HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Cyclopentylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Cyclopentylurea | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03932658 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-ea12b79f021d43b8bfd49fcd431891af |
| Source note | uspto-grants-1976_01 |