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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865093Generated: October 31, 2026

Water → 1-Fluoro-2-(4-iodophenoxy)benzene

https://huagongshe.com/reaction/1865093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiiodomethaneHCID 6346—
ReactantIsoamyl NitriteHCID 8053—
Reactant4-(2-Fluorophenoxy)anilineHCID 5126073—
SolventAcetonitrileHCID 6342—
Product1-Fluoro-2-(4-iodophenoxy)benzeneHCID 5797531891.7%

Reaction Conditions

Temperature55 °C

Reaction Steps

Add isoamylnitrite (2.45 g, 2.5 Eq.) to 4-(2-fluoro-phenoxy)-phenylamine (1.70 g, 8.37 mmol) and diiodomethane (7.84 g, 3.5 Eq.) in acetonitrile (10 mL) while stirring at 55° C. under a nitrogen atmosphere. Slowly heat mixture to 75° C. and heat at this temperature for 3 hours. Cool to room temperature and pour into water, and extract the desired material into ethyl acetate. Wash this organic layer once with water, dry over potassium carbonate, filter, and concentrate under reduced vacuum to give 2.41 g of an oil. Purify the material by silica gel chromatography (Prep. 2000) eluting with hexane/methylene chloride 9:1 to provide 1.60 g of the title compound as a thin oil. Mass spectrum (m/e): 314.0 (M*): (Bruker 300) 1H NMR (CDCl3) δ 7.55-7.60 (2H, d), 7.02-7.20 (4H, m), 6.69-6.72 (2H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625932B2
Source datasetuspto-grants-2009_12
ORD IDord-d95faa6f97484b5caa8751cd09b15e67
Source noteuspto-grants-2009_12