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HRID 704468作成日:2026年10月26日

Dimethylformamide → 4-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)nitrobenzene

https://huagongshe.com/reaction/704468

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物Acetic acid, chloro-, pentyl esterHCID 138488—
反応物Phenol, 2-chloro-4-fluoro-5-nitro-HCID 158655—
溶媒WaterHCID 962—
生成物4-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)nitrobenzeneHCID 1461784977.3%

反応条件

温度50 °C

反応手順

A mixture of 2-chloro-4-fluoro-5-nitrophenol (100 g), anhydrous potassium carbonate (86.6 g) and dimethylformamide (500 g) was heated at 50° C., and amyl 2-chloroacetate (90.2 g) was dropwise added thereto in 30 minutes, followed by allowing to stand at 60° C. for 4 hours. The reaction mixture was cooled to room temperature, and water (1500 g) was added thereto, followed by extraction with ethyl acetate (1500 g). The organic layer was separated, washed with water and concentrated under reduced pressure. The residue was distilled under reduced pressure to give 4-chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)nitrobenzene (Compound (III)) (129 g) as a pale yellow oil. Yield, 77%. b.p., 160 °-165° C./0.7 mmHg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04987247
出典データセットuspto-grants-1991_01
ORD IDord-7d833a2fbac6442e9b55822269a7a13a
出典メモuspto-grants-1991_01