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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109352Generated: October 30, 2026

Benzene → HCID 15230361, compound

https://huagongshe.com/reaction/1109352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantUreaHCID 1176—
Reactant2,4-Dibromobutyryl chlorideHCID 4413143—
SolventEthyl AcetateHCID 8857—
ProductHCID 15230361HCID 1523036166.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 30 g of 2,4-dibromobutyryl chloride (J. Med. Chem., p1995, 30. 1987) and 13.63 g of urea dissolved into 150 ml of benzene was heated at 90° C. with stirring for 3 hours. The reaction mixture was cooled to room temperature, then a very excessive amount of ethyl acetate was added thereto. The layer of ethyl acetate was washed with an aqueous solution of sodium bicarbonate and saturated brine, then the resulting solution was dried over magnesium sulfate and evaporated. The obtained residue (28 g) was dissolved into 30 ml of tetrahydrofuran (THF) and cooled. To this mixture was added 4.7 g of NaH (55% in mineral oil) bit by bit, then the mixture was stirred at room temperature for 2 hours. The reaction mixture was evaporated to make the amount of the solution about 50 ml, then which was poured into ethyl acetate. The layer of ethyl acetate was washed with water and saturated brine, dried over magnesium sulfate, and evaporated. The obtained residue was washed well with n-hexane, whereby 15.7 g of the objective compound was obtained in 66% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05319099
Source datasetuspto-grants-1994_06
ORD IDord-c4dd482fd68f47068d615676e98c3fb8
Source noteuspto-grants-1994_06