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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033753Generated: October 26, 2026

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

https://huagongshe.com/reaction/1033753

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 numberUS05312616
Source datasetuspto-grants-1994_05
ORD IDord-3463979439bd49ae9050ada73b8dc1ce
Source noteuspto-grants-1994_05