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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580322Generated: November 3, 2026

Toluene → N'-(2-chlorocyclohexyl)-urea

https://huagongshe.com/reaction/1580322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantN-(aminocarbonyl)benzenesulphonamideHCID 118791—
Reactant2-Chlorocyclohexan-1-amineHCID 418800—
SolventAcetic AcidHCID 176—
ProductN'-(2-chlorocyclohexyl)-ureaHCID 85911145—

Reaction Steps

A mixture of 10.3 g of of N-[4-<2-methoxy-5-chlorobenzamido>-ethyl)-benzenesulfonyl]-ethyl)-benzenesulfonyl-urea (melting point 171° -173°C), 300 ml of toluene, 30 ml of glycolmonomethyl-ether, 1.65 g of glacial acetic acid and 3.3 g of 2-chloro-cyclohexylamine are heated under reflux for 5 hours. Then the whole is concentrated in vacuo and the residue is treated with alcohol. The N-[4-(β<2-methoxy-5-chlorobenzamido> -ethyl)-benzenesulfonyl]-N'-(2-chlorocyclohexyl)-urea obtained as crude product melts at 194° -195°C after recrystallization from methanol/dimethylformamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03932503
Source datasetuspto-grants-1976_01
ORD IDord-2336f2a4baa044938270d14e125c5e92
Source noteuspto-grants-1976_01