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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778653Generated: October 31, 2026

Potassium Iodide → 2,4-Difluoro-3-iodo-1,5-dimethoxybenzene

https://huagongshe.com/reaction/1778653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2,6-Difluoro-3,5-dimethoxybenzenamineHCID 10261892—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product2,4-Difluoro-3-iodo-1,5-dimethoxybenzeneHCID 8672280564.1%

Reaction Steps

To a stirred slurry of 2,6-difluoro-3,5-dimethoxyaniline (6.00 g, 31.7 mmol) in 6.0 M hydrogen chloride in water (54 mL, 324 mmol), a solution of sodium nitrite (2.30 g, 33.3 mmol) in water (12 mL) was added drop-wise over 15 min. at 0° C. After an additional 15 min., the result orange-red slurry was added to a solution of potassium iodide (21.0 g, 126 mmol) in water (30 mL) in small-portion at 0° C. The mixture was then allowed to stir at r.t. for 1 h. The precipitates were collected by filtration, washed with water, and dried under reduced pressure. The filtrate was neutralized with 6 N NaOH to pH˜7, and extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with saturated Na2S2O3 aqueous solution, dried over MgSO4, filtered and concentrated under reduced pressure. The residue combined with the precipitates collected previously was purified by flash chromatography on a silica gel column with ethyl acetate in hexanes (gradient: 0-50%) to afford the desired product (6.1 g, 64%). 1H-NMR (300 MHz, CDCl3): 6.68 (t, J=8.0 Hz, 1H), 3.88 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266892B2
Source datasetuspto-grants-2016_02
ORD IDord-51a7cc1f7d3441fbb86e44e0453ca7ab
Source noteuspto-grants-2016_02