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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant3,5-DimethylpyridineHCID 11565—
Reactant12-Chloro-5-dodecyneHCID 123509—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-Dodec-7-ynyl-3,5-dimethyl-pyridinium iodideHCID 2478125278%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846937B2
Source datasetuspto-grants-2014_09
ORD IDord-e8b35a5adc1647c7bd588bcf180338f9
Source noteuspto-grants-2014_09