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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282478Generated: October 25, 2026

p-Toluidine → Benzenamine, 2-methyl-N-(2-methylphenyl)-

https://huagongshe.com/reaction/1282478

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ToluidineHCID 7813—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Methylphenyl trifluoromethanesulphonateHCID 572481—
ReactantTrifluoromethanesulfonateHCID 2758875—
ReactantCy-vBRIDPHCID 12010824—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductBenzenamine, 2-methyl-N-(2-methylphenyl)-HCID 13642365%

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a reactor were introduced 0.503 g (2.10 mmol) of p-tolyl triflate and 4 mL of dioxane under a nitrogen atmosphere. The triflate was dissolved in the solvent. To this solution were added 0.246 g (2.29 mmol) of p-toluidine, 0.658 g (3.10 mmol) of potassium phosphate, 19.9 mg (2.1 mol % based on the triflate) of tris(dibenzylideneacetone)dipalladium, and 58.7 mg (7.2 mmol % based on the triflate) of the 1,1-diphenyl-2(dicyclohexylphosphino)propene obtained in Example 2. The resultant reaction mixture was stirred at 100° C. for 12 hours and then cooled. Saturated aqueous ammonium chloride solution was added thereto, and this mixture was extracted with toluene. The extract was dried with anhydrous magnesium sulfate. Thereafter, the solvent was removed under reduced pressure. The concentrate was purified by column chromatography to obtain 0.268 g (65%) of ditolylamine. The results obtained are shown in Table 20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455720B1
Source datasetuspto-grants-2002_09
ORD IDord-ee5445f5ddd04a17aed2e6d60f2922ab
Source noteuspto-grants-2002_09