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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654298Generated: October 25, 2026

Aniline → Carbanilide

https://huagongshe.com/reaction/654298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantNitrobenzeneHCID 7416—
ReactantTetramethylureaHCID 12437—
ReactantHCID 178418416HCID 178418416—
CatalystTriruthenium dodecacarbonylHCID 6096991—
SolventTolueneHCID 1140—
ProductCarbanilideHCID 759536.3%

Reaction Steps

Into a 200 ml autoclave equipped with a magnetic stirrer were introduced 5.6 g of nitrobenzene, 7.8 g of aniline, 27 ml of toluene, 6.3 g of N,N,N',N'-tetramethylurea (referred to hereafter as TMU), and 20 mg of Ru3 (CO)12. Thereafter the atmosphere within the system was changed to one of carbon monoxide, within was set at a pressure of 50 kg/cm2. Subsequently the reaction was carried out at 160° C. for 2 hours, with continuous stirring. After completion of the reaction, the system was cooled to room temperature, and following gas evacuation, the reaction liquor was filtered and 3.5 g of N,N'-diphenyl urea crystals obtained. The filtrate was analyzed by gas chromatography and high speed liquid chromatography, and found to contain 0.1 g of N,N'-diphenyl urea and 2.9 g of nitrobenzene. This indicated that the TOF (Turn Over Frequency) of N,N'-diphenyl urea production was 100 h-1 based on catalyst metal atoms, and the selectivity based on nitrobenzene was 94%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05130464
Source datasetuspto-grants-1992_07
ORD IDord-7c206bd084c24a868c2721b6bd500986
Source noteuspto-grants-1992_07