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HRID 406274作成日:2026年10月26日

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

https://huagongshe.com/reaction/406274

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl ethoxyacetateHCID 69955—
反応物2-Methyl-1,3,4-oxadiazoleHCID 558447—
反応物ButyllithiumHCID 178418339—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物Ethoxymethyl 5-methyl-1,3,4-oxadiazol-2-yl ketoneHCID 67323831—

反応条件

温度-40 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754099B2
出典データセットuspto-grants-2014_06
ORD IDord-6fa059c989d04a55b66333cae6dca4f2
出典メモuspto-grants-2014_06