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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2121748생성일: 2026년 10월 25일

5-(2-nitrophenyl)-3H-1,3,4-oxadiazol-2-one → 5-(2-Aminophenyl)-1,3,4-oxadiazol-2(3H)-one

https://huagongshe.com/reaction/2121748

반응식

참여 물질

역할이름HCID투입량
반응물5-(2-nitrophenyl)-3H-1,3,4-oxadiazol-2-oneHCID 312921—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물5-(2-Aminophenyl)-1,3,4-oxadiazol-2(3H)-oneHCID 1285814893.1%

반응 단계

A solution of 2-nitrobenzoylhydrazine (9.05 g, 0.05 mol) in dioxane (30 mL) was slowly added to a solution of trichloromethyl chloroformate (4.6 mL, 0.04 mol) in dioxane (30 mL) at room temperature. On completion of the addition the reaction was heated to reflux for 4 hours. The solvent was evaporated off and the residue re-crystallised from 96% ethanol (50 mL) to give 7.15 g of the 5-(2-nitrophenyl)-3H-[1,3,4]oxadiazol-2-one. M.p. 157-158° C. A solution of the nitro compound (2 g, 9.7 mmol) in 96% ethanol (25 mL) was hydrogenated over 5% palladium on charcoal to give desired 1.6 g of the desired amine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06696475B2
출처 데이터셋uspto-grants-2004_02
ORD IDord-7c3f7ce3f7284aa99eff46be58c367b4
출처 메모uspto-grants-2004_02