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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050960Generated: October 25, 2026

Sodium Iodide → 3-(4-Iodophenyl)pyridine

https://huagongshe.com/reaction/2050960

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 numberUS05015661
Source datasetuspto-grants-1991_05
ORD IDord-4e128241d5d64e5384a45117a0daf3f9
Source noteuspto-grants-1991_05