HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-iodothiazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazoline | HCID 54352089 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-iodothiazoline | HCID 53974764 | 14.3% |
Reaction Steps
A solution of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazoline (0.5 g) and N-iodosuccinimide (0.4 g) in chloroform (30 ml) was refluxed for 20 hours. After cooling, the reaction mixture was washed with an aqueous sodium sulfite solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was subjected to column chromatography to give 0.1 g of 2-ethoxycarbonylimino-3-(3-tri-fluoromethylphenyl)-5-iodothiazoline (Compound No. 42).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05426188 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-72ae534445ea4f8694ce3e8f636918ed |
| Source note | uspto-grants-1995_06 |