HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → 4,5-Dihydrotetrazolo[1,5-a]quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | HCID 10103592 | HCID 10103592 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,5-Dihydrotetrazolo[1,5-a]quinoxaline | HCID 21514049 | 45% |
Reaction Steps
A 1 g. portion of tetrazolo[1,5-a]quinoxaline was dissolved in 200 ml. of ethanol. The solution was placed in a Parr hydrogenator on a shaking apparatus and 100 mg. of 5 percent palladized charcoal was added. The bomb was pressurized to about 2 atmospheres with hydrogen and was shaken for 2 hours. The reaction mixture was then removed and filtered. The filtrate was evaporated to dryness and the residue was recrystallized from ethanol-water to obtain the product, 4,5-dihydrotetrazolo[1,5-a]quinoxaline, m.p. 149°-51°C., in 45 percent yield. The product was identified by nuclear magnetic resonance analysis and by elemental microanalysis, with the following results.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03979387 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-bd0f956c3b6b459aaedcceb9ea95ca2e |
| Source note | uspto-grants-1976_09 |