HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 4-Iodo-2-propylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Propylphenol | HCID 12570 | — |
| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Iodo-2-propylphenol | HCID 15171851 | — |
Reaction Steps
A mixture of 6.8 g (50 mmol) of 2-propylphenol. 8.25 g (55 mmol) of sodium iodide. 175 ml of acetonitrile and 40 ml of water was cooled on ice. t-Butylhypochlorite, 6 g or 6.56 ml (55 mmol), was added slowly at 0° . After stirring for 10 minutes at 0° , 500 ml of ethyl acetate was added and the mixture was washed with 5% aqueous solution of sodium thiosulfate. The organic layer was dried and evaporated and the residue was chromatographed over 150 g of silica gel using methylene chloride/hexane 3:2. The more polar monoiodinated product was crystallized from petroleum ether to give colorless crystals with m.p. 54°-56°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05015661 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-38b7fa4c82194d5091b383ca55d7867b |
| Source note | uspto-grants-1991_05 |