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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518405Generated: October 25, 2026

Iodine → 4-Iodo-6-methylsulfonylpyridin-3-ol

https://huagongshe.com/reaction/518405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
Reactant6-(Methylsulfonyl)pyridin-3-olHCID 23145196—
SolventTetrahydrofuranHCID 8028—
Product4-Iodo-6-methylsulfonylpyridin-3-olHCID 118022024—
Product2-Iodo-6-methylsulfonylpyridin-3-olHCID 118022372—

Reaction Steps

A mixture of the title compound from Step 1 (3.0 g, 17.34 mmol), I2 (6.6 g, 26.01 mmol), NaHCO3 (2.2 g, 26.20 mmol) and KI (0.72 g, 4.34 mmol) in THF (30 mL) and H2O (30 mL) was stirred at 60° C. for 18 hrs. Water (100 mL) was added and the mixture was extracted with EtOAc (100 mL×3). The combined organic layers were washed with brine (100 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by preparative HPLC to give 4-iodo-6-methylsulfonylpyridin-3-ol (700.0 mg) and 2-iodo-6-methylsulfonylpyridin-3-ol (700.0 mg). 2-iodo-6-methylsulfonylpyridin-3-ol: 1H NMR (CDCl3, 400 MHz) δ 12.08 (brs, 1H), 7.86 (d, J=8.4 Hz, 1H), 7.31 (d, J=8.4 Hz, 1H), 3.19 (s, 3H). 4-iodo-6-methylsulfonylpyridin-3-ol: 1H NMR (CDCl3, 400 MHz) δ 12.0 (brs, 1H), 8.24 (s, 1H), 8.17 (s, 1H), 3.20 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115114B2
Source datasetuspto-grants-2015_08
ORD IDord-542ace4993ea452dac80a938285196db
Source noteuspto-grants-2015_08