HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 4-Iodomethyl-5-methyl-2-naphthalen-2-yloxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | 4-(Chloromethyl)-5-methyl-2-(naphthalen-2-yl)-1,3-oxazole | HCID 12158073 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Iodomethyl-5-methyl-2-naphthalen-2-yloxazole | HCID 21074268 | — |
Reaction Steps
1.8 g of 4-chloromethyl-5-methyl-2-naphthalen-2-yloxazole and 3 g of sodium iodide in 150 ml of acetone are heated under reflux for 2 hours. After the reaction mixture has been cooled, 300 ml of methyl tert-butyl ether are added, the mixture is washed three times with saturated Na2S2O3 solution and dried over MgSO4 and the solvents are then removed under reduced pressure. This gives 2.7 g of 4-iodomethyl-5-methyl-2-naphthalen-2-yloxazole as a light-yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07160911B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-fd05c981796b448b8502a53815ae871b |
| Source note | uspto-grants-2007_01 |