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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486834Generated: October 30, 2026

Sulfuric Acid → 3,5-diiodonitrobenzene

https://huagongshe.com/reaction/486834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant2,6-Diiodo-4-nitroanilineHCID 79386—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product3,5-diiodonitrobenzeneHCID 12134256—

Reaction Conditions

Temperature0 °C

Reaction Steps

13.8 g (0.2M) of sodium nitrite was added portionwise slowly to 96 mL of conc. sulfuric acid at 0° C. The resulting thick mixture was stirred at 0° C. for 10 minutes. A suspension of 68.25 g (0.175M) of finely powdered 4-nitro-2,6-diiodoaniline in 175 mL of glacial acetic acid was added cautiously portionwise to the above mixture at 0° C. After the addition, the mixture was stirred 30 mins. The resulting slurry was then added slowly to a vigorously stirred suspension of 4 g of cuprous oxide in 420 mL of absolute ethanol over a period of 25 mins. Vigorous effervescence was observed during this addition. The resulting mixture was stirred 20 mins. at room temperature and then heated to reflux for 30 minutes. After cooling, this reaction mixture was poured onto a large amount of ice. The solid which separated was filtered, and washed with water. This solid was dissolved in a minimum amount of chloroform, dried over anhyd. magnesium sulfate, and the solvent was removed to give 62 g of 3,5-diiodnitrobenzene as a yellow solid. ##STR135##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292879
Source datasetuspto-grants-1994_03
ORD IDord-2711c1a386e540f9a45022d6f231138d
Source noteuspto-grants-1994_03