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Dimethylformamide → 2-(3-Cyano-4-nitrophenyl)-2-methyl-1,3-dioxolane

HRID 1087190
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1087190
Cl[C:2]1[CH:3]=[C:4]([C:11]2([CH3:16])[O:15][CH2:14][CH2:13][O:12]2)[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9].C(=O)(O)[O-].[Na+].C(OCC)(=O)C.[CH3:28][N:29](C)C=O>>[C:28]([C:2]1[CH:3]=[C:4]([C:11]2([CH3:16])[O:15][CH2:14][CH2:13][O:12]2)[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9])#[N:29]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 516892Sodium BicarbonateHCID 100374432-(3-Chloro-4-nitrophenyl)-2-methyl-1,3-dioxolane

Produkt 1

HCID 100142372-(3-Cyano-4-nitrophenyl)-2-methyl-1,3-dioxolane

Versuchsvorschrift

A mixture of 2-(3-chloro-4-nitrophenyl)-2-methyl-1,3-dioxolane (9.8 g) and cuprous cyanide (4.0 g) in N,N-dimethylformamide (20 ml) was stirred and refluxed for 11 hours. An aqueous solution of sodium bicarbonate (200 ml) and ethyl acetate (100 ml) were added to the reaction mixture. The mixture was stirred and filtered. The filtrate was separated and the organic layer was dried and evaporated. The oily residue was purified by column chromatography on silica gel (200 g) eluting with a mixture of toluene and ethyl acetate (20:1) to give yellow plates of 2-(3-cyano-4-nitrophenyl)-2-methyl-1,3-dioxolane (4.6 g).

Aufarbeitung

  1. temperaturerefluxed for 11 hours
  2. stirringThe mixture was stirred
  3. filtrationfiltered
  4. customThe filtrate was separated
  5. customthe organic layer was dried
  6. customevaporated
  7. customThe oily residue was purified by column chromatography on silica gel (200 g)
  8. washeluting with a mixture of toluene and ethyl acetate (20:1)

Quellen und Nachweise

ORD-Eintrag
ord-0f93b2f3423b45ebbe194eaa33773e46
Quelldatensatz
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05034417

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