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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414913Generated: October 29, 2026

Water → 1-Tert-butyl-3-(3-oxo-1-cyclohexene-1-yl)urea

https://huagongshe.com/reaction/1414913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,3-CyclohexanedioneHCID 10434—
Reactant(1,1-Dimethylethyl)ureaHCID 14233—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
Product1-Tert-butyl-3-(3-oxo-1-cyclohexene-1-yl)ureaHCID 2148605566.7%

Reaction Steps

To a solution of 11.2 g of 1,3-cyclohexanedione in 250 ml of benzene is added 11.6 g tert-butylurea and 100 mg of p-toluenesulfonic acid. The solution is heated at reflux under nitrogen with water removal for three hours. At the end of this period the solution is cooled and the precipitated product removed by filtration. The precipitate is recrystallized from acetonitrile to give 14 g of 1-tert-butyl-3-(3-oxo-1-cyclohexene-1-yl)urea, m.p. 223°-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04002767
Source datasetuspto-grants-1977_01
ORD IDord-8431755f137a43b69ed8b570e3c7ee3b
Source noteuspto-grants-1977_01