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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505961Generated: November 2, 2026

Iodine → HCID 58266412, compound

https://huagongshe.com/reaction/1505961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant5-Bromo-6-chloropyridine-3-carboxylic acidHCID 285433—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58266412HCID 5826641253.1%

Reaction Conditions

Temperature-20 °C

Reaction Steps

n-Butyllithium (1.6M in hexanes, 172 mL, 276 mmol) was added to a solution of 2,2,6,6-tetramethylpiperidine (48.5 mL, 285 mmol) in anhydrous THF (200 mL) at −50° C. After 20 min, solid 5-bromo-6-chloronicotinic acid (21.6 g, 92 mmol) was added portionwise and the resultant slurry was allowed to warm to −20° C. over 1 h and stirred at that temperature for 1 h. After this time, the reaction mixture was cooled to −60° C. and transferred via cannula to a solution of iodine (70 g, 276 mmol) in anhydrous THF (100 mL) at −60° C. at such a rate that the internal temperature of the solution remained below −40° C. On complete addition, the reaction mixture was allowed to warm slowly to ambient temperature and stirred for 18 h. The reaction mixture was concentrated in vacuo and the resultant dark red slurry was dissolved in water (500 mL) and washed with diethyl ether (3×200 mL). The pH of aqueous layer was adjusted to 2 by the addition of 1M aqueous hydrochloric acid and the resulting beige precipitate was collected by filtration and dried under vacuum to afford the title compound (17.7 g, 53%). 1H NMR (DMSO-D6, 400 MHz): 8.30 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-e0a90c387a294f72ab614d150efdd825
Source noteuspto-grants-2015_12