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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725734Generated: October 31, 2026

Acetanilide → (4-tert-Butyl-phenyl)-phenyl-amine

https://huagongshe.com/reaction/725734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetanilideHCID 904—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Bromo-4-tert-butylbenzeneHCID 77595—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
Product(4-tert-Butyl-phenyl)-phenyl-amineHCID 1144745958.9%

Reaction Steps

8.2 g (0.061 mol) of acetanilide, 19.2 g (0.090 mol) of p-tertiarybutylbromobenzene, 9.95 g (0.072 mol) of anhydrous potassium carbonate, and 0.50 g (0.008 mol) of copper powder were mixed. The reaction mixture was then allowed to undergo reaction at a temperature of 190° C. to 203° C. for 23 hours. The reaction product was then extracted with 75 ml of toluene. The insoluble contents were removed by filtration. The filtrate was then concentrated to dryness. The concentrate was then dissolved in 30 ml of isoamyl alcohol. The material was then hydrolyzed with 1.1 g of water and 7.9 g (0.12 mol) of 85% potassium hydroxide at a temperature of 125° C. The material was then subjected to steam distillation to distill off isoamyl alcohol and excess p-tertiarybutylbromobenzene. The residue was extracted with 80 ml of toluene, washed with water, and then concentrated to dryness. The concentrate was then recrystallized from 100 ml of n-hexane to obtain 8.1 g (yield: 58.9%) of N-phenyl-p-tertiarybutylaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05707747
Source datasetuspto-grants-1998_01
ORD IDord-d93696164b2e479393f10519ee991a31
Source noteuspto-grants-1998_01