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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968254Generated: October 29, 2026

Iodine → 5-fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde

https://huagongshe.com/reaction/1968254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium IodideHCID 5238—
ReactantSodium HydroxideHCID 14798—
Reactant1H-Pyrrolo[2,3-b]pyridine-4-carboxaldehyde, 5-fluoro-HCID 49761623—
SolventEthanolHCID 702—
SolventSodium BisulfiteHCID 23665763—
Product5-fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine-4-carbaldehydeHCID 86654207151%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 5-fluoro-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde (2.45 g, 14.93 mmol) in EtOH (20 mL) was added iodine (4.55 g, 17.91 mmol), sodium iodide (2.68 g, 17.91 mmol) and aqueous NaOH (1N, 15 mL). The reaction mixture was stirred for 4 h at 25° C. and diluted with aqueous NaHSO3 (0.1N). An orange precipitate was collected by filtration and dried under vacuum to afford the title compound as a yellow solid (6.54 g, 82%). [M+H] calc'd for C8H4F1N2O, 291; found, 291.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420816B2
Source datasetuspto-grants-2013_04
ORD IDord-4e2fb422f9cf464981dd4d9da251d01d
Source noteuspto-grants-2013_04