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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414542Generated: October 27, 2026

Water → 1-(1,1-Dimethylbutyl)-3-(2,5-dihydro-5-oxo-3-furyl)urea

https://huagongshe.com/reaction/1414542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl 4-bromo-3-oxobutanoateHCID 295655—
Reactant1,1-DimethylbutylureaHCID 23341880—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
Product1-(1,1-Dimethylbutyl)-3-(2,5-dihydro-5-oxo-3-furyl)ureaHCID 214878908%

Reaction Steps

To a solution of 22 g of methyl-4-bromoacetoacetate in 200 ml benzene is added 14.4 g of 1,1-dimethylbutylurea and 100 mg of p-toluene sulfonic acid. The solution is heated at reflux under nitrogen for four hours with water removal. At the end of this period the solution is cooled and concentrated. The residual material is chromatographed on 400 g of silicic acid. Elution with a solution of benzene (60%), ethyl acetate (30%) and methanol (10%) gives crystalline material. Recrystallization of this material from ethyl acetate gives 1.8 g of 1-(1,1-dimethylbutyl)-3-(2,5-dihydro-5-oxo-3-furyl)urea, m.p. 130°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001425
Source datasetuspto-grants-1977_01
ORD IDord-d2e926817b9045e19496deef48436701
Source noteuspto-grants-1977_01