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HRID 1282083作成日:2026年10月25日

Ethanol → 2-Ethoxy-4-fluoronitrobenzene

https://huagongshe.com/reaction/1282083

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物5-Fluoro-2-nitrophenolHCID 9937—
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2-Ethoxy-4-fluoronitrobenzeneHCID 12918153—

反応手順

To a solution of ethanol (4.2 ml) in tetrahydrofuran (65 ml) was added a solution of triphenylphosphine (13 g) and 5-fluoro-2-nitrophenol (10 g) in tetrahydrofuran (65 ml). To this solution was added diethyl azodicarboxylate (10 ml) under ice-cooling and the mixture was stirred at room temperature for 4 hr. The reaction mixture was concentrated under reduced pressure and diisopropyl ether was added. The precipitated crystals were collected by filtration and concentrated under reduced pressure. The concentrate was subjected to silica gel column chromatography (developing solvent; hexane:ethyl acetate=4:1) to give a yellow oil. To this oil was added ethyl acetate, washed with an aqueous sodium hydroxide solution, dried over magnesium sulfate and concentrated under reduced pressure to give the title compound (9.6 g) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06455528B1
出典データセットuspto-grants-2002_09
ORD IDord-b9101ff535b44bc8a08ac03a994a6ea4
出典メモuspto-grants-2002_09