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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886786Generated: November 4, 2026

Methanol → 1,3,5-Triiodo-2-methoxybenzene

https://huagongshe.com/reaction/1886786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2,4,6-TriiodophenolHCID 11862—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Solventtert-Butyl methyl etherHCID 15413—
Product1,3,5-Triiodo-2-methoxybenzeneHCID 18924259—

Reaction Steps

In a 250 mL pressure vessel was added 2,4,6-triiodophenol (5 g, 10.60 mmol) in MTBE (60 ml) to give a yellow solution. The solution was cooled in an ice bath and 2.0M trimethylsilyldiazomethane (7.95 ml, 15.90 mmol) was added at a fast drip followed by dropwise addition of methanol (6 mL) resulting in calm bubbling. The vessel was sealed and stirred at room temperature for 4 h. The reaction solution was partitioned between EtOAc and water and the organic layer was washed with 1M HCl, saturated NaHCO3, and saturated NaCl. The EtOAc was dried (MgSO4), filtered and concentrated to give a tan solid that was used without purification (4.8 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501238B2
Source datasetuspto-grants-2013_08
ORD IDord-0faa147f7a9640ba95403371ff0bb2ae
Source noteuspto-grants-2013_08