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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl ethoxyacetate | HCID 69955 | — |
| Edukt | 2-Methyl-1,3,4-oxadiazole | HCID 558447 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethoxymethyl 5-methyl-1,3,4-oxadiazol-2-yl ketone | HCID 67323831 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08754099B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-6fa059c989d04a55b66333cae6dca4f2 |
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| Quellennotiz | uspto-grants-2014_06 |
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