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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886166Generated: October 29, 2026

Triethylamine → N-(4-iodophenyl)-2-nitroaniline

https://huagongshe.com/reaction/1886166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-IodoanilineHCID 10893—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
SolventEthyl AcetateHCID 8857—
ProductN-(4-iodophenyl)-2-nitroanilineHCID 15045509—

Reaction Steps

According to the method of V. P. Chernetskii, A. I. Kiprianov, Zh. Obsch. Khim, 1956, 26, 3465, a mixture of 2-fluoronitrobenzene (14.0 g, 100 mmol), p-iodo aniline (10.95 g, 50 mmol) and triethylamine (13.9 ml, 100 mmol) was heated under reflux for 42 hours. The mixture was cooled, diluted with ethyl acetate (300 ml) washed consecutively with water (100 ml), 2N sodium hydroxide (100 ml) and brine (100 ml). The organic layer was dried (MgSO4), concentrated under reduced pressure and the residue was recrystallised from ethyl acetate to give N-(4-iodophenyl)-2-nitroaniline, 10.03 g, as bright orange needles, m.p. 171°-2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05149814
Source datasetuspto-grants-1992_09
ORD IDord-67ed1a8c194e4a9e80e251c7057524d6
Source noteuspto-grants-1992_09