HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene, (triethoxymethyl)- → 4-Chloro-1-phenyl-[1,2,4]triazolo[4,3-a]quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene, (triethoxymethyl)- | HCID 74268 | — |
| Reactant | 2-Chloro-3-hydrazinoquinoxaline | HCID 3658820 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Chloro-1-phenyl-[1,2,4]triazolo[4,3-a]quinoxaline | HCID 899290 | — |
Reaction Steps
2-Chloro-3-hydrazinoquinoxaline (2.2 g., 0.011 mole) was mixed with 6 ml. of triethyl orthobenzoate and heated at 100° C. for 30 minutes. After cooling the orange mixture to room temperature, ethanol was added. Filtration of the resultant precipitate afforded 2.1 g. of crude product which was further purified by means of trituration with warm methanol, followed by filtration and air drying to ultimately yield 1.58 g. (51%) of pure 4-chloro-1-phenyl-[1,2,4]triazolo[4,3-a]quinoxaline as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04547501 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-115b1a55758241a79305b5a4ab1f0ffc |
| Source note | uspto-grants-1985_10 |