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Water → Ethyl 5-methyl-1,3-oxazole-2-carboxylate

HRID 69089
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 69089
[CH2:1]([NH:5][C:6](=[O:12])[C:7]([O:9][CH2:10][CH3:11])=[O:8])[C:2]([CH3:4])=O.O=P(Cl)(Cl)Cl.O>C1(C)C=CC=CC=1>[CH3:4][C:2]1[O:12][C:6]([C:7]([O:9][CH2:10][CH3:11])=[O:8])=[N:5][CH:1]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 24813Phosphorus oxychlorideHCID 57348900Ethyl oxo[(2-oxopropyl)amino]acetate

Produkt 1

HCID 22099282Ethyl 5-methyl-1,3-oxazole-2-carboxylateAusbeute 61,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

To a stirred solution of ethyl 2-(acetonylamino)-2-oxo-acetate (9.2 g, 53.12 mmol) in toluene (100.0 mL), is added POCl3 (4.95 mL, 53.12 mmol) and the reaction mixture is refluxed for 16 hours. The reaction mixture is cooled, added portionwise to water (100.0 mL) and stirred vigorously. The organic layer is washed with saturated NaHCO3 solution (2×50 mL), water (2×50 mL), dried over Na2SO4, and evaporated under reduced pressure. The crude material is purified by silica gel chromatography eluting with hexane:ethyl acetate (8.0:2.0) to give the title compound (5.1 g, 61.9%) as a yellow oil. ESI/MS m/z 156.2.1 (M+H)+.

Aufarbeitung

  1. temperaturethe reaction mixture is refluxed for 16 hours
  2. temperatureThe reaction mixture is cooled
  3. washThe organic layer is washed with saturated NaHCO3 solution (2×50 mL), water (2×50 mL)
  4. dry with materialdried over Na2SO4
  5. customevaporated under reduced pressure
  6. customThe crude material is purified by silica gel chromatography
  7. washeluting with hexane:ethyl acetate (8.0:2.0)

Quellen und Nachweise

ORD-Eintrag
ord-eb3b587111da45c19727cb96ab7d371c
Quelldatensatz
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08822486B2

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