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HRID 403065作成日:2026年10月26日

Iodine → 1-Bromo-4-iodonaphthalene

https://huagongshe.com/reaction/403065

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物1,4-DibromonaphthaleneHCID 66521—
反応物Sodium BisulfiteHCID 23665763—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-Bromo-4-iodonaphthaleneHCID 5073667—

反応条件

温度-70 °C

反応手順

100 g (350 mmol) of 1,4-dibromonaphthalene are initially introduced in 1 l 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 of I2 (406 mmol) 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 solution, 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08747695B2
出典データセットuspto-grants-2014_06
ORD IDord-3d0b8e4d202d4c0daf61019d5cc40b59
出典メモuspto-grants-2014_06