HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 2-(3-Ethoxyphenyl)-5H-[1,2,4]triazolo[5,1-a]isoindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 21455283 | HCID 21455283 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(3-Ethoxyphenyl)-5H-[1,2,4]triazolo[5,1-a]isoindole | HCID 134451 | 73% |
Reaction Steps
2-(3-Hydroxyphenyl)-5H-s-triazolo[5,1-a] isoindole (1.25 g, 0.05 mole) is added to 20 ml of ethanol containing one equivalent proportion of sodium ethoxide. To this mixture is added 0.49 ml (0.06 mole) of ethyl iodide in 5 ml of ethanol. After stirring for one hour at room temperature, a further amount of 0.49 ml of ethyl iodide is added. After refluxing for one hour the solvent is distilled off and the residue is washed with water and extracted with dichloromethane. Evaporation of the solvent and crystallization of the residue from ethanol gives 1 g (73%) of the title product, m.p. 166°-7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04007276 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-410221a369704c02b3a1f49c9d41d587 |
| Source note | uspto-grants-1977_02 |