HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629242Generated: October 26, 2026
Acetic Acid → 3-Iodo-6-(phenylethynyl)pyridazine
https://huagongshe.com/reaction/629242
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 3-Chloro-6-(phenylethynyl)pyridazine | HCID 12680260 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | 3-Iodo-6-(phenylethynyl)pyridazine | HCID 57516773 | 58% |
Reaction Steps
To a solution of 100 mg (0.466 mmol) of 3-chloro-6-(phenylethynyl)pyridazine in 5 ml of acetonitrile were added sodium iodide (209 mg, 1.4 mmol, 3 equiv.), acetic acid (56 mg, 53.3 ml, 0.93 mmol, 2 equiv.), and 95% sulfuric acid (4.6 mg, 2.5 ml, 0.47 mmol, 1 equiv.). The orange solution was stirred for 8 hours at 70° C. and then left to cool overnight. After standard workup with ethyl acetate/water, the residue was adsorbed onto 4 g of silicagel and purified by flash chromatography over a 20 g silicagel column over a heptane to 50% ethyl acetate in heptane gradient to yield 82 mg (58% yield) of the title compound as a crystalline light yellow solid, MS: m/e=307.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315498B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-5a400e785db04073bb5d7ab8142e27c1 |
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| Source note | uspto-grants-2016_04 |
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