HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Benzonitrile, 4-[(5-iodopentyl)oxy]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | 4-((5-Chloropentyl)oxy)benzonitrile | HCID 19381510 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzonitrile, 4-[(5-iodopentyl)oxy]- | HCID 16202445 | 99% |
Reaction Steps
While 50 g of 4-(5-chloro-pentoxy)-benzonitrile (8) prepared in Example 5 were added to 500 ml of 2-butanone and stirred, 167 g of sodium iodide were added. Subsequently, the reaction temperature was gradually increased and stirring was continued at 70-80° C. for 6 hr. After the reaction was completed, the reaction temperature was decreased to room temperature, and the resultant reaction mixture was added with 1 L of ethylacetate, and then washed with water and brine. The ethylacetate layer was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residual solution was crystallized with methylalcohol, thus obtaining 69.7 g (yield: 99%) of a title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585979B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-e4f7c9701fa94bc2b4963889c6315dde |
| Source note | uspto-grants-2009_09 |