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HRID 547609作成日:2026年10月26日

4-Hydroxybenzyl Alcohol → {4-[(3,4-Dinitrophenyl)oxy]phenyl}methanol

https://huagongshe.com/reaction/547609

反応式

関与物質

役割名称HCID仕込み量
反応物4-Hydroxybenzyl AlcoholHCID 125—
反応物Cesium carbonateHCID 10796—
反応物Potassium CarbonateHCID 11430—
反応物3,4-DinitrofluorobenzeneHCID 298675—
溶媒DimethylformamideHCID 6228—
生成物{4-[(3,4-Dinitrophenyl)oxy]phenyl}methanolHCID 5758591045.2%

反応手順

4-fluoro-1,2-dinitrobenzene (20.0 g, 107.5 mmol), 4-(hydroxymethyl)phenol (14.7 g, 118.2 mmol) and potassium carbonate (17.8 g, 129.0 mmol) were stirred in 250 ml of dimethylformamide at room temperature for approximately 17 hours. The reaction was heated at 35 degree Centigrade for 1.5 hours. Cesium carbonate (2 g, 6.14 mmol) was added and the reaction was heated at 45 deg. C. for approximately 22 hours. The solids were filtered away and washed with ethyl acetate. The filtrate was diluted with water and extracted 4 times with ethyl acetate. The ethyl acetate layers were washed with a water/brine mixture 5 times. The aqueous wash layers were back extracted with ethyl acetate twice. The organic layers were combined, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (0 to 100% ethyl acetate in hexane) to give 14.1 g of {4-[(3,4-dinitrophenyl)oxy]phenyl}methanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07939528B2
出典データセットuspto-grants-2011_05
ORD IDord-1e841c2472d34406894f9a6e49077704
出典メモuspto-grants-2011_05