HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1886257Erstellt: 27. Oktober 2026
Triethylamine → N-hydroxy-N-(1-hydroxy-2-naphthyl)-4-methoxycarbonylbutanamide
https://huagongshe.com/reaction/1886257
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Monomethyl glutarate | HCID 73917 | — |
| Edukt | Potassium bisulfate | HCID 516920 | — |
| Edukt | 1-Hydroxy-2-naphthylhydroxylamine hydrochloride | HCID 85613850 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-hydroxy-N-(1-hydroxy-2-naphthyl)-4-methoxycarbonylbutanamide | HCID 9882881 | 56% |
Reaktionsschritte
Into a solution of 2 g (9.5 mmol) of 1-hydroxy-2-naphthylhydroxylamine hydrochloride in THF (10 ml) and water (2 ml) was added 2 ml (14.2 mmol) of triethylamine, the mixture was cooled to 0° C., and 395 mg (2.4 mmol) of acid chloride of 4-methoxycarbonylbutanoic acid was added followed by stirring at room temperature. Aqueous KHSO4 was then added and the mixture extracted with CH2Cl2. The organic layer was dried over anhydrous magnesium sulfate, the solvent was removed under a reduced pressure, and the residue subjected to silica gel column chromatography to give 405 mg (56%) of a hydroxyamic acid derivative.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05149859 |
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| Quelldatensatz | uspto-grants-1992_09 |
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| ORD ID | ord-86ac543fa22749e18aab843bc2f5ad89 |
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| Quellennotiz | uspto-grants-1992_09 |
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