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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771610Generated: November 3, 2026

Hydrochloric Acid → 2-Fluoro-3-iodo-5-methoxybenzoic acid

https://huagongshe.com/reaction/1771610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant2-Fluoro-5-methoxybenzoic acidHCID 2774543—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-3-iodo-5-methoxybenzoic acidHCID 8944412816%

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a solution of 2,2,6,6-tetramethylpiperidine (42 g, 298 mmol, 2.5 eq) in THF at −60° C. under N2 was added n-BuLi (2.2 M, 141 mL, 309.3 mmol, 2.6 eq) dropwise over a period of 30 min. The reaction mixture was stirred at −60° C. for 2 h, then a solution of 2-fluoro-5-methoxy-benzoic acid (15 g, 119 mmol, 1.0 eq) in THF (300 mL) was added dropwise with stirring. The reaction was stirred for a further 2 h at −60° C., then iodine (45 g, 179 mmol, 1.5 eq) was added in portions. The reaction was warmed to room temperature slowly and the resulting mixture acidified by addition of 1M HCl and extracted with EtOAc. The organic extract was washed with water and brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue was purified by column chromatography (EtOAc:petroleum ether, 0:1 to 1:1) to give the title compound as a yellow solid (5.6 g, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249085B2
Source datasetuspto-grants-2016_02
ORD IDord-6e794a9129f14f1fa07db19bd41e78d4
Source noteuspto-grants-2016_02