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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922833Generated: October 25, 2026

Sulfuric Acid → 1-Chloro-2-iodo-4-nitrobenzene

https://huagongshe.com/reaction/922833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
Reactant2-Chloro-5-nitroanilineHCID 22691—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product1-Chloro-2-iodo-4-nitrobenzeneHCID 31271473.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

An alternative synthetic procedure is as follows. 75 g (435 mmol) of 2-chloro-5-nitroaniline was added to a solution of water (600 mL) and conc. sulfuric acid (60 mL) in a 3 L 3-neck flask equipped for mechanical stirring. The solution was cooled to 0° C. and a solution of sodium nitrite (34.2 g, 496 mmol) in water (130 mL) was added slowly. The mixture was stirred for ½ hr. and then a solution of potassium iodide (130 g, 783 mmol) in water (520 mL) was added dropwise over ½ hr keeping the temperature below 15° C. The solution was stirred for 2 hr, then extracted with EtOAc (3×500 mL). The combined organic extracts were washed with sat. Na2S2O3 (2×500 mL), dried (Na2SO4), and concentrated. The crude iodide was dissolved in hot iPrOH (500 mL) and hexanes (200 mL) were added. The reaction was allowed to cool with stirring and the product was collected by suction filtration after stirring at 0° C. for 2 hr yielding 90 g (318 mmol, 73%) 2-chloro-5-nitro-iodobenzene as a light tan crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278961B2
Source datasetuspto-grants-2016_03
ORD IDord-409acd76f50b41989ab5b3943461827c
Source noteuspto-grants-2016_03