HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → HCID 178517798, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | HCID 178524771 | HCID 178524771 | — |
| Product | HCID 178517798 | HCID 178517798 | — |
Reaction Steps
Alternatively, the present compound is prepared by reacting 5-chloro-6-hydroxynicotinic acid with I2 in an aqueous alkaline iodide solution to form 3-chloro-5-iodo-2-pyridinol. This reaction is conveniently conducted at an elevated temperature of between 40° C. and 150° C. and preferably at about 100° C. Lowering the pH of the reaction mixture to ≤1 such as, for example, by addition to the reaction mixture of SO2, will precipitate the 3-chloro-5-iodo-2-pyridinol from the reaction mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04517368 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-de22360abd0e4778a4d43bb0df3d9b6c |
| Source note | uspto-grants-1985_05 |