HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → HCID 21484225, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | 2-Aminobenzimidazole | HCID 13624 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 21484225 | HCID 21484225 | 32.2% |
Reaction Steps
A mixture of 13.3 g of 2-aminobenzimidazole, 18.5 g of 2-phenylethyl bromide, and 300 ml of xylene is heated as in Example 1. Subsequently, the solution is concentrated to dryness, the residue is dissolved in boiling acetonitrile, and clarified by filtration. The crystalline product that separates in the cooled filtrate is filtered to give 6.8 g of 1,3-dihydro-1,3-bis(2-phenylethyl)-2H-benzimidazol-2-imine hydrobromide, m.p. 259°-260°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04004016 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-79500d224bd843af8e86b2012bb3cd80 |
| Source note | uspto-grants-1977_01 |