Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411194Generated: November 3, 2026

Sulfuric Acid → Methyl 4-bromo-2-iodobenzoate

https://huagongshe.com/reaction/2411194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfiteHCID 24437—
ReactantMethyl 2-Amino-4-bromobenzoateHCID 17871390—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductMethyl 4-bromo-2-iodobenzoateHCID 5848470782.7%

Reaction Conditions

Temperature5 °C

Reaction Steps

To methyl 2-amino-4-bromobenzoate (5.75 g) was added cooled 20% sulfuric acid (75 mL), sodium nitrite (2.07 g) was added by small portions under ice-cooling, and the mixture was stirred at the same temperature for 40 min. To this reaction mixture was added dropwise a solution of potassium iodide (8.3 g) in water (25 mL) under cooling to 5° C., 20% sulfuric acid (30 mL) was added, and the mixture was stirred at 5° C. for 2 hr. This reaction mixture was neutralized with 4N aqueous sodium hydroxide solution under ice-cooling, 10% aqueous sodium sulfite solution (45 mL) and sodium chloride were added, and the mixture was extracted with ethyl acetate. The organic layer was washed with 10% aqueous sodium sulfite solution added saturated brine and saturated brine, dried over sodium sulfate, and the solvent was evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate) to give the title compound (7.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-9dbbe8fcc9d74f33aa5bc7b25b6a800a
Source noteuspto-grants-2014_08