Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486835Generated: October 30, 2026

3,5-diiodonitrobenzene → 3,5-DIIODOANILINE

https://huagongshe.com/reaction/486835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-diiodonitrobenzeneHCID 12134256—
SolventEthanolHCID 702—
Product3,5-DIIODOANILINEHCID 1213425461.9%

Reaction Steps

A mixture of 61.5 g (0.164M) of 3,5-diiodonitrobenzene and 111.1 g (0.4924M) of stannous chloride in 900 mL of ethanol was heated to reflux 1.5 hrs under nitrogen. The reaction mixture was cooled and most of the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and excess ice-cold 5N sodium hydroxide and ice. The organic phase was separated, washed with sat'd sodium chloride solution, and dried over anhyd. magnesium sulfate. Solvent removal afforded a crude oil which was purified on silica gel using 8:1:1 mixture of hexane:methylene chloride:ethyl acetate to give 35 g of 3,5-diiodoaniline as a light tan colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292879
Source datasetuspto-grants-1994_03
ORD IDord-410acc0ad4a048879d6105580d543ac9
Source noteuspto-grants-1994_03