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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37291Generated: October 25, 2026

Pyridine → N-(2,6-diisopropylphenyl)-N'-(4-tert-butylcyclohexyl)urea

https://huagongshe.com/reaction/37291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-tert-ButylcyclohexylamineHCID 79396—
Reactant2,6-Diisopropylphenyl isocyanateHCID 92259—
SolventDichloromethaneHCID 6344—
ProductN-(2,6-diisopropylphenyl)-N'-(4-tert-butylcyclohexyl)ureaHCID 1993504159.5%

Reaction Steps

To a solution of 1.6 g of 4-tert-butylcyclohexylamine in 15 ml of dichloromethane was added a solution of 2.2 g of 2,6-diisopropylphenylisocyanate in dichloromethane dropwise in the presence of pyridine at 0° C. Thereafter the mixture was stirred for 1.5 hours at room temperature and concentrated. The residue was partitioned between isopropyl ether and water, and the organic layer was successively washed with 0.5N hydrochloric acid, water and sodium sulfate solution. The organic layer was dried over magnesium sulfate and then distilled away. The resulting residue was crystallized from ethyl acetate to give 2.2 g of N-(2,6-diisopropylphenyl)-N'-(4-tert-butylcyclohexyl)urea, melting at 270° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420164
Source datasetuspto-grants-1995_05
ORD IDord-6a6b231c3e824992b74412a4122da314
Source noteuspto-grants-1995_05