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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340423Generated: October 27, 2026

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

https://huagongshe.com/reaction/340423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
Reactant(6-Chloro-pyridin-3-yl)-carbamic acid tert-butyl esterHCID 7330593—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl (6-chloro-4-iodopyridin-3-yl)carbamateHCID 5341532032.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895586B2
Source datasetuspto-grants-2014_11
ORD IDord-051484aadb5545ff80213495b030f72d
Source noteuspto-grants-2014_11