HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4,6-Triiodophenol → 2,4,6-Triiodophenyl (2-propyl)pentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4,6-Triiodophenol | HCID 11862 | — |
| Reactant | 2-Propylvaleryl chloride | HCID 76240 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,4,6-Triiodophenyl (2-propyl)pentanoate | HCID 86747892 | 68% |
Reaction Steps
A mixture of 2,4,6-triiodophenol (2.0 g, 4.24 mmol), 2-propylvaleroyl chloride (2.5 ml, 12.7 mmol, 3 eq) and 4-dimethylaminopyridine (DMAP; 20 mg) in 20 ml of acetonitrile was refluxed under argon overnite. The reaction mixture was cooled and poured into excess aqueous sodium bicarbonate and then extracted with dichloromethane. The dichloromethane extract was dried over magnesium sulfate, filtered, and evaporated to give the crude product (2.42 mmol, 95%) as a pink solid. Recrystallization from ethyl acetate gave 1.75 g (68%) of pure product, mp 99°-101° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05468466 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-8b105aff4e6d46b4b92270d2ff404464 |
| Source note | uspto-grants-1995_11 |