HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234902Erstellt: 25. Oktober 2026
Ethyl Acetate → 2-butyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine
https://huagongshe.com/reaction/234902
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 2-Bromohexanoyl bromide | HCID 3016923 | — |
| Edukt | Benzoic acid, 4-amino-3-hydroxy-, methyl ester | HCID 7020619 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-butyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine | HCID 10539473 | 81,7% |
Reaktionsschritte
To a solution of 2-amino-5-methoxycarbonylphenol [Tetrahedron, 4.6 (15), 5177-5186 (1990)] (8.0 g) in a mixed solvent of ethyl acetate (200 ml) and water (200 ml) were added sodium hydrogen carbonate (11.18 g) and 2-bromohexanoyl bromide (12.73 g) and the mixture was stirred at room temperature for 10 minutes. The organic layer was separated and the solvent was distilled off under reduced pressure. The resulting residue was dissolved in dimethylformamide (300 ml), to the solution was added potassium carbonate (6.0 g) and the mixture was stirred at room temperature for 1 hour. Water was added to the reaction solution and extraction with ethyl acetate was conducted. The solvent was distilled off under reduced pressure and the resulting crystals were recrystallized from ether to give 2-butyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (10.3 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05597820 |
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| Quelldatensatz | uspto-grants-1997_01 |
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| ORD ID | ord-5e0192d32cc24e3e8c8abb93cd56ba12 |
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| Quellennotiz | uspto-grants-1997_01 |
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