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Sodium Chloride → Ethyl 5-methyl-5-phenyl-4-pentenoate

HRID 840967
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 840967
CC(C)([O-])C.[K+].[Br-].[C:8]([CH2:13][CH2:14][CH2:15][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([O:10][CH2:11][CH3:12])=[O:9].[C:35]([C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1)(=O)[CH3:36].[Cl-].[Na+]>O.O1CCCC1>[CH3:36][C:35]([C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1)=[CH:15][CH2:14][CH2:13][C:8]([O:10][CH2:11][CH3:12])=[O:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 5234Sodium ChlorideHCID 7410AcetophenoneHCID 2773643(3-(Ethoxycarbonyl)propyl)triphenylphosphonium BromideHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 70170845Ethyl 5-methyl-5-phenyl-4-pentenoateAusbeute 95,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962
Water
Lösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A mixture of potassium tert-butoxide (10.27 g, 91.6 mmol), 3-carboethoxypropyltriphenylphosphonium bromide (41.87 g, 91.6 mmol) and tetrahydrofuran (300 ml) was stirred at room temperature. Acetophenone (10.0 g, 83.2 mmol) was added dropwise to the mixture, and the resulting mixture was stirred at room temperature for another 1 hour and then allowed to stand overnight. Water (100 ml) was added to the reaction mixture, and the resulting mixture was stirred at room temperature for 1 hour, poured into an aqueous sodium chloride solution, and then extracted twice with ethyl acetate. The extract solution was washed with a 5% aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: ethyl acetate/n-hexane=2/98) to obtain 17.3 g of ethyl 5-methyl-5-phenyl-4-pentenoate.

Aufarbeitung

  1. stirringthe resulting mixture was stirred at room temperature for another 1 hour
  2. stirringthe resulting mixture was stirred at room temperature for 1 hour
  3. extractionextracted twice with ethyl acetate
  4. washThe extract solution was washed with a 5% aqueous sodium chloride solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationThe solvent was distilled off under reduced pressure
  7. customthe resulting residue was purified by a silica gel column chromatography (eluent: ethyl acetate/n-hexane=2/98)

Quellen und Nachweise

ORD-Eintrag
ord-28ae1373664042af972861e6710defd4
Quelldatensatz
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06369110B1

Notizen zur Reaktion

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