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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406274Generated: October 25, 2026

Ethyl ethoxyacetate → Ethoxymethyl 5-methyl-1,3,4-oxadiazol-2-yl ketone

https://huagongshe.com/reaction/406274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ethoxyacetateHCID 69955—
Reactant2-Methyl-1,3,4-oxadiazoleHCID 558447—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductEthoxymethyl 5-methyl-1,3,4-oxadiazol-2-yl ketoneHCID 67323831—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a stirred solution of the 2-methyl-1,3,4-oxadiazole (5.0 g, 59.5 mmol) in THF (100 mL) was added dropwise n-BuLi (23.79 mL, 59.5 mmol) in toluene under N2 at −78° C. After 1 h, ethyl ethoxyacetate (10.22 g, 77 mmol) was added. The reaction mixture was then allowed to warm to −40° C. and stirred for 2 h. The reaction mixture was then quenched with 65 mL of LON HCl and extracted with EtOAc. The organic layer was washed with water and then brine, dried over anhydrous Na2SO4, and concentrated. The resulting residue was purified on a flash chromatography column (Biotage™-40M) using a gradient of 0-100% of n-hexane/Et2O to give the desired product. 1H NMR (500 MHz, CD3OD): δ 1.27 (t, 3H), 2.64 (s, 3H), 3.69 (q, 2H), 4.88 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754099B2
Source datasetuspto-grants-2014_06
ORD IDord-6fa059c989d04a55b66333cae6dca4f2
Source noteuspto-grants-2014_06