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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249862Generated: October 26, 2026

2,4-Dimethoxy-1-nitrobenzene → 1,5-Dimethoxy-2-iodo-4-nitrobenzene

https://huagongshe.com/reaction/1249862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dimethoxy-1-nitrobenzeneHCID 78633—
ReactantTrimethylbenzylammonium DichloroiodateHCID 56924451—
CatalystZincchlorideHCID 3007855—
SolventAcetic AcidHCID 176—
Product1,5-Dimethoxy-2-iodo-4-nitrobenzeneHCID 18542969—

Reaction Steps

To a solution of 2,4-dimethoxy-nitrobenzene (1.0 g) in glacial acetic acid (30 mL) is added benzyltrimethylammonium dichloroiodate (1.90 g) and anhydrous zinc chloride (1.0 g) and the mixture is stirred at room temperature under an atmosphere of argon. Additional benzyltrimethylammonium dichloroiodate (0.4 g) is added after 5 hours and again after 24 hours. Additional zinc chloride (0.5 g) and glacial acetic acid (15 mL) is added after 24 hours. The mixture is permitted to stir at room temperature for 3 days and is then filtered, diluted with 5% aqueous sodium bisulfite, and extracted three times with ethyl acetate. These pooled organic extracts are washed successively with 5% aqueous sodium bisulfite, saturated aqueous sodium chloride, then dried over anhydrous magnesium sulfate. After removal of the solvent under reduced pressure the residue is triturated with hexanes to provide the desired product as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335350B1
Source datasetuspto-grants-2002_01
ORD IDord-962857b8d41a4155be88fc6426bd020a
Source noteuspto-grants-2002_01