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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596308Generated: October 28, 2026

Aniline → HCID 13018269, compound

https://huagongshe.com/reaction/596308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantN-[4-chlorobenzyl]-N-sec.-butyl-carbamoyl chlorideHCID 21452004—
SolventTolueneHCID 1140—
ProductHCID 13018269HCID 1301826983%

Reaction Steps

19 g (0.2 mole) of aniline were dissolved in 300 ml of toluene. To the resulting solution, a solution of 26 g (0.1 mole) of N-[4-chlorobenzyl]-N-sec.-butyl-carbamoyl chloride in 70 ml of toluene was added dropwise, under cooling and stirring. After the dropwise addition, the temperature of the solution was gradually raised, and the the solution was stirred at a temperature of 70°-80° C for about 5 hours. The solution was cooled to precipitate aniline hydrochloride, which was then separated by filtration. The toluene layer was washed with 100 ml of water and dried with anhydrous sodium sulfate. Then, the toluene was distilled off. The residue was subjected to recrystallization from a mixture of hexane and ethyl alcohol, whereby 26.3 g of N-(4-chlorobenzyl)-N-sec.-butyl-N'-phenylurea were obtained. Yield: 83%. Melting point: 80°-81.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04010281
Source datasetuspto-grants-1977_03
ORD IDord-8b0fd0eb184d4499a0e9b192cc33ca95
Source noteuspto-grants-1977_03