HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Mercaptoethanol → HCID 15029144, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-(4-Bromophenyl)-2-(1H-1,2,4-triazol-1-yl)ethan-1-one | HCID 603161 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15029144 | HCID 15029144 | 15.3% |
Reaction Steps
To a slurry of 27.8 g 1-(4-bromophenyl)-2-(1H-1,2,4-triazol-1-yl) ethanone in 350 ml dry toluene and 175 ml 1-butanol were added 15.6 g 2-mercaptoethanol and 24.7 g p-toluenesulfonic acid. The mixture was refluxed under a Dean-Stark trap for 50 hours. After cooling, a white solid was removed by filtration and the filtrate evaporated. The residue was taken up in chloroform and washed twice with 10% aqueous sodium hydroxide and once with water. The organic layer was dried, filtered and evaporated to leave a liquid residue. The 1-butanol in the residue was removed azeotropically three times with cyclohexane leaving a slurry. The solid was isolated by filtration to give 5.2 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05545655 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-18a1d66947a943f98899bc9e3b00d4c7 |
| Source note | uspto-grants-1996_08 |