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Dimethyl Sulfoxide → HCID 86646134, Verbindung

HRID 551643
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 551643
[Cl-].[Li+].CS(C)=O.[CH2:7]([C:10]([CH:21]([CH2:23][CH3:24])[CH3:22])(C(OCC)=O)[C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:8]=[CH2:9]>O>[CH:21]([CH:10]([CH2:7][CH:8]=[CH2:9])[C:11]([O:13][CH2:14][CH3:15])=[O:12])([CH2:23][CH3:24])[CH3:22]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 679Dimethyl SulfoxideHCID 433294Lithium ChlorideHCID 130107351,3-Diethyl 2-(1-methylpropyl)-2-(2-propen-1-yl)propanedioate

Produkt 1

HCID 86646134HCID 86646134, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel2×

Reaktionsbedingungen

Temperatur
185 °C

Versuchsvorschrift

Lithium chloride (9.67 g, 228.1 mmol) and water (2.05 mL, 113.9 mmol) were added to a dimethyl sulfoxide (60 mL) solution of diethyl allyl(sec-butyl)malonate (30.90 g, 120.5 mmol), and the mixture was stirred at 185° C. for 6 hours. The mixture was treated with water, followed by extraction with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure to obtain the compound of interest as a brown oil substance. This compound was used in the next reaction without being purified.

Aufarbeitung

  1. extractionfollowed by extraction with diethyl ether
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. distillationThen, the solvent was distilled off under reduced pressure
  4. customto obtain the compound of interest as a brown oil substance
  5. customThis compound was used in the next reaction
  6. customwithout being purified

Quellen und Nachweise

ORD-Eintrag
ord-44ebf61da33646538bc8984d8058ab46
Quelldatensatz
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07947738B2

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