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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587568Generated: October 26, 2026

4-Iodoanisole → 1-(4'-Methoxy-2-nitro-[1,1'-biphenyl]-4-yl)ethanone

https://huagongshe.com/reaction/1587568

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodoanisoleHCID 69676—
Reactant1-(4-Bromo-3-nitrophenyl)ethan-1-oneHCID 87737—
ReactantEthyl acetate hexaneHCID 21226206—
CatalystCopperHCID 23978—
SolventDichloromethaneHCID 6344—
Product1-(4'-Methoxy-2-nitro-[1,1'-biphenyl]-4-yl)ethanoneHCID 1895661636%

Reaction Conditions

Temperature80 °C

Reaction Steps

A stirred mixture of 4-iodoanisole (43.65 g, 0.187 mole), 4-bromo-3-nitro acetophenone (40.6 g, 0.166 mole) and copper powder (copper bronze, 36 g, 0.567 mole) kept under nitrogen is placed in an oil bath heated at 80° C. The temperature is slowly raised to 110° C. and the mixture is kept at this temperature for 5 days (TLC, 8:2 hexane-ethyl acetate). Upon cooling the mixture is dissolved in dichloromethane and filtered through a Celite pad. The filtrate and washing are evaporated and the residual thick, dark brown oil (58.4 g) is flash chromatographed (on silica Merck 60, preabsorbed in dichloromethane, eluted with 9:1 hexane-ethyl acetate to remove the impurities and 8:2 hexane-ethyl acetate to recover the main product) to provide 16.2 g (32%) of the title compound (yellow solid, m.p.124°-126° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05218124
Source datasetuspto-grants-1993_06
ORD IDord-cb65fa8e30dd4c53b70b57052b532707
Source noteuspto-grants-1993_06