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HRID 967754作成日:2026年10月26日

Ethyl Acetate → 5-[(E)-2-phenylethenyl]-1,2,4-oxadiazole

https://huagongshe.com/reaction/967754

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
反応物HCID 178520452HCID 178520452—
溶媒HOAc dioxaneHCID 22565020—
生成物5-[(E)-2-phenylethenyl]-1,2,4-oxadiazoleHCID 222913428%

反応手順

N-[(Hydroxyamino)methylene]-cinnamamide (850 mg, 4.5 mmol) was dissolved in acetic acid/dioxane (20 mL 1:1 v:v), and heated to reflux for 2 h. The cooled solution was made basic (pH 8) with K2CO3, and partitioned between ethyl acetate and water. The organics were dried over Na2SO4, and concentrated in vacuo. The resultant solids were triturated with hot ethyl acetate, and the soluble portion was purified by flash column chromatography on silica eluting with 2:1 hexane:ethyl acetate to afford 5-[(E)-2-phenylethenyl]-1,2,4-oxadiazole (60 mg, 8% yield) as a white powder. M.p. 53–55° C. 1H NMR (CDCl3, 300 MHz) δ8.43 (s, 1H), 7.85 (d, J=16 Hz, 1H), 7.60 (m, 2H), 7.45 (m, 3H), 7.05 (d, J=16 Hz, 1H). MS (EI ionization) 171 (M+−H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06956049B1
出典データセットuspto-grants-2005_10
ORD IDord-6ad1428dd2c64d83a156f20351cef2f1
出典メモuspto-grants-2005_10