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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931857Generated: October 25, 2026

Iodine → 1-Bromo-4-iodonaphthalene

https://huagongshe.com/reaction/931857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1,4-DibromonaphthaleneHCID 66521—
ReactantSodium BisulfiteHCID 23665763—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-4-iodonaphthaleneHCID 5073667—

Reaction Conditions

Temperature-70 °C

Reaction Steps

100 g (350 mmol) of 1,4-dibromonaphthalene are initially introduced in 11 of THF, cooled to −70° C., and 235 ml of n-BuLi (1.6 M in hexane, 370 mmol) are added dropwise. After 1 h, 103 g (406 mmol) of I2 in 250 ml of THF are added dropwise, the mixture is stirred at −70° C. for a further 2 h, warmed to 0° C. and quenched by the addition of 50 ml (644 mmol) of aqueous NaHSO3 solution (w=39%). The phases are separated, and the aqueous phase is extracted once with MTB. The combined organic phases are washed with saturated sodium chloride soln., dried over sodium sulfate, filtered and evaporated in a rotary evaporator. The residue is purified by column chromatography (SiO2, heptane), and the further purification is carried out by recrystallisation from isopropanol, giving 1-iodo-4-bromonaphthalene as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296948B2
Source datasetuspto-grants-2016_03
ORD IDord-f0fbc23357924075aa3d1252886ca745
Source noteuspto-grants-2016_03