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Carbon Tetrachloride → Diethyl 3,4-dimethoxy-5-nitrobenzoylmalonate

HRID 274443
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 274443
[Mg].C(Cl)(Cl)(Cl)Cl.[C:7]([O:15][CH2:16][CH3:17])(=[O:14])[CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10].[CH3:18][O:19][C:20]1[CH:21]=[C:22]([CH:26]=[C:27]([N+:31]([O-:33])=[O:32])[C:28]=1[O:29][CH3:30])[C:23](Cl)=[O:24]>C(O)C.C1(C)C=CC=CC=1.O1CCCC1>[CH3:18][O:19][C:20]1[CH:21]=[C:22]([CH:26]=[C:27]([N+:31]([O-:33])=[O:32])[C:28]=1[O:29][CH3:30])[C:23]([CH:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[C:7]([O:15][CH2:16][CH3:17])=[O:14])=[O:24]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 5943Carbon TetrachlorideHCID 7761Diethyl MalonateHCID 5462224MagnesiumHCID 219286153,4-Dimethoxy-5-nitrobenzoyl chloride

Produkt 1

HCID 19000155Diethyl 3,4-dimethoxy-5-nitrobenzoylmalonate

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 702
Ethanol
Lösungsmittel
2×
HCID 1140TolueneLösungsmittel2×
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

4.9 g of magnesium are suspended in 15 ml of absolute ethanol and, after adding 1 ml of carbon tetra- chloride, warmed until the reaction starts. A solution of 31.8 g of diethyl malonate in 19.9 ml of absolute ethanol and 80 ml of absolute toluene is then added dropwise while stirring so that the temperature lies between 50° and 60°. The reaction mixture is subsequently stirred at this temperature for an additional 1 hour, whereupon it is cooled to -5° and a solution of 49.3 g of 3,4-dimethoxy-5-nitrobenzoyl chloride (m.p. 82°-85°) in 300 ml of absolute toluene and 50 ml of absolute tetrahydrofuran is added dropwise so that the temperature does not exceed -5°. The mixture is subsequently stirred at room temperature overnight. After distillation of the solvent the residue is dissolved in 500 ml of ethyl acetate. The solution is treated while stirring and cooling with ice with an ice-cold solution of 12 ml of concentrated sulfuric acid in 80 ml of water. The organic phase is washed with sodium chloride solution, dried over magnesium sulfate and evaporated. The oil obtained is chromatographed on a ten-fold amount of silica gel with methylene chloride. The crystalline material obtained is recrystallized from isopropyl ether. There is obtained diethyl 3,4-dimethoxy-5-nitrobenzoylmalonate in the form of pale beige crystals of m.p. 70°.

Aufarbeitung

  1. temperaturewarmed until the reaction
  2. customlies between 50° and 60°
  3. stirringThe reaction mixture is subsequently stirred at this temperature for an additional 1 hour, whereupon it
  4. temperatureis cooled to -5°
  5. customdoes not exceed -5°
  6. stirringThe mixture is subsequently stirred at room temperature overnight
  7. distillationAfter distillation of the solvent the residue
  8. dissolutionis dissolved in 500 ml of ethyl acetate
  9. additionThe solution is treated
  10. stirringwhile stirring
  11. temperaturecooling with ice with an ice-cold solution of 12 ml of concentrated sulfuric acid in 80 ml of water
  12. washThe organic phase is washed with sodium chloride solution
  13. dry with materialdried over magnesium sulfate
  14. customevaporated
  15. customThe oil obtained
  16. customis chromatographed on a ten-fold amount of silica gel with methylene chloride
  17. customThe crystalline material obtained
  18. customis recrystallized from isopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-1922e9b955fa4b8f83e14f29f03f4367
Quelldatensatz
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05389653

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