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HRID 1781906作成日:2026年10月26日

N'-[(3,4-dimethoxy-5-nitrobenzoyl)oxy]acetamidine → 5-(3,4-Dimethoxy-5-nitrophenyl)-3-methyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/1781906

反応式

関与物質

役割名称HCID仕込み量
反応物N'-[(3,4-dimethoxy-5-nitrobenzoyl)oxy]acetamidineHCID 53789064—
溶媒Acetic AcidHCID 176—
生成物5-(3,4-Dimethoxy-5-nitrophenyl)-3-methyl-1,2,4-oxadiazoleHCID 21459080—

反応手順

2.0 g of N'-[(3,4-dimethoxy-5-nitrobenzoyl)oxy] acetamidine are held at reflux temperature for 1 hour in 20 ml of glacial acetic acid. After distillation of the acetic acid, the crystalline residue is recrystallized from ether/hexane. There is obtained 5-(3,4-dimethoxy-5-nitrophenyl)-3-methyl-1,2,4-oxadiazole in the form of colorless crystals of m.p. 111°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05633371
出典データセットuspto-grants-1997_05
ORD IDord-f347339a177f4ab8a08748288e49560e
出典メモuspto-grants-1997_05