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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62760Generated: October 30, 2026

Iodine → 2-Chloro-5-iodo-1,3-dimethoxybenzene

https://huagongshe.com/reaction/62760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantSodium IodideHCID 5238—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium NitriteHCID 23668193—
Reactant4-Chloro-3,5-dimethoxybenzenamineHCID 67041835—
SolventWaterHCID 962—
Product2-Chloro-5-iodo-1,3-dimethoxybenzeneHCID 6704173768.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Chloro-3,5-dimethoxyaniline (2) (6.61 g, 35.2 mmol) was added to a mixture of sulfuric acid (9.39 mL, 176 mmol) and H2O (100 mL) at 00° C. Sodium nitrite (3.16 g, 45.8 mmol) was added and the reaction mixture was stirred at 0° C. for 30 min. The mixture was added to a pre-warmed mixture of sodium iodide (21.1 g, 141 mmol), iodine (4.47 g, 17.6 mmol), sulphuric acid (8 mL) and H2O (100 mL) at 80° C. and the resulting mixture was heated at reflux for 30 min. The mixture was allowed to cool to RT and then 40% sodium thiosulfate solution (200 mL) was added. The product was extracted with EtOAc (300 mL), the solvent was removed in vacuo and the residue was purified by silica gel chromatography (120 g, 0-50% EtOAc in isohexanes) to afford 2-chloro-5-iodo-1,3-dimethoxybenzene (3) (7.16 g, 67% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447028B2
Source datasetuspto-grants-2016_09
ORD IDord-a7e27046576a44458eb50d74d470fc8c
Source noteuspto-grants-2016_09