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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654492Generated: October 25, 2026

Sodium Iodide → 3-(4-Iodophenyl)pyridine

https://huagongshe.com/reaction/654492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(Pyridin-3-yl)anilineHCID 459522—
ReactantSodium AcetateHCID 517045—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product3-(4-Iodophenyl)pyridineHCID 12644356—

Reaction Steps

A mixture of 1.7 g (10 mmol) of 3-(4-aminophenyl)pyridine [F. S. Tanaka et al., J. Agric. Food Chem. 30, 957 (1982)], 17 ml of glacial acetic acid and 1.5 ml of trifluoroacetic acid was cooled in ice-water. Sodium nitrite, 0.8 g (11.4 mmol) was added in portions. After stirring for 15 minutes in ice-water and 15 minutes without cooling, 5 g of sodium iodide and 3 g of sodium acetate was added slowly with water cooling. The reaction mixture was diluted with 30 ml of water and stirred for 30 minutes. It was then partitioned between methylene chloride and 10% aqueous sodium carbonate solution. The organic phase was dried and evaporated and the residue was chromatographed over 20 g of silica gel using 10% (V/V) of ethyl acetate in methylene chloride. Crystallization from hexane yielded off-white crystals with m.p. 112°-115°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05132310
Source datasetuspto-grants-1992_07
ORD IDord-07823517a39d4ec7b69f3d3c56e3fa08
Source noteuspto-grants-1992_07