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HRID 378968作成日:2026年10月26日

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

https://huagongshe.com/reaction/378968

反応式

関与物質

役割名称HCID仕込み量
反応物5-(2-nitrophenyl)-3H-1,3,4-oxadiazol-2-oneHCID 312921—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物5-(2-Aminophenyl)-1,3,4-oxadiazol-2(3H)-oneHCID 1285814893.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06297261B1
出典データセットuspto-grants-2001_10
ORD IDord-f78aa3592ecc4746adebbabc51b8c5ee
出典メモuspto-grants-2001_10