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HRID 1625192作成日:2026年10月27日

O-(4-Nitrophenyl)hydroxylamine → (2-Butyl-5-nitrobenzofuran-3-yl)(4-methoxyphenyl)methanone

https://huagongshe.com/reaction/1625192

反応式

関与物質

役割名称HCID仕込み量
反応物O-(4-Nitrophenyl)hydroxylamineHCID 15562106—
反応物1-(4-Methoxyphenyl)-heptane-1,3-dioneHCID 44541818—
溶媒Acetic AcidHCID 176—
生成物(2-Butyl-5-nitrobenzofuran-3-yl)(4-methoxyphenyl)methanoneHCID 2259505570%

反応条件

温度70 °C

反応手順

O-4-nitrophenylhydroxylamine (100 mg), was suspended in 0.5 ml acetic acid and 1-(4-methoxyphenyl)-heptane-1,3-dione was added. The mixture was stirred at 70° C. for 3 h and then at 100° C. for an additional 14 h. The mixture was cooled to room temperature and the solvent evaporated under vacuum. Yield 70% of 2-butyl-3-(4-methoxybenzoyl)-5-nitrobenzofuran.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08779201B2
出典データセットuspto-grants-2014_07
ORD IDord-3c7a7e1806bd48a19f946c7756e4e421
出典メモuspto-grants-2014_07