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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348977Generated: October 25, 2026

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

https://huagongshe.com/reaction/348977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl bromideHCID 8002—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 8-iodo-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylateHCID 21086219—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductMethyl 4-butyl-8-iodo-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylateHCID 2108620472.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-453d63c5ea824b89aa84c6f2140e1f31
Source noteuspto-grants-2007_02