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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508369Generated: October 29, 2026

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

https://huagongshe.com/reaction/508369

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 numberUS09095590B2
Source datasetuspto-grants-2015_08
ORD IDord-ea3e4b8970114298868f402f1af3fb27
Source noteuspto-grants-2015_08