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Water → Diethyl-2-ethyl-2-(3-cyclohexylpropyl)-malonate

HRID 27305
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 27305
[Na].[CH2:2]([CH:4]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH3:3].[Na][C:16](C(CC)(CC)C)(C([O-])=O)[C:17]([O-])=O.O.[C:30]1([CH3:37])[C:31](C)=[CH:32][CH:33]=[CH:34][CH:35]=1>C1(C)C=CC=CC=1>[CH2:8]([O:7][C:5](=[O:6])[C:4]([CH2:16][CH3:17])([CH2:2][CH2:3][CH2:37][CH:30]1[CH2:35][CH2:34][CH2:33][CH2:32][CH2:31]1)[C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH3:9]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 962WaterHCID 7237O-XyleneHCID 8610Diethyl ethylmalonateHCID 5360545SodiumHCID 178443961HCID 178443961, Verbindung

Produkt 1

HCID 23344469Diethyl-2-ethyl-2-(3-cyclohexylpropyl)-malonate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

Sodium metal (3.16 g, 0.137 g/atom) was dispersed by heating with rapid stirring in 80 ml of dry xylene at 110° to 120° C. The mixture was cooled and the xylene was removed with a filter stick. Dry toluene (300 ml distilled from calcium hydride) was added thereto and followed by the addition of 28.17 g (0.149 mole) of diethyl ethylmalonate. This mixture was slowly heated to 150° C. 3-Cyclohexylpropyl-1-tosylate (28.3 g, 1.1956 mole; prepared by Example 10A) was dissolved in 80 ml of dry toluene. This solution was then added to the sodiodiethylethylmalonate above and the mixture was stirred at 150° C. for 10 hr. The mixture was cooled and poured into 500 ml of water. The phases were separated and the aqueous phase was extracted with 500 ml (2×250 ml) of ether. The ether extract was washed with 250 ml of saturated sodium chloride solution, dried over a anhydrous magnesium sulfate and filtered. The solvents were removed in vacuo. The product was distilled at reduced pressure to yield 19.4 g of the title compound having the following physical characteristics:

Aufarbeitung

  1. temperatureby heating
  2. temperatureThe mixture was cooled
  3. customthe xylene was removed with a filter stick
  4. additionDry toluene (300 ml distilled from calcium hydride) was added
  5. temperatureThe mixture was cooled
  6. customThe phases were separated
  7. extractionthe aqueous phase was extracted with 500 ml (2×250 ml) of ether
  8. extractionThe ether extract
  9. washwas washed with 250 ml of saturated sodium chloride solution
  10. dry with materialdried over a anhydrous magnesium sulfate
  11. filtrationfiltered
  12. customThe solvents were removed in vacuo
  13. distillationThe product was distilled at reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-15489f8eb5c34cd1b606a254e022aeb4
Quelldatensatz
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04220795

Notizen zur Reaktion

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