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HRID 38241作成日:2026年10月26日

3-Chlorophenol → 2-Chloro-1-(3-chlorophenoxy)-4-nitrobenzene

https://huagongshe.com/reaction/38241

反応式

関与物質

役割名称HCID仕込み量
反応物3-ChlorophenolHCID 7933—
反応物Cesium carbonateHCID 10796—
反応物2-Chloro-1-fluoro-4-nitrobenzeneHCID 67688—
溶媒acetonitrile N,N-dimethylformamideHCID 21891449—
生成物2-Chloro-1-(3-chlorophenoxy)-4-nitrobenzeneHCID 275207100%

反応手順

According to Scheme 3 Step 1, Method A: 2-Chloro-1-fluoro-4-nitrobenzene (1.12 mmol, 0.20 g) was added to a suspension of 3-chlorophenol (1.02 mmol, 0.10 mL), Cs2CO3 (1.25 mmol, 407 mg) in DMF/ACN (40:60, 3.6 mL). The reaction mixture was stirred at room temperature overnight. The reaction mixture was quenched with water. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over MgSO4, was filtered and was concentrated under reduced pressure. The crude product was used without further purification to obtain 2-chloro-1-(3-chlorophenoxy)-4-nitrobenzene (1.02 mmol, 288 mg, 100%) as an orange solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524726B2
出典データセットuspto-grants-2013_09
ORD IDord-b52fe3e2f3204a35b4cfbbf66d690716
出典メモuspto-grants-2013_09