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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600343Generated: November 2, 2026

Toluene → HCID 15538105, compound

https://huagongshe.com/reaction/1600343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantAnilineHCID 6115—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 15538104HCID 15538104—
SolventEthyl AcetateHCID 8857—
ProductHCID 15538105HCID 15538105—

Reaction Steps

To Diphenylphosphoryl azide (5.75 g) in anhydrous toluene (50 mL) at 100° C. under nitrogen was added dropwise a solution containing Ethyl-3-nitro-4-carboxybenzoate (5 g) and triethylamine (4 mL) in anhydrous toluene (50 mL). The mixture was stirred for 1 h followed by theaddition of aniline (5 mL), and the reaction was allowed to cool to room temperature (40 min). Ethyl acetate (300 mL) was added and the solution was washed successively with 1N HCl (300 mL), water (300 mL), 1N NaOH (300mL) and water (300 mL). The organic layer was dried and the solvent was removed in vacuo. To the resulting oil was added diethyl ether (50 mL), and the resulting solid was collected and dried yielding N-(2-Nitro-5-methylphenyl)-N'-phenyl-urea as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05744602
Source datasetuspto-grants-1998_04
ORD IDord-7c7593ea425d47a4ace84df9dd16fa8b
Source noteuspto-grants-1998_04