HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84324Generated: October 25, 2026
Potassium Iodide → 1-Dodec-7-ynyl-3,5-dimethyl-pyridinium iodide
https://huagongshe.com/reaction/84324
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3,5-Dimethylpyridine | HCID 11565 | — |
| Reactant | 12-Chloro-5-dodecyne | HCID 123509 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-Dodec-7-ynyl-3,5-dimethyl-pyridinium iodide | HCID 24781252 | 78% |
Reaction Steps
12-Chloro-dodec-5-yne (1 mmol) was mixed with potassium iodide (3 mmol) and 3,5-lutidine (3 mmol) in butanone. The mixture was refluxed for 3 days and cooled to room temperature, filtrated. The butanone was removed in vacuum, and the resulting residue was partitioned between water and ethyl ether. The aqueous layer was washed extensively with ether until no 3,5-lutidine was left in the aqueous layer. The resulting aqueous solution of the product was extracted with chloroform. The chloroform was removed to afford the product (78%). 1HNMR (300 MHz, CDCl3, ppm), 9.06 (s, 2H), 8.00 (s, 1H), 4.86 (t, 3H), 2.48 (s, 3H), 1.98-2.16 (m, 6H), 1.32-1.48 (br, 10H), 0.88 (t, 3H); 13CNMR, 146.12, 141.38, 138.64, 80.43, 79.53, 61.46, 31.70, 31.17, 28.68, 28.07, 25.55, 21.92, 18.57, 18.42, 13.63.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846937B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-e8b35a5adc1647c7bd588bcf180338f9 |
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| Source note | uspto-grants-2014_09 |
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