HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 1,3,5-Triiodo-2-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2,4,6-Triiodophenol | HCID 11862 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 1,3,5-Triiodo-2-methoxybenzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09095590B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-56d87b9055bb49e591b5f343a4ca9f79 |
| Source note | uspto-grants-2015_08 |