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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879958Generated: October 27, 2026

Ethyl 5-methyl-1,3,4-oxadiazole-2-carboxylate → Potassium 5-methyl-1,3,4-oxadiazole-2-carboxylate

https://huagongshe.com/reaction/1879958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-methyl-1,3,4-oxadiazole-2-carboxylateHCID 13407467—
ReactantPotassium trimethylsilanolateHCID 23668039—
SolventDiethyl EtherHCID 3283—
ProductPotassium 5-methyl-1,3,4-oxadiazole-2-carboxylateHCID 24820502109.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318754B2
Source datasetuspto-grants-2012_11
ORD IDord-c7c15c2174d4487ca3342cd234d05adf
Source noteuspto-grants-2012_11