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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16232Generated: October 27, 2026

Cyclopentylamine → Cyclopentylurea

https://huagongshe.com/reaction/16232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
ReactantDichloromethaneHCID 6344—
ReactantTrimethylsilyl isocyanateHCID 70696—
SolventMethanolHCID 887—
ProductCyclopentylureaHCID 294526—

Reaction Steps

To a CH2Cl2 solution of cyclopentylamine was added trimethylsilyl isocyanate. The reaction mixture was stirred overnight. To this was added 200 ml of CH3OH, and the mixture was stirred for another 2 hrs. The reaction mixture was concentrated and was titrated using diethyl ether to give an off-white precipitate. The precipitate was filtered through a Buchner funnel to give cyclopentyl urea Compound 30a as a white crystalline solid compound (13.0 g, 86%). To this urea Compound 30a (5.0 g, 38.7 mmol) in acetic acid (11 mL), was added malonic acid (4.0 g, 38.7 mmol) followed by acetic anhydride (18 mL) and the reaction was stirred at 70° C. for 12 hrs. The reaction mixture was concentrated, cooled in an ice bath and titrated using 4/1 EtO2/EtOAc. A pale yellow crystalline solid precipitated out. The precipitate was filtered and washed 2-3 times using cold diethyl ether to obtain a pale yellow solid Compound 30b (2.5 g, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737155B2
Source datasetuspto-grants-2010_06
ORD IDord-fb620b1f1b874ecb900ab3ec42a331aa
Source noteuspto-grants-2010_06