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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 340423Erstellt: 24. Oktober 2026

Iodine → tert-Butyl (6-chloro-4-iodopyridin-3-yl)carbamate

https://huagongshe.com/de/reaction/340423

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktWaterHCID 962—
Edukt(6-Chloro-pyridin-3-yl)-carbamic acid tert-butyl esterHCID 7330593—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-Butyl (6-chloro-4-iodopyridin-3-yl)carbamateHCID 5341532032,3%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To the solution of tert-butyl (6-chloropyridin-3-yl)carbamate (160 g, 0.7 mol) in 1 L of anhydrous THF was added n-BuLi (600 mL, L5 ml) at −78° C. under N2 atmosphere. After the addition was finished, the solution was stirred at −78° C. for 30 min, and the solution of I2 (177.68 g, 0.7 mol) in 800 mL of anhydrous THF was added. Then the solution was stirred at −78° C. for 4 hrs, TLC indicated the reaction was over. Water was added for quench, and EtOAc was added to extract twice. The combined organic phases were washed with brine, dried over Na2SO4, filtered and purified by flash chromatography to afford 80 g of tert-butyl (6-chloro-4-iodopyridin-3-yl)carbamate as a yellow solid (32.3%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895586B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-051484aadb5545ff80213495b030f72d
Quellennotizuspto-grants-2014_11