HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → Methyl 4-iodo-3-phenylisothiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Pentyl nitrite | HCID 10026 | — |
| Reactant | Methyl 4-amino-3-phenyl-1,2-thiazole-5-carboxylate | HCID 13073192 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 4-iodo-3-phenylisothiazole-5-carboxylate | HCID 58374164 | 58.2% |
Reaction Steps
To a solution of methyl 4-amino-3-phenylisothiazole-5-carboxylate (Preparation 103C, 700 mg, 2.99 mmol) in chloroform (80 mL) were added iodine (4019 mg, 15.84 mmol) and amyl nitrite (0.602 mL, 4.48 mmol). The resulting mixture was heated to reflux for 30 min. The reaction mixture was cooled to room temperature and washed with aqueous sodium thiosulfate and then water. The organic layer was dried over sodium sulfate. Removal of the solvent in vacuo and crystallization from ethanol yielded methyl 4-iodo-3-phenylisothiazole-5-carboxylate (600 mg, 1.738 mmol, 58.2% yield) as a pale yellow solid. The compound had an LC/MS M+1=346.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216972B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-6897a65a9f234ecab98806947d1450d7 |
| Source note | uspto-grants-2015_12 |