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HRID 964618作成日:2026年10月26日

Sodium Iodide → 1-(3-Nitro-4-phenylmethoxyphenyl)ethanone

https://huagongshe.com/reaction/964618

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物4-Hydroxy-3-NitroacetophenoneHCID 138723—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物1-(3-Nitro-4-phenylmethoxyphenyl)ethanoneHCID 1126572084%

反応条件

温度20 °C

反応手順

To a mechanically stirred DMF (260 mL) suspension of 1-[4-hydroxy-3-nitrophenyl]ethanone (51 g, 282 mmol) and K2CO3 (17 g, 847 mmol) was added benzyl bromide (68 mL, 572 mmol) followed by NaI (47 g, 313 mmol). After stirring overnight at 20° C., an additional 10 mL of benzyl bromide was added and the reaction was stirred for 15 more minutes. The reaction was quenched by the addition of 1.6 L water. The resulting suspension was stirred overnight and then filtered. The collected solids were washed 3×250 mL=750 mL water and dried in vacuo at ~55° C. to give 75 g crude product which was slurried in 1.3 L toluene at ~75° C., filtered hot through a 5.0 μm membrane, concentrated in vacuo to a volume of ~300 mL, diluted with 250 mL heptane, and the suspension cooled from ~60° C. to ambient. After filtration, the collected solids were washed with heptane and dried in vacuo at ~55° C. to give 64 g (84%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05770615
出典データセットuspto-grants-1998_06
ORD IDord-a1277345ecd2461dafe9eaf0610e5c60
出典メモuspto-grants-1998_06