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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 84325Erstellt: 24. Oktober 2026

Sodium Iodide → 1-Dodec-7-ynyl-3,4-dimethyl-pyridinium iodide

https://huagongshe.com/reaction/84325

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
Edukt3,4-DimethylpyridineHCID 11417—
Edukt12-Chloro-5-dodecyneHCID 123509—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
Produkt1-Dodec-7-ynyl-3,4-dimethyl-pyridinium iodideHCID 2478125472%

Reaktionsschritte

12-Chloro-dodec-5-yne (1 mmol) was mixed with Sodium iodide (3 mmol) and 3,4-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 3,4-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 (72%). 1HNMR, (300 MHz, CDCl3, ppm, ppm), 9.22 (s, 1H), 9.04 (d, 1H), 7.80 (d, 1H), 4.84 (t, 3H), 2.52 (s, 3H), 2.50 (s, 3H), 1.92-2.14 (m, 6H), 1.28-1.45 (m, 10H), 0.84 (t, 3H). 13CNMR, 157.84, 143.39, 141.81, 138.53, 128.72, 80.80, 79.90, 61.23, 32.03, 31.54, 29.08, 28.48, 25.91, 22.30, 20.78, 18.96, 18.79, 17.44, 14.02.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846937B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-5e891cc7ab8f4e1186ceef63d022a235
Quellennotizuspto-grants-2014_09