HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 6-Iodopyridine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | 6-Chloronicotinic acid | HCID 79222 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 6-Iodopyridine-3-carboxylic acid | HCID 819062 | — |
Reaction Steps
A mixture of 15.962 g ((0.106 mol) of sodium iodide in 51 g (30 ml, 40 mmol) of hydriodic acid were stirred for 5 minutes. To the mixture was added 17.184 g (0.109 mol) of 6-chloro-nicotinic acid and the resulting mixture refluxed at 100-130 C.°C. for 40 hours. The dark brown mixture was then taken up in 300 ml of acetone and stirred to dissolve the excess NaI. The product was collected by suction filtration, rinsed with 100 mL in 1N NaHSO3 and dried to give the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05468879 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-0aaa02c4385242519d249725f36a9c80 |
| Source note | uspto-grants-1995_11 |