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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl ethoxyacetate | HCID 69955 | — |
| Reactant | 2-Methyl-1,3,4-oxadiazole | HCID 558447 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethoxymethyl 5-methyl-1,3,4-oxadiazol-2-yl ketone | HCID 67323831 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754099B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-6fa059c989d04a55b66333cae6dca4f2 |
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| Source note | uspto-grants-2014_06 |
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