HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 7-(1-Bromoethyl)-1,2,4-triazolo[1,5-a]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-Ethyl-1,2,4-triazolo[1,5-a]pyrimidine | HCID 18919353 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 7-(1-Bromoethyl)-1,2,4-triazolo[1,5-a]pyrimidine | HCID 18919351 | — |
Reaction Steps
A mixture of 7-ethyl-1,2,4-triazolo[1,5-a]pyrimidine (10.5 g), N-bromosuccinimide (12.63 g), dibenzoylperoxide (0.3 g) and tetrachloromethane (270 ml) was heated under reflux for 5 hours with stirring. The mixture was filtered and a crude product was obtained by evaporation of the solvent from the filtrate. This was purified by recrystallisation from tetrachloromethane to give 7-(1-bromoethyl)-1,2,4-triazolo[1,5-a]pyrimidine. Yield 10.8 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753665 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-500a3da8126445c6a19de442eeceb3b4 |
| Source note | uspto-grants-1998_05 |