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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 967754생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/967754

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물HCID 178520452HCID 178520452—
용매HOAc dioxaneHCID 22565020—
생성물5-[(E)-2-phenylethenyl]-1,2,4-oxadiazoleHCID 222913428%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06956049B1
출처 데이터셋uspto-grants-2005_10
ORD IDord-6ad1428dd2c64d83a156f20351cef2f1
출처 메모uspto-grants-2005_10