HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639486Generated: October 30, 2026
Water → 5-[4-(2-Hydroxyethyl)phenyl]dibenzothiophenium iodide
https://huagongshe.com/reaction/1639486
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Tetramethylammonium hydroxide | HCID 60966 | — |
| Reactant | HCID 87123706 | HCID 87123706 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-[4-(2-Hydroxyethyl)phenyl]dibenzothiophenium iodide | HCID 87123700 | 84% |
Reaction Steps
While cooling with ice, 10.0 g of dibenzothiophene-S-oxide synthesized in the above step (1) is added to 30 g of diphosphorus pentoxide/methanesulfonic acid (9/1), and further 10 ml of 2-phenylethyl acetate is added thereto. The reaction solution is stirred at room temperature for 6 hours, and then poured into ice water. The obtained aqueous solution is filtered, and 23 g of potassium iodide is added. Crystals precipitated are recovered by filtration to obtain 11.1 g of 5-[(4-(2-acetoxyethyl)-phenyl]dibenzothiophenium iodide. The obtained 11.1 g of 5-[4-(2-acetoxyethyl)-phenyl]dibenzothiophenium iodide is dissolved in 200 ml of methanol, 10.7 g of a 20% aqueous solution of tetramethylammonium hydroxide is added to the solution, followed by stirring at room temperature for 2 hours. Subsequently, 100 ml of ion exchange water and 100 ml of chloroform are added to the solution to extract a chloroform layer. After the solvent is distilled off under reduced pressure, the reaction product is washed with ethyl acetate to obtain 8.5 g of the aiming 5-[4-(2-hydroxyethyl)phenyl]dibenzothiophenium iodide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08110333B2 |
|---|
| Source dataset | uspto-grants-2012_02 |
|---|
| ORD ID | ord-9ea8312f4e3e4424872cd4ef209f6a30 |
|---|
| Source note | uspto-grants-2012_02 |
|---|