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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194507Generated: November 2, 2026

Iodine → 2-Iodo-6-methoxynaphthalene

https://huagongshe.com/reaction/1194507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
Reactant2-Bromo-6-methoxynaphthaleneHCID 78786—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product2-Iodo-6-methoxynaphthaleneHCID 34906767.1%

Reaction Steps

To a solution of 1.00 g (4.22 mmol, Aldrich) of 6-bromo-2-methoxynaphthalene in 10 ml of dry THF at -78° was added dropwise 4.5 ml (1.4M in pentane, 6.3 mmol, Aldrich) of t-butyllithium solution over 10 minutes. The reaction mixture was stirred at -78° for 30 minutes then at 0° for 15 minutes. The resulting yellow solution was re-cooled to 31 78° then 1.20 g (4.72 mmol, Aldrich) of iodine was added in one portion. The reaction mixture was warmed to room temperature, stirred for 1 hour then added to 50 ml of H2O and extracted with 50 ml of ethyl acetate. The organic extract was washed with an additional 50 ml of H2O, dried (MgSO4) and concentrated in vacuo to give a solid. The crude solid was recrystallized (EtOAc/petroleum ether) to afford 805 mg (67%) of title compound as pale yellow flakes, m.p. 142°-143°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04814454
Source datasetuspto-grants-1989_03
ORD IDord-ee8b9dfa7a6c445e84a7dda10b1c066e
Source noteuspto-grants-1989_03