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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714716Generated: October 31, 2026

2-Iodotoluene → Indane-5-yl-p-tolylamine

https://huagongshe.com/reaction/1714716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodotolueneHCID 5128—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
ReactantN-(2,3-Dihydro-1H-inden-5-yl)acetamideHCID 583823—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventIsoamyl AlcoholHCID 31260—
ProductIndane-5-yl-p-tolylamineHCID 1530987596.4%

Reaction Conditions

Temperature200 °C

Reaction Steps

5-(N-Acetylamino)indane (26.28 g (0.15 mol)), 43.61 g (0.20 mol) of iodotoluene, 25.88 g (0.188 mol) of anhydrous potassium carbonate and 2.38 g (0.038 mol) of copper powder were mixed, and heated up to 200° C. while introducing nitrogen gas, followed by stirring for 6 hours. After the termination of the reaction, cooling was conducted, and 22.3 g of potassium hydroxide dissolved in 20 ml of water and 50 ml of isoamyl alcohol were added to perform hydrolysis at 130° C. for 2 hours. After the termination of the hydrolysis, 250 ml of water was added, and isoamyl alcohol was removed by azeotropic distillation. Then, 200 ml of toluene was added to dissolve the reaction product. After filtration, dehydration was performed with magnesium sulfate. After magnesium sulfate was removed by filtration, the filtrate was concentrated, and purified by column chromatography (carrier: silica gel, eluent: toluene:hexane=1:4) to obtain 32.3 g of indane-5-yl-p-tolylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799492B2
Source datasetuspto-grants-2010_09
ORD IDord-a6db37ab49dd44b4813a92f0d43a214c
Source noteuspto-grants-2010_09