Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 340478Erstellt: 24. Oktober 2026

Iodine → 2-Chloro-5-fluoro-4-iodopyridine

https://huagongshe.com/de/reaction/340478

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktSodium ThiosulfateHCID 24477—
Edukt2-Chloro-5-fluoropyridineHCID 2782801—
EduktLithium di-isopropylamideHCID 86591433—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelOxolane--water (1/1)HCID 21881883—
Produkt2-Chloro-5-fluoro-4-iodopyridineHCID 2482049546,7%

Reaktionsbedingungen

Temperatur-75 °C

Reaktionsschritte

A tetrahydrofuran (5 ml) solution containing 2-chloro-5-fluoropyridine (500 mg) was added to a tetrahydrofuran (20 ml) solution containing lithium-N,N-diisopropylamide (2M tetrahydrofuran/ethylbenzene/heptane solution) (2.9 ml) at −75° C. in a nitrogen atmosphere, followed by stirring at −75° C. for 3 hours. Subsequently, a tetrahydrofuran (5 ml) solution containing iodine (1.16 g) was added, followed by stirring at −75° C. for 1 hour. Then, water/tetrahydrofuran (2 ml/8 ml), water (10 ml), and 3M aqueous sodium thiosulfate were slowly added at −75° C., −50° C., and −35° C., respectively, to the reaction solution. The reaction solution was adjusted to room temperature, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=20:1 to 10:1), and a white solid of 2-chloro-5-fluoro-4-iodopyridine (457 mg) was thus obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895585B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-b1df6db62d3646958c54f88f02cbc85c
Quellennotizuspto-grants-2014_11