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HRID 875186Erstellt: 24. Oktober 2026

Dimethylformamide → N-Methoxy-N,4-dimethyloxazole-5-carboxamide

https://huagongshe.com/de/reaction/875186

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Edukt4-Methyl-1,3-oxazole-5-carboxylic acidHCID 292311—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelThionyl ChlorideHCID 24386—
ProduktN-Methoxy-N,4-dimethyloxazole-5-carboxamideHCID 1892536948,1%

Reaktionsschritte

To a stirred solution of 4-methyl-1,3-oxazole-5-carboxylic acid (4.00 g, 31.5 mmol) in thionyl chloride (4 ml) were added 0.4 ml N,N-dimethylformamide and the mixture was refluxed for 2 hours. After cooling, the volatiles were removed in vacuo and the remaining material was suspended in tetrahydrofuran (10 ml). This suspension was added to a stirred suspension of N,O-dimethyl-hydroxylamine hydrochloride (3.38 g, 34.6 mmol) and triethylamine (9.55 g, 94.4 mmol) in tetrahydrofuran (10 ml). The reaction mixture was stirred at room temperature for 20 h. After evaporation of the solvent in vacuo dichloromethane and 1N HCl were added. The phases were separated, the organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. Purification of the crude material on silica gel afforded N-methoxy-N,4-dimethyl-1,3-oxazole-5-carboxamide (2.58 g, 45%) as an orange solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08981111B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-641a01cec1a04a67a708091d1e324a34
Quellennotizuspto-grants-2015_03