HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 3-Chloro-2-iodo-5-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,3-Dichloro-5-nitropyridine | HCID 2763106 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Chloro-2-iodo-5-nitropyridine | HCID 36995452 | 91.2% |
Reaction Steps
A solution of 2,3-dichloro-5-nitropyridine (9.75 g) and potassium iodide (29 g) in acetic acid (120 mL, degassed with nitrogen) was heated to 100° C. for 1.5 hours under nitrogen. The brown solution was cooled to room temperature and then ethyl acetate (300 mL) added. The organic phase was separated and washed with water (2×100 mL) and dilute aqueous sodium sulfite (100 mL). Evaporation of the solvent gave crystalline 3-chloro-2-iodo-5-nitro-pyridine (13.11 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09162986B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-b51c3e2b58094760992327af6839ee82 |
| Source note | uspto-grants-2015_10 |