Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 348977Erstellt: 23. Oktober 2026

Butyl bromide → Methyl 4-butyl-8-iodo-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate

https://huagongshe.com/de/reaction/348977

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButyl bromideHCID 8002—
EduktPotassium CarbonateHCID 11430—
EduktMethyl 8-iodo-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylateHCID 21086219—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
ProduktMethyl 4-butyl-8-iodo-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylateHCID 2108620472,6%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of Methyl 8-iodo-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate (2.64 g) and potassium carbonate (5 g) in DMSO (20 mL) was added bromobutane (5 g), and the reaction mixture was stirred for 1 h at 80° C. The mixture was cooled to room temperature, diluted with 1:1 ethyl acetate/hexanes (100 mL) and water (160 mL), and separated. The organic layer was washed with water, and brine, dried (magnesium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:10 ethyl acetate/hexanes) afforded 2.24 g of the title compound: 1H NMR (300 MHz, CDCl3) δ 8.13, 7.63, 4.74, 3.96, 3.92, 1.64, 1.42, 0.97.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176242B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-453d63c5ea824b89aa84c6f2140e1f31
Quellennotizuspto-grants-2007_02