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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375030Generated: October 25, 2026

2,3,5-Triiodobenzoic acid → 2,3,5-Triiodobenzoyl chloride

https://huagongshe.com/reaction/375030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,5-Triiodobenzoic acidHCID 6948—
ReactantOxalyl chlorideHCID 65578—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product2,3,5-Triiodobenzoyl chlorideHCID 2760806—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 15.0 g (30.0 mmol) of 2,3,5-triiodobenzoic acid and 19.0 g (150 mmol) of oxalyl chloride in 60 ml of dry dichloromethane was placed under nitrogen and cooled to 0° C. Two drops of dry DMF were added, the ice bath was removed and the resulting suspension was stirred at room temperature for 1.5 hrs. The resulting brown solution was concentrated in vacuo to produce a tan solid. The solid was dissolved in 30 ml of dry toluene and was concentrated in vacuo. The toluene concentration was repeated two more times to yield 2,3,5-triiodobenzoyl chloride as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484585
Source datasetuspto-grants-1996_01
ORD IDord-1597f145b8304576ab4ccfc670b2f5fc
Source noteuspto-grants-1996_01