Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 1-(2-Chloroethyl)-1,3-dihydro-2H-benzimidazol-2-one | HCID 3653471 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13105519 | HCID 13105519 | — |
Reaction Steps
A mixture of 70.4 parts of 1-(phenylmethyl)piperazine, 39.4 parts of 1-(2-chloroethyl)-1,3-dihydro-2H-benzimidazol-2-one and 360 parts of methylbenzene is stirred and refluxed overnight. The reaction mixture is cooled, water is added and the layers are separated. The methylbenzene-phase is washed three times with water, dried, filtered and evaporated. The solid residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is boiled in 2,2'-oxybispropane. The whole is cooled on an ice-bath. The product is filtered off and crystallized from a mixture of 2,2'-oxybispropane and a small amount of 2-propanol, yielding 1,3-dihydro-1-{2-[4-(phenylmethyl)-1-piperazinyl]ethyl}-2H-benzimidazol-2-one; mp. 136.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04377578 |
|---|
| Source dataset | uspto-grants-1983_03 |
|---|
| ORD ID | ord-9024d18aa51048febaaf4f85938a4257 |
|---|
| Source note | uspto-grants-1983_03 |
|---|