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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580462Generated: October 27, 2026

Toluene → Cyclopentylurea

https://huagongshe.com/reaction/1580462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantUreaHCID 1176—
ReactantCyclopentylamineHCID 2906—
ReactantDiethyl EtherHCID 3283—
SolventAcetic AcidHCID 176—
ProductCyclopentylureaHCID 294526—

Reaction Steps

A mixture of 10.3 g of N-[4-(β-<2-methoxy-5-chlorobenzamido>-ethyl)-benzenesulfonyl]-urea (m.p. 171° - 173°C), 300 ml of toluene, 30 ml of glycolmonomethyl ether, 1.65 g of glacial acetic acid and 2.4 g of cyclopentyl-amine was refluxed for 5 hours. Subsequently, the mixture was concentrated in vacuo and the residue was treated with alcohol. N-[4-(β-<2-methoxy-5-chlorobenzamido>-ethyl)-benzenesulfonyl] -N'-cyclopentyl-urea obtained as a raw product was separated by suction-filtration and recrystallized from methanol. Melting point 184° - 185°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03932658
Source datasetuspto-grants-1976_01
ORD IDord-ea12b79f021d43b8bfd49fcd431891af
Source noteuspto-grants-1976_01