HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 1-(4-Hydroxy-3,5-di-isopropylphenyl)-2-iodo-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-Chloro-1-(4-hydroxy-3,5-di-isopropylphenyl)-ethanone | HCID 85890059 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 1-(4-Hydroxy-3,5-di-isopropylphenyl)-2-iodo-ethanone | HCID 57747236 | 70% |
Reaction Steps
To a solution of 50.95 g (200 mmol) of 2-chloro-1-(4-hydroxy-3,5-di-isopropylphenyl)-ethanone in 250 ml of 1,2-dimethoxyethane, a solution of 30.94 g (206 mmol) of sodium iodide in 250 ml of 1,2-dimethoxyethane is added dropwise at room temperature. After the addition, stirring is continued for 16 hours at room temperature. Then 100 ml of hexane is added and, after stirring for additional 15 minutes, the precipitated salts are removed by filtration. The obtained solution is evaporated and the resulting residue is purified by recrystallization from hexane/dichloromethane to give 48.5 g (70%) of compound 201, m.p. 127-128° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820865B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-dfe52df670cf4c17b912d63c42a70261 |
| Source note | uspto-grants-2010_10 |