Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 67472041 | HCID 67472041 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67169575 | HCID 67169575 | 21.4% |
Reaction Steps
To methyl 5-phenylisothiazole-3-carboxylate (500 mg, 2.280 mmol) in a tube were added iodine (579 mg, 2.280 mmol) and nitric acid (2.280 mmol). The resulting mixture was heated to 80° C. for 1 h. After the reaction was cooled to room temperature, EtOAc (50 mL) was added. The resulting mixture was washed with saturated Na2S2O3 solution until the brown color disappeared. The organic layer was concentrated. HPLC and flash chromatography yielded methyl 4-iodo-5-phenylisothiazole-3-carboxylate (168 mg, 0.487 mmol, 21.34% yield). The compound had an LC/MS M+1=345.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09216972B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-7158e76fefc94397ab92cddacfb0a844 |
|---|
| Source note | uspto-grants-2015_12 |
|---|