HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 5-methyl-1,3,4-oxadiazole-2-carboxylate → Potassium 5-methyl-1,3,4-oxadiazole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 5-methyl-1,3,4-oxadiazole-2-carboxylate | HCID 13407467 | — |
| Reactant | Potassium trimethylsilanolate | HCID 23668039 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Potassium 5-methyl-1,3,4-oxadiazole-2-carboxylate | HCID 24820502 | 109.1% |
Reaction Steps
To a slurry of potassium trimethylsilanolate (411 mg, 3.20 mmol) in ether stirring at rt, was added in one portion ethyl 5-methyl-1,3,4-oxadiazole-2-carboxylate (0.50 g, 3.20 mmol). Immediate precipitation was observed with the color changing from white to off-white. The precipitate was removed by filtration, was washed with ether and dried to give the title compound as an off-white solid (580 mg, quantitative yield). 1H NMR (300 MHz, CDCl3): δ 2.61 (3H, s). 13C NMR (75 MHz, D2O): δ 166.7, 161.3, 159.3, 10.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687509B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-06921cf071c745c5bbefe14c68b883d3 |
| Source note | uspto-grants-2010_03 |