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Phosphorus oxide (P4O10) → Methyl 5-methoxy-1,3-oxazole-2-carboxylate

HRID 1817293
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1817293
O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.[CH3:15][O:16][C:17](=[O:26])[C:18]([NH:20][CH2:21][C:22]([O:24][CH3:25])=O)=[O:19]>C(#N)C>[CH3:25][O:24][C:22]1[O:19][C:18]([C:17]([O:16][CH3:15])=[O:26])=[N:20][CH:21]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14812Phosphorus oxide (P4O10)HCID 560326Dimethyloxalylglycine

Produkt 1

HCID 1491126Methyl 5-methoxy-1,3-oxazole-2-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

To a warm (35-40° C.) suspension of phosphorous pentoxide (77.7 g, 109 mmol) in anhydrous acetonitrile (200 mL) was added methyl[(2-methoxy-2-oxoethyl)amino](oxo)acetate (19.19 g, 109.6 mmol). The reaction mixture was heated to 65° C., then stirred overnight at room temperature. The product mixture was cooled to 0° C. and carefully quenched with ice and brine keeping the reaction from generating an unsuitable exotherm. The resultant mixture was extracted with ethyl acetate (600 mL). The organic extract was washed with brine, dried with Na2SO4, then concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with 100% CH2Cl2. The appropriate fractions were combined and concentrated to afford the title compound as a light yellow solid that was used without further purification.

Aufarbeitung

  1. temperatureTo a warm
  2. temperatureThe product mixture was cooled to 0° C.
  3. customcarefully quenched with ice and brine keeping
  4. customthe reaction
  5. extractionThe resultant mixture was extracted with ethyl acetate (600 mL)
  6. extractionThe organic extract
  7. washwas washed with brine
  8. dry with materialdried with Na2SO4
  9. concentrationconcentrated under vacuum
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-73364039a1844d138608c16198ebf673
Quelldatensatz
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07598264B2

Notizen zur Reaktion

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