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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 406274Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/406274

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl ethoxyacetateHCID 69955—
Edukt2-Methyl-1,3,4-oxadiazoleHCID 558447—
EduktButyllithiumHCID 178418339—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthoxymethyl 5-methyl-1,3,4-oxadiazol-2-yl ketoneHCID 67323831—

Reaktionsbedingungen

Temperatur-40 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754099B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-6fa059c989d04a55b66333cae6dca4f2
Quellennotizuspto-grants-2014_06