Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741581Generated: November 3, 2026

3,5-diiodonitrobenzene → 3,5-DIIODOANILINE

https://huagongshe.com/reaction/1741581

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-diiodonitrobenzeneHCID 12134256—
SolventEthanolHCID 702—
Product3,5-DIIODOANILINEHCID 12134254—

Reaction Steps

A mixture of 61.5 G (0.164M) of 3,5-diiodonitrobenzene, from step (a), and 111.1 G (0.4924M) of stannous chloride in 900 ml of absolute ethanol was heated to reflux 1.5 hours under nitrogen. Most of the solvent was removed. The residue was stirred with ethylacetate, 5 normal sodium hydroxide and ice. organic phase was separated and washed with saturated sodium chloride solution. After drying over anhydrous magnesium sulfate, solvent was removed to afford a crude oil, which was chromatographed on silica gel using 8:1:1 mixture of hexane:methylene chloride:ethyl acetate. The desired aniline was obtained as 35 G of light tan colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334590
Source datasetuspto-grants-1994_08
ORD IDord-c1e289040dd44b71a1985f72c9043e5c
Source noteuspto-grants-1994_08