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Water → Ethyl 4-[1-benzyl-1,2,3,6-tetrahydropyrid-4-yl]benzoate

HRID 1059323
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1059323
Br[C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH2:9][CH2:10][N:11]([CH2:14][C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[CH2:12][CH:13]=2)=[CH:4][CH:3]=1.C([Li])CCC.[C:26](=O)([O:30]CC)[O:27][CH2:28][CH3:29].O>O1CCCC1.CCCCCC>[CH2:14]([N:11]1[CH2:12][CH:13]=[C:8]([C:5]2[CH:6]=[CH:7][C:2]([C:26]([O:27][CH2:28][CH3:29])=[O:30])=[CH:3][CH:4]=2)[CH2:9][CH2:10]1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 962WaterHCID 7766Diethyl CarbonateHCID 112443314-(4-Bromophenyl)-1,2,3,6-tetrahydro-1-(phenylmethyl)pyridineHCID 178418339Butyllithium

Produkt 1

HCID 11450082Ethyl 4-[1-benzyl-1,2,3,6-tetrahydropyrid-4-yl]benzoate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028
Tetrahydrofuran
Lösungsmittel
HCID 8058HexaneLösungsmittel

Versuchsvorschrift

To a solution of 11 g of 4-(4-bromophenyl)-1-benzyl-1,2,3,6-tetrahydropyridine in 200 ml of tetrahydrofuran was added 27 ml of a 2.5 M solution of n-butyllithium in hexane at −78° C. and the resulting mixture was stirred at the same temperature for 15 minutes. Into the reaction mixture was dropped 42 ml of diethyl carbonate and the mixture was heated to room temperature over 15 minutes. After adding water, the reaction mixture was extracted with ethyl acetate, washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (eluted with n-hexane/ethyl acetate) to thereby give 2.8 g of the title compound as a yellow oily substance.

Aufarbeitung

  1. extractionthe reaction mixture was extracted with ethyl acetate
  2. washwashed with a saturated aqueous solution of sodium chloride
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationAfter distilling off the solvent under reduced pressure
  5. customthe residue was purified by silica gel column chromatography (eluted with n-hexane/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-a35b3606e33445a8b769d15d115beedf
Quelldatensatz
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06518423B1

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