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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304778Generated: November 2, 2026

Toluene → Benzanilide

https://huagongshe.com/reaction/2304778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantHexaneHCID 8058—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14174668HCID 14174668—
CatalystHCID 131723444HCID 131723444—
SolventDiethyl EtherHCID 3283—
ProductBenzanilideHCID 716873%

Reaction Steps

Trimetyl alminum (0.98M n-hexane solution, 1.3 ml, 1.3 mmol) was added to an anhydrous toluene solution (2 ml) of N-allyl-N-benzoyl aniline (100 mg, 422 mmol) and nickel dichloro bis (diphenyl phosphino) propane (9 mg, 17 mmol) under ice cooling, and the mixture was refluxed for 7 hours. After the reaction, diethyl ether (3 ml) and a 0.5N solution (1.3 ml) of sodium hydroxide were added under ice cooling, and the mixture was stirred at room temperature for 2 hours. The reaction solution was dried over anhydrous magnesium sulfate, cerite was added thereto, the mixture was filtered, and the solvent was distilled away from the filtrate in vacuo. The resulting residue was subjected to silica gel chromatography (elution solution: diethyl ether/n-hexane=1/5, v/v) to N-benzoyl aniline (61 mg, yield 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437133B1
Source datasetuspto-grants-2002_08
ORD IDord-6c893c3b3a5a4deb9c753b0cb72fa2cf
Source noteuspto-grants-2002_08