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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010625Generated: October 26, 2026

Iodine → 4-Bromo-2-iodo-6-nitroaniline

https://huagongshe.com/reaction/1010625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-Bromo-2-nitroanilineHCID 70132—
CatalystSilver sulfateHCID 159865—
SolventEthanolHCID 702—
Product4-Bromo-2-iodo-6-nitroanilineHCID 1068870988%

Reaction Steps

4-Bromo-2-nitroaniline (14.3 g, 0.0659 mol) was added in one portion to iodine (17.6 g, 0.0692 mol) dissolved in ethanol (300 ml), followed by silver (I) sulphate (20.4 g 0.0659 mol). After stirring at ambient temperature for 18 hours the reaction was filtered and the solid obtained was washed with dichloromethane until all the orange product had dissolved. The combined filtrates were evaporated in vacuo and the resulting solid was washed with diethyl ether/40-60 Petroleum ether (1:1) and filtered to give 4-bromo-2-iodo-6-nitroaniline as an orange solid (19.8 g, 88%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977340B2
Source datasetuspto-grants-2011_07
ORD IDord-5bc3cf4b39e347a3a9399b5da706f73a
Source noteuspto-grants-2011_07