly colorless, crystalline solid, mp 113°-115° C.

Quellen und Nachweise

ORD-Eintrag
ord-d4cdfd1c7cb04b1ca4f0ad6b3c7c454b
Quelldatensatz
uspto-grants-1982_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04312876

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