Reaktion #219951

Reaktionsgleichung

ethyl 2-oxocyclopentane carboxylate

potassium carbonate

1-bromo-n-hexane

→

Ethyl 1-n-hexyl-2-oxocyclopentane carboxylate

Ausbeute 87.3%

Lösungsmittel

acetone

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGThe reaction mixture was further stirred for about 15 minutes
2. 2
   workup.ADDITIONUpon the completion of the addition
3. 3
   Temperaturthe reaction mixture was heated
4. 4
   Temperaturfor reflux for 5 hours
5. 5
   FiltrationThe reaction mixture was filtered under the reduced pressure
6. 6
   Waschenthe filter cake was washed with diethyl ether until its color
7. 7
   SonstigePale yellow filtrate was collected
8. 8
   Trocknendried over anhydrous magnesium sulfate
9. 9
   Sonstigethe solvent was removed
10. 10
    workup.DISTILLATIONThe residue was distilled under reduced pressure, and 41.89 g of colorless liquid as a distillate cut of 156-160° C./23 mmHg
11. 11
    Sonstigewas collected

Vorschrift

Under vigorously agitation, 31.2 g of ethyl 2-oxocyclopentane carboxylate was added to 84.5 g purity of 98%) of ground anhydrous potassium carbonate, and after stirring for several minutes, to the mixture was added 100 ml Of acetone. The reaction mixture was further stirred for about 15 minutes, then thereto was dropwise added 57.54 ml (purity of 98%) of 1-bromo-n-hexane. Upon the completion of the addition, the reaction mixture was heated for reflux for 5 hours. The reaction mixture was filtered under the reduced pressure, and the filter cake was washed with diethyl ether until its color was purely white. Pale yellow filtrate was collected and dried over anhydrous magnesium sulfate, then the solvent was removed. The residue was distilled under reduced pressure, and 41.89 g of colorless liquid as a distillate cut of 156-160° C./23 mmHg was collected. Yield: 87.3%. MS: m/e 240(M+′), 212(M+′—CH2CH2), 195(M+′—OCH2CH3), 167(M+′—CO2CH2CH3), 156(base), 155, 127, 111.

Quelle