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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktSodium BicarbonateHCID 516892—
Edukt2-Bromohexanoyl bromideHCID 3016923—
EduktBenzoic acid, 4-amino-3-hydroxy-, methyl esterHCID 7020619—
LösungsmittelWaterHCID 962—
Produkt2-butyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazineHCID 1053947381,7%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05597820
Quelldatensatzuspto-grants-1997_01
ORD IDord-5e0192d32cc24e3e8c8abb93cd56ba12
Quellennotizuspto-grants-1997_01