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1,1-Dimethoxyethyl(dimethyl)amine → 3-(3-Methyl-1,2,4-oxadiazol-5-yl)benzaldehyde

HRID 1267121
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1267121
O1CC[O:3][CH:2]1[C:6]1[CH:7]=[C:8]([CH:12]=[CH:13][CH:14]=1)[C:9]([NH2:11])=[O:10].CO[C:17](OC)([N:19](C)C)[CH3:18]>>[CH3:18][C:17]1[N:11]=[C:9]([C:8]2[CH:7]=[C:6]([CH:14]=[CH:13][CH:12]=2)[CH:2]=[O:3])[O:10][N:19]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 878351,1-Dimethoxyethyl(dimethyl)amineHCID 18545471HCID 18545471, Verbindung

Produkt 1

HCID 185455103-(3-Methyl-1,2,4-oxadiazol-5-yl)benzaldehydeAusbeute 102,7 %

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

A mixture of 3-[1,3]dioxolan-2-yl-benzamide (2.3 g) and dimethylacetamide dimethylacetal (4 g) was heated under reflux for 1 hour and then evaporated to dryness. The oily residue was dissolved in dioxane (20 mL) and hydroxylamine hydrochloride (1.18 g), acetic acid (20 mL) and a 2N aqueous sodium hydroxide solution (9 mL) were added and the mixture was heated at 90° C. for 2 hours. After evaporation, the residue was dissolved in toluene (100 mL) and a 1N hydrochloric acid solution (50 mL) was added and the mixture was stirred at reflux for 2 hours. After cooling at room temperature the organic phase was decanted, washed with water, dried over Na2SO4, filtered and evaporated to give the title compound (2.3 g) as a white solid.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureunder reflux for 1 hour
  3. customevaporated to dryness
  4. dissolutionThe oily residue was dissolved in dioxane (20 mL)
  5. additionhydroxylamine hydrochloride (1.18 g), acetic acid (20 mL) and a 2N aqueous sodium hydroxide solution (9 mL) were added
  6. customAfter evaporation
  7. dissolutionthe residue was dissolved in toluene (100 mL)
  8. additiona 1N hydrochloric acid solution (50 mL) was added
  9. temperatureat reflux for 2 hours
  10. temperatureAfter cooling at room temperature the organic phase
  11. customwas decanted
  12. washwashed with water
  13. dry with materialdried over Na2SO4
  14. filtrationfiltered
  15. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-627812b91be54b5c8e9f2a7ad0539939
Quelldatensatz
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06552022B1

Notizen zur Reaktion

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