Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489907Generated: October 30, 2026

Iodine → 4-methoxy-2-methyl-N-phenylaniline

https://huagongshe.com/reaction/1489907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantFormanilideHCID 7671—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Bromo-4-methoxy-2-methylbenzeneHCID 117915—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-methoxy-2-methyl-N-phenylanilineHCID 162461—

Reaction Conditions

Temperature170 °C

Reaction Steps

12.1 g (0.1 mol) of formanilide, 22.1 g (0.11 mol) of 2-bromo-5-methoxytoluene of the formula (101), 13.8 g (0.1 mol) of anhydrous potassium carbonate, 2.0 g (0.0079 mol) of iodine and 1.6 g (0.025 mol) of copper powder are initially placed in a 100 ml sulfonating flask fitted with an anchor stirrer, thermometer, condenser and oil bath, and the mixture is stirred. It is heated to 170° C. and then stirred at 170° C. for 22 hours, to give a black melt. This melt is then cooled to 80° C., a little toluene is added, and the solution is filtered. The residue is rinsed with toluene. The toluene filtrate is distilled with steam spray (distillate: water/toluene/unreacted 2-bromo-5-methoxytoluene) to leave a residue which comprises a mixture of black oil and water. The black oil is boiled under reflux for 25 hours with 250 g of 50% potassium hydroxide solution. The product obtained is extracted with toluene and washed with hot water. The toluene phase is dried over sodium sulfate, filtered and concentrated. The residue which remains comprises 17.0 g of the compound of the formula ##STR12## as black crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679856
Source datasetuspto-grants-1997_10
ORD IDord-25b845b4587648b6b03371c5634a1ad1
Source noteuspto-grants-1997_10