HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4,5-bis-(4-bromophenyl)-1H-imidazole-2-thione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 1,2-Bis(4-bromophenyl)-2-hydroxyethanone | HCID 3938243 | — |
| Solvent | 1-Hexanol | HCID 8103 | — |
| Product | 4,5-bis-(4-bromophenyl)-1H-imidazole-2-thione | HCID 3554615 | — |
Reaction Steps
A mixture of 4,4'-dibromobenzoin (25 g, 0.068 mol) and thiourea (10.3 g, 0.14 mol) in hexanol (200 ml) was refluxed with azeotropic distillation of water for three hours. The solution was then cooled and ethanol (300 ml) was added. The mixture was further cooled and the small needles which formed were collected and washed with cold ethanol then ether and dried. Recrystallization of the product from ethyl acetate gave 4,5-bis-(4-bromophenyl)-1H-imidazole-2-thione, m.p. 288°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04188397 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-923517e0f45c4bbea8b8ddf7c9c5cb19 |
| Source note | uspto-grants-1980_02 |