Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355377Generated: October 31, 2026

2-Iodophenol → 1-(2-Iodophenoxy)-2-nitrobenzene

https://huagongshe.com/reaction/2355377

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodophenolHCID 10784—
ReactantPotassium CarbonateHCID 11430—
ReactantCesium fluorideHCID 25953—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
SolventDimethyl SulfoxideHCID 679—
Product1-(2-Iodophenoxy)-2-nitrobenzeneHCID 1127926693.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2-iodophenol (11.82 g, 52.7 mmol) and 1-fluoro-2-nitrobenzene (5.0 g, 35.1 mmol) in DMSO (50 mL was added K2CO3 (14.5 g, 105.3 mmol), followed by CsF (8.0 g, 52.7 mmol). The resulting suspension was stirred at 50° C. until no starting material remained (˜5 h), cooled to rt and partitioned between water (50 mL) and CH2Cl2 (50 mL). The water layer was separated and extracted with CH2Cl2 (2×10 mL). The combined organic layers were washed with 1 aq N NaOH (10 mL) and brine, and dried over Na2SO4. Solvent was removed under vacuum to give 1-(2-iodophenoxy)-2-nitrobenzene (11.2 g, 93%) as an oil, which was used for next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-2e8e1ceb28724a3abf2ada73a0e1e6d2
Source noteuspto-grants-2010_07