HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 875186Erstellt: 24. Oktober 2026
Dimethylformamide → N-Methoxy-N,4-dimethyloxazole-5-carboxamide
https://huagongshe.com/de/reaction/875186
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Edukt | 4-Methyl-1,3-oxazole-5-carboxylic acid | HCID 292311 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Thionyl Chloride | HCID 24386 | — |
| Produkt | N-Methoxy-N,4-dimethyloxazole-5-carboxamide | HCID 18925369 | 48,1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08981111B2 |
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| Quelldatensatz | uspto-grants-2015_03 |
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| ORD ID | ord-641a01cec1a04a67a708091d1e324a34 |
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| Quellennotiz | uspto-grants-2015_03 |
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