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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871962Generated: October 31, 2026

Potassium Iodide → Methyl 6-bromo-3-[(2-ethoxycarbonyl)propan-2-yl]amino-2-nitrobenzoate

https://huagongshe.com/reaction/871962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
ReactantMethyl 3-amino-6-bromo-2-nitrobenzoateHCID 58891824—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductMethyl 6-bromo-3-[(2-ethoxycarbonyl)propan-2-yl]amino-2-nitrobenzoateHCID 6721081331%

Reaction Steps

The mixture of methyl 3-amino-6-bromo-2-nitrobenzoate (Reference Compound No. 1-(4), 11.6 g, 42.0 mmol), ethyl 2-bromoisobutyrate (60.4 mL, 412 mmol), potassium iodide (7.76 g, 46.2 mmol) and cesium carbonate (56.1 g, 172 mmol) was stirred at 85° C. for 4 days. After the mixture was cooled down, ethyl acetate (500 mL) and water (500 mL) were added thereto, the mixture was partitioned, and then the water layer was extracted with ethyl acetate (300 mL). The organic layer was combined, washed with water (1 L, 2 times) and saturated brine (1 L) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (5.08 g) as an orange oil. (Yield 31%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975256B2
Source datasetuspto-grants-2015_03
ORD IDord-5fa380c36c3841538b1a1e43f565ed85
Source noteuspto-grants-2015_03