Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224151Generated: October 25, 2026

Cyclopropylamine → 1-(4-Bromophenyl)-3-cyclopropylurea

https://huagongshe.com/reaction/2224151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
Reactant4-Bromophenyl isocyanateHCID 75609—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Bromophenyl)-3-cyclopropylureaHCID 45860333100.1%

Reaction Steps

Under a nitrogen atmosphere, tetrahydrofuran (80 ml) was added to 4-bromophenyl isocyanate 30 (10.0 g), and a solution of cyclopropylamine 1 (3.17 g) in tetrahydrofuran (20 ml) was added dropwise with stirring under ice-cooling. After the completion of the dropwise addition, the mixture was stirred at room temperature for 3 hrs, and the reaction mixture was concentrated under reduced pressure. Diethyl ether-hexane [1:1 (volume ratio), 100 ml] was added to the residue and, after stirring, the crystals were collected by filtration and dried to give 1-(4-bromo-phenyl)-3-cyclopropyl-urea 31 (12.9 g, over weight) as colorless crystals, which were used for the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378423B2
Source datasetuspto-grants-2008_05
ORD IDord-7d6e004d1744481fa9fd4b6bbb516a8f
Source noteuspto-grants-2008_05