HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 339405Erstellt: 23. Oktober 2026
Methyl 2-methylfuran-3-carboxylate → 2-Methylfuran-3-carboxamide
https://huagongshe.com/de/reaction/339405
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl 2-methylfuran-3-carboxylate | HCID 80237 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | 1-(2-Methylfuran-3-yl)methanamine | HCID 18525866 | — |
| Lösungsmittel | Formamide | HCID 713 | — |
| Produkt | 2-Methylfuran-3-carboxamide | HCID 10772974 | 83% |
Reaktionsschritte
(2-Methylfuran-3-yl)methanamine: A solution of 10 mmol (1.256 ml) of methyl 2-methylfuran-3-carboxylate and 38.9 mmol (2.1 g) of NaOMe in 20 ml of formamide was stirred at 100° C. for 30 min. The reaction mixture was poured into ice-water (20 ml) and extracted with ethyl acetate (3×). The extract was dried over MgSO4 and concentrated to give 1.05 g (83%) of 2-methylfuran-3-carboxamide as oil (m/e=126.2 [M+1]). The amide was dissolved in dry THF (10 ml) and drop-wise added to 15 ml of 1M LiAlH4 with 15 ml THF at 0° C. under argon. Then the mixture was stirred for 5 hrs at 60° C. Following cooling, 50% aqueous THF (30 ml) was added to the mixture at 5-10° C. The resulting precipitate was removed by filtration and the filtered solution was dried and concentrated to give an oily product (0.93 g, 84%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08895050B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-26d6b62696d244cc975ac50e37f62d62 |
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| Quellennotiz | uspto-grants-2014_11 |
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