HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → 5-Methyl-2-(4-(4-methylphenyl)-3-thienyl)-[1,3,4]oxadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178423922 | HCID 178423922 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Methyl-2-(4-(4-methylphenyl)-3-thienyl)-[1,3,4]oxadiazole | HCID 18968902 | — |
Reaction Steps
A mixture of 5-(4-(4-methylphenyl)-3-thienyl)-tetrazole (3.3 g, 13.2 mmol) and acetic anhydride (50 ml) was heated at reflux temperature for 1 h. The resulting solution was evaporated in vacuo to give an oily residue which was dissolved into ethyl acetate (100 ml). The organic solution was vashed with a sodium bicarbonate solution (100 ml), treated with activated charcoal and dried (MgSO4). Filtration and evaporation in vacuo afforded 3.4 g of 5-methyl-2-(4-(4-methylphenyl)-3-thienyl)-[1,3,4]- oxadiazole as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05817654 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-81765c7f64d4451c9f42fbbca691c5ab |
| Source note | uspto-grants-1998_10 |